Locum Associate or Senior Editor (Immunology), Nature Communications Location: London, Shanghai or Beijing - hybrid working model Closing date: 28th April, candidates will be considered as they apply. About The Role Do you love science but feel that a career at the bench isn't enough to sate your desire to learn more about the natural world? Do you enjoy reading papers outside your chosen area of research? If the answer is 'yes' to any or all of these questions, you could be the person we're looking for to join the editorial team of Nature Communications. Nature Communications is the leading multidisciplinary Open Access journal, publishing high-quality scientific research. To help us to build on the success of this journal, we're looking for an expert in immunology. The successful candidate will report to the Chief Editor for immunology in the Biological Sciences division. This demanding and intellectually stimulating role is located in one of our offices in London, Beijing or Shanghai on a hybrid working pattern. The position is offered on a full-time, fixed-term maternity cover contract basis. The responsibilities include: Handling original research papers and working closely with other editors on all aspects of the editorial process, including manuscript selection and overseeing peer review. Making well-reasoned editorial decisions on submitted manuscripts in the light of expert advice. Determining the representation of their subject in the journal. Liaising extensively with editors at other journals in the Nature family and with experts in the international scientific community. Attending conferences and visiting research institutions. Commission and edit Reviews, and write Editorials Experience, Skills & Qualifications: A PhD (or equivalent) in a field of immunology. Significant research experience is preferred but not essential. A thorough understanding of recent trends and developments in the field is essential. A passion for science and a thirst to learn more. You must be able to demonstrate the breadth of your interest in scientific research, both within and beyond your specialty. Excellent communication and interpersonal skills and be fluent in English (written and spoken). The ability to read and assess the novelty, context and implications of research submitted to the journal from different areas of this discipline. Be eager to travel and meet scientists worldwide, learn more about them and their research, and help them learn more about us and what we are looking for in the papers we seek to publish. Editorial experience is not required. To apply: Applicants should include a CV and a covering letter explaining their interest in the post. Springer Nature is a Disability Confident Committed Employer and we encourage applications from candidates with disabilities. If you consider yourself to have a disability or learning difficulty and wish to submit your application in an alternative format or would like to discuss reasonable adjustments during the application and interview process, please get in touch either by phone on (0) or by email so we can make any necessary arrangements. If you have any access needs related to disability, neurodivergence or a chronic condition, please contact us so we can make all necessary accommodation. At Springer Nature we value the diversity of our teams. We recognize the many benefits of a diverse workforce with equitable opportunities for everyone. We strive for an inclusive workplace that empowers all our colleagues to thrive. Our search for the best talent fully encompasses and embraces these values and principles. Springer Nature was awarded Diversity Team of the Year at the 2022 British Diversity Awards. Find out more about our DEI work here For more information about career opportunities in Springer Nature please visit
Apr 17, 2024
Full time
Locum Associate or Senior Editor (Immunology), Nature Communications Location: London, Shanghai or Beijing - hybrid working model Closing date: 28th April, candidates will be considered as they apply. About The Role Do you love science but feel that a career at the bench isn't enough to sate your desire to learn more about the natural world? Do you enjoy reading papers outside your chosen area of research? If the answer is 'yes' to any or all of these questions, you could be the person we're looking for to join the editorial team of Nature Communications. Nature Communications is the leading multidisciplinary Open Access journal, publishing high-quality scientific research. To help us to build on the success of this journal, we're looking for an expert in immunology. The successful candidate will report to the Chief Editor for immunology in the Biological Sciences division. This demanding and intellectually stimulating role is located in one of our offices in London, Beijing or Shanghai on a hybrid working pattern. The position is offered on a full-time, fixed-term maternity cover contract basis. The responsibilities include: Handling original research papers and working closely with other editors on all aspects of the editorial process, including manuscript selection and overseeing peer review. Making well-reasoned editorial decisions on submitted manuscripts in the light of expert advice. Determining the representation of their subject in the journal. Liaising extensively with editors at other journals in the Nature family and with experts in the international scientific community. Attending conferences and visiting research institutions. Commission and edit Reviews, and write Editorials Experience, Skills & Qualifications: A PhD (or equivalent) in a field of immunology. Significant research experience is preferred but not essential. A thorough understanding of recent trends and developments in the field is essential. A passion for science and a thirst to learn more. You must be able to demonstrate the breadth of your interest in scientific research, both within and beyond your specialty. Excellent communication and interpersonal skills and be fluent in English (written and spoken). The ability to read and assess the novelty, context and implications of research submitted to the journal from different areas of this discipline. Be eager to travel and meet scientists worldwide, learn more about them and their research, and help them learn more about us and what we are looking for in the papers we seek to publish. Editorial experience is not required. To apply: Applicants should include a CV and a covering letter explaining their interest in the post. Springer Nature is a Disability Confident Committed Employer and we encourage applications from candidates with disabilities. If you consider yourself to have a disability or learning difficulty and wish to submit your application in an alternative format or would like to discuss reasonable adjustments during the application and interview process, please get in touch either by phone on (0) or by email so we can make any necessary arrangements. If you have any access needs related to disability, neurodivergence or a chronic condition, please contact us so we can make all necessary accommodation. At Springer Nature we value the diversity of our teams. We recognize the many benefits of a diverse workforce with equitable opportunities for everyone. We strive for an inclusive workplace that empowers all our colleagues to thrive. Our search for the best talent fully encompasses and embraces these values and principles. Springer Nature was awarded Diversity Team of the Year at the 2022 British Diversity Awards. Find out more about our DEI work here For more information about career opportunities in Springer Nature please visit
ABOUT THE ROLE You will be joining a newly incorporated company founded by Dr. Loïc Roux , OligoTune, as a scientist with expertise in immunology and cancer immunotherapy. Over the last 9 months, Loïc has worked with DSV, devising and de-risking a novel RNA-based approach to overcome immune suppression in the tumour microenvironment. This venture is now close to being launched, and by joining Loïc at this stage, you will be driving the key experimental work required to achieve early stage milestones, optimising the preclinical development of this approach. OligoTune will continue receiving support from the DSV team post-spinout, and in addition, you will be teamed up with our Venture Partner for this opportunity, Dr. Steven Powell, alongside a growing advisory board. THE OPPORTUNITY AREA Immunotherapies, especially antibody-based immune checkpoint inhibitors (ICIs) and CAR-T cell therapy have revolutionised cancer treatment with incredible results in a subset of solid tumours and in blood cancers, respectively. Despite this widely recognised success and paradigm shift in cancer treatment, these therapies still only increase median patient survival by limited degrees, often by only 10-20% vs. chemotherapies, or they only work in selected patient subsets with variable predictability. In addition, the development of resistance mechanisms, such as enhanced immune suppression, is frequent, as a result of selective pressure on the cancer to evade this method of detection by the immune system. This leads to therapeutic resistance initially and, later, recurrence. We are still far from enabling immunotherapies to work across all cancers, or in all patients. Immune suppression is caused by a variety of mechanisms within the tumour microenvironment (TME) of solid tumours, and is a well-known cause for failure of ICIs. The lack of TME-specific cell markers means that targeted approaches (e.g. to inhibit or deplete TME cell types) incur significant autoimmune-like side effects on the same cells in other parts of the body, rendering these therapies intolerable or unusable in a substantial proportion of patients - an issue that typically compounds with combinatorial immunotherapies. WHAT WE ARE BUILDING In collaboration with our partner Cancer Research Horizons, we are seeking to build the 'holy grail' company, solving these above challenges by simultaneously reprogramming multiple problematic cell types in the tumour microenvironment, while preventing systemic toxicities associated with current treatments. We believe we can build technology that can revert the immune suppressive environment of solid tumours and transform them into a susceptible state where the full power of ICIs can be unleashed - even in patients who would otherwise not respond (or be eligible for) conventional ICI therapies. The collaboration with Cancer Research Horizons Therapeutic Innovation brings a highly-skilled team of scientific leaders and hands-on experts to drive the creation of this venture and realise a streamlined pathway for this therapeutic approach to the clinic. DSV will provide ongoing support in venture creation and growth throughout the process, and experimental work will be supported through in-kind contributions at Cancer Research Horizons' state-of-the-art research facilities in Cambridge, UK. We are looking for a passionate and motivated scientist with strong immunological expertise and track-record in immunology or immuno-oncology, to drive forward the science of this early-stage biotech. The successful candidate will be a key player in: Driving the strategic direction of the immuno-oncology aspects of the experimental work plan; Designing, refining and optimising the experimental work plan and scientific process; Orchestrating the development of cutting-edge oligonucleotide therapeutics for critical in vitro and ex vivo translational studies in order to assess efficacy, toxicology and PK/PD profiles of those drugs in the context of our technology; Planning in vivo biodistribution and efficacy studies; Ensuring that all techniques are updated with the latest advancements in the field; Guiding the development and integration of new assays and technologies, to continuously improve our technology; Streamlining the workflow to adhere to timelines and budgets; Ensuring data quality and integrity, to align with objectives and deadlines; Crafting compelling data packages and presentations for investor conversations. WHO SHOULD APPLY Essential (must-have): You have a PhD in immunology or immuno-oncology (or MRes + 5 years of relevant work experience). You are driven by unsolved challenges in medicine, especially oncology and immunotherapy, and have the ambition to work with a team to build new solutions resulting in curative therapies A deep biological understanding of immune cell biology, particularly immune cells present within the tumour microenvironment Extensive hands-on experience in functional immunological assays, particularly with tumour microenvironment immune cell types (ie. T cells, Tregs, macrophages, others). A deep understanding of cancer immunotherapy mechanisms and associated challenges at the biological, clinical and technical levels You are innovative, creative, and guided by first-principles thinking Preferred (nice-to-have): Track record of high quality publications in the field, or thought leadership in the field Bioinformatics and data analysis skills Drug discovery or (pre-)clinical development expertise OUR OFFER: Salary benchmarked against similar stage companies, with an attractive share option plan for early hire We provide optimised, purpose-built, proprietary tools, resources and processes to help create high-impact ventures from scratch, using our venture creation methodology. We draw on opportunity area specific know-how provided by our network of Partners and Advisors; DSV provide continuous support after post spin-out, including fundraising, commercial partnerships, recruitment and team-building (amongst other things); plus There are dozens of Founders currently at DSV across sectors working collaboratively and supporting one another - a unique resource to draw on. WHO YOU'LL BE JOINING: You will be joining Dr. Loïc Roux , an accomplished scientist whose expertise sits within biotechnology, drug discovery and development, pharmacokinetic and translational science with a focus on design, manufacture, formulation and pre-clinical development of nucleic acid therapeutics. His experience comes from prestigious institutions in the nucleic acid field including The RNA Therapeutics Institute at UMass Med School and Oxford University, where he pushed forward research programs in neurodegenerative and neuromuscular diseases. After a position as principal scientist at PepGen Ltd promoting a peptide delivery platform for nucleic acid delivery, he contributed to building and establishing NATA, a new UKRI initiative aiming to promote the development of nucleic acid therapeutics. He then moved back to industry as Director of Lead Development for OchreBio, a Phenomics-led RNA medicines company developing the next-generation of RNA therapeutics for chronic liver diseases where he built oligonucleotide and new modalities chemistry capabilities, alongside efficacy and toxicity biology capabilities, to collaborate on programs including target screens, translational model development from primary cells to human organs, delivery methodology for specific cell types including HCC cancer cells, and led innovation programs for IP generation and scientific strategy. ABOUT DSV Deep Science Ventures is creating a future in which both humans and the planet can thrive. We use our unique venture creation process to create, spin-out and invest into science companies, combining available scientific knowledge and founder-type scientists into high-impact ventures. We operate in 4 sectors: Pharmaceuticals, Climate, Agriculture and Computation, tackling the challenges defining those areas by taking a first principles approach and partnering with leading institutions.
Apr 15, 2024
Full time
ABOUT THE ROLE You will be joining a newly incorporated company founded by Dr. Loïc Roux , OligoTune, as a scientist with expertise in immunology and cancer immunotherapy. Over the last 9 months, Loïc has worked with DSV, devising and de-risking a novel RNA-based approach to overcome immune suppression in the tumour microenvironment. This venture is now close to being launched, and by joining Loïc at this stage, you will be driving the key experimental work required to achieve early stage milestones, optimising the preclinical development of this approach. OligoTune will continue receiving support from the DSV team post-spinout, and in addition, you will be teamed up with our Venture Partner for this opportunity, Dr. Steven Powell, alongside a growing advisory board. THE OPPORTUNITY AREA Immunotherapies, especially antibody-based immune checkpoint inhibitors (ICIs) and CAR-T cell therapy have revolutionised cancer treatment with incredible results in a subset of solid tumours and in blood cancers, respectively. Despite this widely recognised success and paradigm shift in cancer treatment, these therapies still only increase median patient survival by limited degrees, often by only 10-20% vs. chemotherapies, or they only work in selected patient subsets with variable predictability. In addition, the development of resistance mechanisms, such as enhanced immune suppression, is frequent, as a result of selective pressure on the cancer to evade this method of detection by the immune system. This leads to therapeutic resistance initially and, later, recurrence. We are still far from enabling immunotherapies to work across all cancers, or in all patients. Immune suppression is caused by a variety of mechanisms within the tumour microenvironment (TME) of solid tumours, and is a well-known cause for failure of ICIs. The lack of TME-specific cell markers means that targeted approaches (e.g. to inhibit or deplete TME cell types) incur significant autoimmune-like side effects on the same cells in other parts of the body, rendering these therapies intolerable or unusable in a substantial proportion of patients - an issue that typically compounds with combinatorial immunotherapies. WHAT WE ARE BUILDING In collaboration with our partner Cancer Research Horizons, we are seeking to build the 'holy grail' company, solving these above challenges by simultaneously reprogramming multiple problematic cell types in the tumour microenvironment, while preventing systemic toxicities associated with current treatments. We believe we can build technology that can revert the immune suppressive environment of solid tumours and transform them into a susceptible state where the full power of ICIs can be unleashed - even in patients who would otherwise not respond (or be eligible for) conventional ICI therapies. The collaboration with Cancer Research Horizons Therapeutic Innovation brings a highly-skilled team of scientific leaders and hands-on experts to drive the creation of this venture and realise a streamlined pathway for this therapeutic approach to the clinic. DSV will provide ongoing support in venture creation and growth throughout the process, and experimental work will be supported through in-kind contributions at Cancer Research Horizons' state-of-the-art research facilities in Cambridge, UK. We are looking for a passionate and motivated scientist with strong immunological expertise and track-record in immunology or immuno-oncology, to drive forward the science of this early-stage biotech. The successful candidate will be a key player in: Driving the strategic direction of the immuno-oncology aspects of the experimental work plan; Designing, refining and optimising the experimental work plan and scientific process; Orchestrating the development of cutting-edge oligonucleotide therapeutics for critical in vitro and ex vivo translational studies in order to assess efficacy, toxicology and PK/PD profiles of those drugs in the context of our technology; Planning in vivo biodistribution and efficacy studies; Ensuring that all techniques are updated with the latest advancements in the field; Guiding the development and integration of new assays and technologies, to continuously improve our technology; Streamlining the workflow to adhere to timelines and budgets; Ensuring data quality and integrity, to align with objectives and deadlines; Crafting compelling data packages and presentations for investor conversations. WHO SHOULD APPLY Essential (must-have): You have a PhD in immunology or immuno-oncology (or MRes + 5 years of relevant work experience). You are driven by unsolved challenges in medicine, especially oncology and immunotherapy, and have the ambition to work with a team to build new solutions resulting in curative therapies A deep biological understanding of immune cell biology, particularly immune cells present within the tumour microenvironment Extensive hands-on experience in functional immunological assays, particularly with tumour microenvironment immune cell types (ie. T cells, Tregs, macrophages, others). A deep understanding of cancer immunotherapy mechanisms and associated challenges at the biological, clinical and technical levels You are innovative, creative, and guided by first-principles thinking Preferred (nice-to-have): Track record of high quality publications in the field, or thought leadership in the field Bioinformatics and data analysis skills Drug discovery or (pre-)clinical development expertise OUR OFFER: Salary benchmarked against similar stage companies, with an attractive share option plan for early hire We provide optimised, purpose-built, proprietary tools, resources and processes to help create high-impact ventures from scratch, using our venture creation methodology. We draw on opportunity area specific know-how provided by our network of Partners and Advisors; DSV provide continuous support after post spin-out, including fundraising, commercial partnerships, recruitment and team-building (amongst other things); plus There are dozens of Founders currently at DSV across sectors working collaboratively and supporting one another - a unique resource to draw on. WHO YOU'LL BE JOINING: You will be joining Dr. Loïc Roux , an accomplished scientist whose expertise sits within biotechnology, drug discovery and development, pharmacokinetic and translational science with a focus on design, manufacture, formulation and pre-clinical development of nucleic acid therapeutics. His experience comes from prestigious institutions in the nucleic acid field including The RNA Therapeutics Institute at UMass Med School and Oxford University, where he pushed forward research programs in neurodegenerative and neuromuscular diseases. After a position as principal scientist at PepGen Ltd promoting a peptide delivery platform for nucleic acid delivery, he contributed to building and establishing NATA, a new UKRI initiative aiming to promote the development of nucleic acid therapeutics. He then moved back to industry as Director of Lead Development for OchreBio, a Phenomics-led RNA medicines company developing the next-generation of RNA therapeutics for chronic liver diseases where he built oligonucleotide and new modalities chemistry capabilities, alongside efficacy and toxicity biology capabilities, to collaborate on programs including target screens, translational model development from primary cells to human organs, delivery methodology for specific cell types including HCC cancer cells, and led innovation programs for IP generation and scientific strategy. ABOUT DSV Deep Science Ventures is creating a future in which both humans and the planet can thrive. We use our unique venture creation process to create, spin-out and invest into science companies, combining available scientific knowledge and founder-type scientists into high-impact ventures. We operate in 4 sectors: Pharmaceuticals, Climate, Agriculture and Computation, tackling the challenges defining those areas by taking a first principles approach and partnering with leading institutions.
Site Name: UK - London - Brentford Posted Date: Sep 9 2022 Join the GSK Industrial Placement UK Programme as an Associate Clinical Development Scientist:Help us get ahead of disease together. Education required: Undergraduate degree from an accredited university, preferably in Life Sciences. Other requirements: You will have completed a minimum of 2 years of your undergraduate degree but will not have graduated at the start of your placement. You must be enrolled at a UK university for the duration of your placement. Language requirement: Written and spoken fluency in English Expected Start date: 4th September 2023 Duration: 1 year (approximately) Location: GSK House - Brentford, Stevenage, and Addenbrookes Hospital GSK CUC. Application deadline: Friday 14th October 2022. We will close this vacancy when we have enough applications, so we recommend that you apply as soon as you can so your application can be considered. Proposed Assessment / Interview Dates: The majority of R&D interviews will take place in the first two weeks of November Salary: A salary of £22,500, plus a bonus (GSK House - Brentford) A salary of £21,000, plus a bonus (Stevenage and Addenbrookes Hospital) Please read below about the 2 different positions we are recruiting for across our Associate Clinical Development Scientist Industrial Placements. Please note, these are distinct placements and so when you apply you will be able to select preferences of where you would like to be placed if successful. We will accommodate your preference where possible. Role 1 - Associate Clinical Development Scientist (Study Management) Location: GSK House or Stevenage Within this role your day-to-day responsibilities will be involved in the testing of new medicines in humans. The role holder will provide project management, operational and technical support to the Study Delivery Leads (SDL) and study teams. This will include: Support study set up and project management activities Support and assist coordination of the required ethics application of designated studies. Focus on study set- up and operational project management and close out activities. Working with your SDL your responsibilities may include but are not limited to: Operational delivery of clinical studies (including, for example: feasibility assessments, overseeing subcontractor's performance, recruitment tracking) Preparation of high-quality scientific materials relating to clinical trials (including, for example: contributing to clinical study protocols, procedures manuals, information and consent forms) Attendance at and contribution to clinical study team meetings. Review of data and writing of associated reports. Assist with planning and tracking of study timelines and budgets. Co-ordinate key study activities such as study documentation filing, study supplies and investigator meetings. Participating in scientific discussions relating to the design of clinical studies You may also be asked to assist with other departmental activities that are not study related. Role 2 - Associate Clinical Development Scientist (GSK Clinical Unit Cambridge, CUC) Location: GSK Clinical Unit Cambridge, Addenbrookes Hospital This role is based in GSK's Phase 1 Clinical unit situated within Addenbrookes Hospital. The role holder will provide project management, operational and technical support to the Clinical Development Managers (CDM) and study teams. This will include: Support study set up and project management activities Support and assist coordination of the required ethics application of designated studies. Focus on study set- up and operational project management and close out activities. Working with the CDM team you will learn: To ensure compliance with regulatory and ethical standards. Maintain accurate and complete study records consistent with company policy and legal and regulatory requirements. Site file maintenance to ensure accurate maintenance of study records for monitoring and inspection-readiness of the site investigator file. Support study scheduling, management of bed occupancy spreadsheet and planning clinical timelines Develop and maintain study budgets. Identify and implement process improvements. Team leadership, management and communication, including meeting management with the unit and GSK study teams. Support the day to day management and running of clinical trials, supporting the clinical teams. Who are we looking for? A keen passion for clinical development - tell us your hobbies or interests that are connected to clinical development, R&D, the commercial world and the biopharma industry Appetite to build strong relationships with key stakeholders Adaptability to change and working under pressure Excellent communication skills that help you influence Strong problem-solving skills driven by curiosity You enjoy learning in action and confidence You are a keen learner The ability to prioritise What do we offer you? A salary of £22,500, plus a bonus (GSK House - Brentford) or salary of £21,000, plus a bonus (Stevenage and Addenbrookes Hospital) Access to GSK resources, including employee assistance programmes, private healthcare and well-being programs and pension plan membership On-the-job experience and informal training and development, delivered through a mixture of coaching, mentoring, and training programs A GSK placement which gives you the opportunity to take on a real role with genuine impact You will join a GSK Industrial Placement community of over 250 students across the UK and business areas Access to LinkedIn groups to enable the new Industrial Placement community to network and connect before start date For R&D placements you will also be enrolled in several GSK internal courses as part of company policy such as data integrity, use of internal electronic lab book, laboratory safety rules. Within R&D you will have the opportunity to attend seminars by GSK scientists, which run throughout the year and comprise of a wide range of areas within drug discovery. Please read above about the 2 different positions we are recruiting for across our Associate Clinical Development Scientist Industrial Placements. Please note, these are distinct placements and so when you apply you will be able to select preferences of where you would like to be placed if successful. We will accommodate your preference where possible. Are you looking to gain valuable real world work experience and help positively impact the lives of others GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. A GSK internship offers you the opportunity to kickstart your career - to take on a real role with genuine impact. You'll take on challenging tasks within live projects or assignments. You'll also get to learn from others in your team and other parts of GSK whilst developing your skills and gaining valuable experience for wherever the future takes you. Inspired to help us get ahead together? Apply for an Associate Clinical Development Scientist Industrial Placement role at GSK today! Our approach to R&D focuses on science related to the prevention and treatment of disease with vaccines, specialty and general medicines. We focus on science of the immune system, human genetics and advanced technologies to impact health at scale. Our pipeline currently comprises of more than 60vaccines and medicines across four core therapeutic areas including oncology, infectious diseases, immunology / respiratory and HIV. Find out more: Our approach to R&D . Let's do this! This opportunity has the following recruitment stages you must successfully pass to be offered a placement year with GSK for 2023: 1. Eligibility Form 2. World of GSK Online Assessment 3. Application Form 4. Virtual Assessment Centre or Virtual Interview You'll find hints, tips and guidance on our recruitment process on our website - Apply now for our Early Talent programmes GSK We will close this vacancy when we have enough applications, so we recommend that you apply as soon as you can so your application can be considered. You can learn more about GSK and our careers here . Apply now! We're 100% open to ALL people We're 100% open to all talent - whatever your gender, marital status, religion, age, colour, race, sexual orientation, nationality, learning difference or disability. We want to recruit the right people for GSK from the widest possible backgrounds, so we can better serve the diversity of our patients and also because it's the right thing to do. You can learn more about Inclusion and diversity at GSK here . Need help with your application? Please email us at or call is on and let us know how we can help you. ..... click apply for full job details
Sep 24, 2022
Full time
Site Name: UK - London - Brentford Posted Date: Sep 9 2022 Join the GSK Industrial Placement UK Programme as an Associate Clinical Development Scientist:Help us get ahead of disease together. Education required: Undergraduate degree from an accredited university, preferably in Life Sciences. Other requirements: You will have completed a minimum of 2 years of your undergraduate degree but will not have graduated at the start of your placement. You must be enrolled at a UK university for the duration of your placement. Language requirement: Written and spoken fluency in English Expected Start date: 4th September 2023 Duration: 1 year (approximately) Location: GSK House - Brentford, Stevenage, and Addenbrookes Hospital GSK CUC. Application deadline: Friday 14th October 2022. We will close this vacancy when we have enough applications, so we recommend that you apply as soon as you can so your application can be considered. Proposed Assessment / Interview Dates: The majority of R&D interviews will take place in the first two weeks of November Salary: A salary of £22,500, plus a bonus (GSK House - Brentford) A salary of £21,000, plus a bonus (Stevenage and Addenbrookes Hospital) Please read below about the 2 different positions we are recruiting for across our Associate Clinical Development Scientist Industrial Placements. Please note, these are distinct placements and so when you apply you will be able to select preferences of where you would like to be placed if successful. We will accommodate your preference where possible. Role 1 - Associate Clinical Development Scientist (Study Management) Location: GSK House or Stevenage Within this role your day-to-day responsibilities will be involved in the testing of new medicines in humans. The role holder will provide project management, operational and technical support to the Study Delivery Leads (SDL) and study teams. This will include: Support study set up and project management activities Support and assist coordination of the required ethics application of designated studies. Focus on study set- up and operational project management and close out activities. Working with your SDL your responsibilities may include but are not limited to: Operational delivery of clinical studies (including, for example: feasibility assessments, overseeing subcontractor's performance, recruitment tracking) Preparation of high-quality scientific materials relating to clinical trials (including, for example: contributing to clinical study protocols, procedures manuals, information and consent forms) Attendance at and contribution to clinical study team meetings. Review of data and writing of associated reports. Assist with planning and tracking of study timelines and budgets. Co-ordinate key study activities such as study documentation filing, study supplies and investigator meetings. Participating in scientific discussions relating to the design of clinical studies You may also be asked to assist with other departmental activities that are not study related. Role 2 - Associate Clinical Development Scientist (GSK Clinical Unit Cambridge, CUC) Location: GSK Clinical Unit Cambridge, Addenbrookes Hospital This role is based in GSK's Phase 1 Clinical unit situated within Addenbrookes Hospital. The role holder will provide project management, operational and technical support to the Clinical Development Managers (CDM) and study teams. This will include: Support study set up and project management activities Support and assist coordination of the required ethics application of designated studies. Focus on study set- up and operational project management and close out activities. Working with the CDM team you will learn: To ensure compliance with regulatory and ethical standards. Maintain accurate and complete study records consistent with company policy and legal and regulatory requirements. Site file maintenance to ensure accurate maintenance of study records for monitoring and inspection-readiness of the site investigator file. Support study scheduling, management of bed occupancy spreadsheet and planning clinical timelines Develop and maintain study budgets. Identify and implement process improvements. Team leadership, management and communication, including meeting management with the unit and GSK study teams. Support the day to day management and running of clinical trials, supporting the clinical teams. Who are we looking for? A keen passion for clinical development - tell us your hobbies or interests that are connected to clinical development, R&D, the commercial world and the biopharma industry Appetite to build strong relationships with key stakeholders Adaptability to change and working under pressure Excellent communication skills that help you influence Strong problem-solving skills driven by curiosity You enjoy learning in action and confidence You are a keen learner The ability to prioritise What do we offer you? A salary of £22,500, plus a bonus (GSK House - Brentford) or salary of £21,000, plus a bonus (Stevenage and Addenbrookes Hospital) Access to GSK resources, including employee assistance programmes, private healthcare and well-being programs and pension plan membership On-the-job experience and informal training and development, delivered through a mixture of coaching, mentoring, and training programs A GSK placement which gives you the opportunity to take on a real role with genuine impact You will join a GSK Industrial Placement community of over 250 students across the UK and business areas Access to LinkedIn groups to enable the new Industrial Placement community to network and connect before start date For R&D placements you will also be enrolled in several GSK internal courses as part of company policy such as data integrity, use of internal electronic lab book, laboratory safety rules. Within R&D you will have the opportunity to attend seminars by GSK scientists, which run throughout the year and comprise of a wide range of areas within drug discovery. Please read above about the 2 different positions we are recruiting for across our Associate Clinical Development Scientist Industrial Placements. Please note, these are distinct placements and so when you apply you will be able to select preferences of where you would like to be placed if successful. We will accommodate your preference where possible. Are you looking to gain valuable real world work experience and help positively impact the lives of others GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together. Getting ahead means preventing disease as well as treating it, and we aim to impact the health of 2.5 billion people around the world in the next 10 years. A GSK internship offers you the opportunity to kickstart your career - to take on a real role with genuine impact. You'll take on challenging tasks within live projects or assignments. You'll also get to learn from others in your team and other parts of GSK whilst developing your skills and gaining valuable experience for wherever the future takes you. Inspired to help us get ahead together? Apply for an Associate Clinical Development Scientist Industrial Placement role at GSK today! Our approach to R&D focuses on science related to the prevention and treatment of disease with vaccines, specialty and general medicines. We focus on science of the immune system, human genetics and advanced technologies to impact health at scale. Our pipeline currently comprises of more than 60vaccines and medicines across four core therapeutic areas including oncology, infectious diseases, immunology / respiratory and HIV. Find out more: Our approach to R&D . Let's do this! This opportunity has the following recruitment stages you must successfully pass to be offered a placement year with GSK for 2023: 1. Eligibility Form 2. World of GSK Online Assessment 3. Application Form 4. Virtual Assessment Centre or Virtual Interview You'll find hints, tips and guidance on our recruitment process on our website - Apply now for our Early Talent programmes GSK We will close this vacancy when we have enough applications, so we recommend that you apply as soon as you can so your application can be considered. You can learn more about GSK and our careers here . Apply now! We're 100% open to ALL people We're 100% open to all talent - whatever your gender, marital status, religion, age, colour, race, sexual orientation, nationality, learning difference or disability. We want to recruit the right people for GSK from the widest possible backgrounds, so we can better serve the diversity of our patients and also because it's the right thing to do. You can learn more about Inclusion and diversity at GSK here . Need help with your application? Please email us at or call is on and let us know how we can help you. ..... click apply for full job details
Labcorp Drug Development
Huntingdon, Cambridgeshire
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people's lives. Join us in our pursuit of answers. Apprenticeship Program: Exciting Opportunity to be part of the Labcorp Drug Development 2022 Apprenticeship Program in the Clinical Pathology Services team in Huntingdon, Cambridgeshire. As an Apprentice Laboratory Technician within Labcorp Drug Development, you will play an integral role in supporting all aspects of laboratory and study support functions for our testing and development work. Following a comprehensive induction process and carefully-tailored training program, you will acquire a comprehensive knowledge of all aspects of clinical trials and bringing miracles of medicine to market. Capitalize on a dedicated training and development program that will support your scientific and professional career aspirations, and take pride in delivering scientific work that helps save the lives of millions of people around the world. Clinical Pathology Services - Provides lab safety assessment for toxicology studies by analysing bloods and urines on a variety of automated chemistry and haematology analysers whilst also utilising a range of manual techniques to obtain data. Analysis is performed by CPS throughout a study on specific timed/dated occasions for the purposes of demonstrating safety and efficacy of client test articles. The assessments performed by CPS are required by all regulatory governing bodies associated with the release to market of new or modified medicines. CPS has a variety of skill sets required from study set up, sample management, lab technicians and scientists. In depth training is provided to ensure high GLP and data integrity standards are adhered too. As an Apprentice Lab Technician, you will be receiving and preparing samples for not only the CPS department but also those for Immunology and Immunotoxicology and Bioanalysis, as well as learning lab technician duties to support the CPS laboratory. Job Purpose: Responsibilities include- The receipt, processing, storage, disposal and tracking of all samples into the division. You will learn the following: Routine and one-off laboratory testing and how to perform a variety of technical laboratory techniques; Work both individually and as part of the laboratory team; Work with minimum supervision, taking responsibility for the quality and accuracy of the work that is undertaken; Work safely in the laboratory, maintaining excellent housekeeping whilst following appropriate safety, environment and risk management systems; Ensure the laboratory is well-stocked and resourced and be able to maintain good accurate written records of work carried out; Follow quality procedures to meet the requirements of quality standards relevant to the workplace; Develop and apply your theoretical knowledge of relevant science and technology; What you'll receive: You'll undertake an Advanced Apprenticeship in Laboratory Technician over the course of 24 months, You will study for a Level 4 Science Qualification An IOSH Managing Safely certificate A chance to Act as an Ambassador across Cambridgeshire for Science roles, A generous benefits and holiday package Progression opportunities and a chance to work on ground breaking trials Minimum Criteria An A-level in Biology or Chemistry preferred but not essential, or relevant work Experience or a level 3 science based qualification, A passion for science, A willingness to learn, Able to work independently as well as part of a team, Great attention to detail, Good communication skills Start date: September 2022 Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .
Aug 01, 2022
Full time
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people's lives. Join us in our pursuit of answers. Apprenticeship Program: Exciting Opportunity to be part of the Labcorp Drug Development 2022 Apprenticeship Program in the Clinical Pathology Services team in Huntingdon, Cambridgeshire. As an Apprentice Laboratory Technician within Labcorp Drug Development, you will play an integral role in supporting all aspects of laboratory and study support functions for our testing and development work. Following a comprehensive induction process and carefully-tailored training program, you will acquire a comprehensive knowledge of all aspects of clinical trials and bringing miracles of medicine to market. Capitalize on a dedicated training and development program that will support your scientific and professional career aspirations, and take pride in delivering scientific work that helps save the lives of millions of people around the world. Clinical Pathology Services - Provides lab safety assessment for toxicology studies by analysing bloods and urines on a variety of automated chemistry and haematology analysers whilst also utilising a range of manual techniques to obtain data. Analysis is performed by CPS throughout a study on specific timed/dated occasions for the purposes of demonstrating safety and efficacy of client test articles. The assessments performed by CPS are required by all regulatory governing bodies associated with the release to market of new or modified medicines. CPS has a variety of skill sets required from study set up, sample management, lab technicians and scientists. In depth training is provided to ensure high GLP and data integrity standards are adhered too. As an Apprentice Lab Technician, you will be receiving and preparing samples for not only the CPS department but also those for Immunology and Immunotoxicology and Bioanalysis, as well as learning lab technician duties to support the CPS laboratory. Job Purpose: Responsibilities include- The receipt, processing, storage, disposal and tracking of all samples into the division. You will learn the following: Routine and one-off laboratory testing and how to perform a variety of technical laboratory techniques; Work both individually and as part of the laboratory team; Work with minimum supervision, taking responsibility for the quality and accuracy of the work that is undertaken; Work safely in the laboratory, maintaining excellent housekeeping whilst following appropriate safety, environment and risk management systems; Ensure the laboratory is well-stocked and resourced and be able to maintain good accurate written records of work carried out; Follow quality procedures to meet the requirements of quality standards relevant to the workplace; Develop and apply your theoretical knowledge of relevant science and technology; What you'll receive: You'll undertake an Advanced Apprenticeship in Laboratory Technician over the course of 24 months, You will study for a Level 4 Science Qualification An IOSH Managing Safely certificate A chance to Act as an Ambassador across Cambridgeshire for Science roles, A generous benefits and holiday package Progression opportunities and a chance to work on ground breaking trials Minimum Criteria An A-level in Biology or Chemistry preferred but not essential, or relevant work Experience or a level 3 science based qualification, A passion for science, A willingness to learn, Able to work independently as well as part of a team, Great attention to detail, Good communication skills Start date: September 2022 Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement .