Hobson Prior is currently collaborating with a CRO, who are actively seeking a Head of Quality Assurance to oversee and uphold the highest standards within our clinical research processes. In this pivotal role, you will lead a dedicated team committed to maintaining excellence and driving continuous improvement. Your responsibilities will include ensuring that our operations align with the rigorous standards outlined in Good Clinical Practice (GCP) guidelines and regulations. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Create and put into action a quality assurance strategy to make sure we meet Good Clinical Practice guidelines and regulations. Lead the Quality Assurance team, promoting a culture of excellence, responsibility, and ongoing improvement. Regularly check clinical trial processes, documents, and systems to find areas that don't comply and make necessary changes. Work with different teams to develop and maintain quality management systems that support Good Clinical Practice compliance throughout the organization. Prepare for and manage regulatory inspections, ensuring readiness and compliance with regulatory requirements. Stay updated on changes to Good Clinical Practice regulations and industry standards, and proactively assess the impact on our clinical operations. Train and guide internal stakeholders on Good Clinical Practice requirements, quality standards, and best practices. Act as an expert on Good Clinical Practice compliance matters, providing guidance and support to internal teams and external partners. Requirements Bachelor's degree in a relevant scientific discipline. Experience in a quality assurance role within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with excellent communication, collaboration, and interpersonal skills. Detail-oriented with strong analytical and problem-solving abilities. Proven ability to drive quality assurance initiatives and ensure compliance in a clinical environment. Experience leading regulatory inspections and audits is highly desirable. Apply Now If you're interested in learning more or applying for this opportunity, click "Apply" and upload your CV. For further details or to speak with a life sciences recruitment specialist directly, click "Contact me" at the top of the page. Hobson Prior is a leading life sciences recruiter matching exceptional people with top global positions. Hobson Prior is acting as an Employment Agency for this vacancy. By submitting your details, you confirm you have read our privacy policy. Your data will only be shared with our group at () and third parties listed at (). Hobson Prior are in search of a Validation Specialist in Quality Assurance to join a renowned pharmaceutical corporation. Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. Hobson Prior are on the lookout for a Director for Global QA Laboratories! Hobson Prior are in search of a Validation Specialist in Quality Assurance to join a renowned pharmaceutical corporation. Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. Hobson Prior are on the lookout for a Director for Global QA Laboratories! Hobson Prior are in search of a Validation Specialist in Quality Assurance to join a renowned pharmaceutical corporation. Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. Hobson Prior are on the lookout for a Director for Global QA Laboratories! We don't advertise all of our vacancies online. Register with us and we can let you know the next time your perfect role becomes available, or want to discuss your options with a specialist?
May 17, 2024
Full time
Hobson Prior is currently collaborating with a CRO, who are actively seeking a Head of Quality Assurance to oversee and uphold the highest standards within our clinical research processes. In this pivotal role, you will lead a dedicated team committed to maintaining excellence and driving continuous improvement. Your responsibilities will include ensuring that our operations align with the rigorous standards outlined in Good Clinical Practice (GCP) guidelines and regulations. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Create and put into action a quality assurance strategy to make sure we meet Good Clinical Practice guidelines and regulations. Lead the Quality Assurance team, promoting a culture of excellence, responsibility, and ongoing improvement. Regularly check clinical trial processes, documents, and systems to find areas that don't comply and make necessary changes. Work with different teams to develop and maintain quality management systems that support Good Clinical Practice compliance throughout the organization. Prepare for and manage regulatory inspections, ensuring readiness and compliance with regulatory requirements. Stay updated on changes to Good Clinical Practice regulations and industry standards, and proactively assess the impact on our clinical operations. Train and guide internal stakeholders on Good Clinical Practice requirements, quality standards, and best practices. Act as an expert on Good Clinical Practice compliance matters, providing guidance and support to internal teams and external partners. Requirements Bachelor's degree in a relevant scientific discipline. Experience in a quality assurance role within the pharmaceutical industry. Deep understanding of Good Clinical Practice guidelines, regulations, and standards. Relevant certifications such as RQAP-GLP, RQAP-GCP are desirable. Leadership experience along with excellent communication, collaboration, and interpersonal skills. Detail-oriented with strong analytical and problem-solving abilities. Proven ability to drive quality assurance initiatives and ensure compliance in a clinical environment. Experience leading regulatory inspections and audits is highly desirable. Apply Now If you're interested in learning more or applying for this opportunity, click "Apply" and upload your CV. For further details or to speak with a life sciences recruitment specialist directly, click "Contact me" at the top of the page. Hobson Prior is a leading life sciences recruiter matching exceptional people with top global positions. Hobson Prior is acting as an Employment Agency for this vacancy. By submitting your details, you confirm you have read our privacy policy. Your data will only be shared with our group at () and third parties listed at (). Hobson Prior are in search of a Validation Specialist in Quality Assurance to join a renowned pharmaceutical corporation. Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. Hobson Prior are on the lookout for a Director for Global QA Laboratories! Hobson Prior are in search of a Validation Specialist in Quality Assurance to join a renowned pharmaceutical corporation. Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. Hobson Prior are on the lookout for a Director for Global QA Laboratories! Hobson Prior are in search of a Validation Specialist in Quality Assurance to join a renowned pharmaceutical corporation. Hobson Prior is seeking a dedicated individual for the role of AD Clinical QA Compliance. Hobson Prior are on the lookout for a Director for Global QA Laboratories! We don't advertise all of our vacancies online. Register with us and we can let you know the next time your perfect role becomes available, or want to discuss your options with a specialist?
Hobson Prior International Ltd
Bishop's Stortford, Hertfordshire
Principal Consultant - Clinical (Remote - UK Based) Hobson Prior is seeking a Principal Clinical Consultant with a strong background in clinical development and regulatory affairs. This role will involve providing strategic, technical, and regulatory advice to clients in the development of human medicinal products across a wide range of therapeutic indications. The successful candidate will also contribute to the authorship and review of regulatory documents and provide leadership within the consultancy team. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities For this role you will, provide strategic, technical, and regulatory advice/services to clients in the area of clinical development of human medicinal products. Offer support and advice across a broad range of regulatory activities. Contribute to technical authorship and review of development regulatory documents. Provide technical leadership to other members of the consultancy team. Represent clients in regulatory agency interactions and provide regulatory solutions to agency objections. Requirements A high scientific calibre with a life science focused BSc (or equivalent), and a higher degree in a biomedical field or equivalent (e.g., a life science focused MSc or preferably a PhD). MD qualification would be advantageous but is not essential. Clinical development experience across a range of therapeutic indications/disease areas. Proven ability in defining and delivering creative scientifically driven solutions to technical development and regulatory issues. Experience in negotiation with multinational regulatory authorities including, as a minimum, European, UK and US authorities. Exemplary verbal communication and presentation skills in English. Apply now If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at and those categories of third parties in our privacy policy at We don't advertise all of our vacancies online. Register with us and we can let you know the next time your perfect role becomes available, or want to discuss your options with a specialist?
May 08, 2024
Full time
Principal Consultant - Clinical (Remote - UK Based) Hobson Prior is seeking a Principal Clinical Consultant with a strong background in clinical development and regulatory affairs. This role will involve providing strategic, technical, and regulatory advice to clients in the development of human medicinal products across a wide range of therapeutic indications. The successful candidate will also contribute to the authorship and review of regulatory documents and provide leadership within the consultancy team. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities For this role you will, provide strategic, technical, and regulatory advice/services to clients in the area of clinical development of human medicinal products. Offer support and advice across a broad range of regulatory activities. Contribute to technical authorship and review of development regulatory documents. Provide technical leadership to other members of the consultancy team. Represent clients in regulatory agency interactions and provide regulatory solutions to agency objections. Requirements A high scientific calibre with a life science focused BSc (or equivalent), and a higher degree in a biomedical field or equivalent (e.g., a life science focused MSc or preferably a PhD). MD qualification would be advantageous but is not essential. Clinical development experience across a range of therapeutic indications/disease areas. Proven ability in defining and delivering creative scientifically driven solutions to technical development and regulatory issues. Experience in negotiation with multinational regulatory authorities including, as a minimum, European, UK and US authorities. Exemplary verbal communication and presentation skills in English. Apply now If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at and those categories of third parties in our privacy policy at We don't advertise all of our vacancies online. Register with us and we can let you know the next time your perfect role becomes available, or want to discuss your options with a specialist?
Hobson Prior is on the lookout for a dynamic HR Director to drive business transformation within a global pharmaceutical company. This strategic role involves defining, building, and implementing global HR policies, designing organization and staff development strategies, and managing day-to-day tasks. The successful candidate will be leading an existing HR team, making hands-on leadership a key aspect of this role. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Drive business transformation at a strategic level. Define, build, and implement global HR policies. Design and execute organization and staff development strategies. Manage day-to-day HR tasks and lead an existing HR team. Requirements Over 10 years' experience within the pharmaceutical, biotechnology, and health technology sectors. Global experience, including working with teams in other countries. Proven track record in scaling and transforming businesses. Ability to work in the office 3 days a week. Apply now If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at and those categories of third parties in our privacy policy at We don't advertise all of our vacancies online. Register with us and we can let you know the next time your perfect role becomes available, or want to discuss your options with a specialist?
May 08, 2024
Full time
Hobson Prior is on the lookout for a dynamic HR Director to drive business transformation within a global pharmaceutical company. This strategic role involves defining, building, and implementing global HR policies, designing organization and staff development strategies, and managing day-to-day tasks. The successful candidate will be leading an existing HR team, making hands-on leadership a key aspect of this role. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities Drive business transformation at a strategic level. Define, build, and implement global HR policies. Design and execute organization and staff development strategies. Manage day-to-day HR tasks and lead an existing HR team. Requirements Over 10 years' experience within the pharmaceutical, biotechnology, and health technology sectors. Global experience, including working with teams in other countries. Proven track record in scaling and transforming businesses. Ability to work in the office 3 days a week. Apply now If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By providing your details and submitting this form, you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at and those categories of third parties in our privacy policy at We don't advertise all of our vacancies online. Register with us and we can let you know the next time your perfect role becomes available, or want to discuss your options with a specialist?
Hobson Prior are currently working alongside a fantastic biotech establishment who have an opening for a Good Clinical Practice Compliance Manager to join their team on a contract basis. Our client is focused on converting ground-breaking concepts and findings into remedies for people who suffer from serious diseases. Please note that to be considered for this role you must have the right to work i...... click apply for full job details
Jul 31, 2022
Contractor
Hobson Prior are currently working alongside a fantastic biotech establishment who have an opening for a Good Clinical Practice Compliance Manager to join their team on a contract basis. Our client is focused on converting ground-breaking concepts and findings into remedies for people who suffer from serious diseases. Please note that to be considered for this role you must have the right to work i...... click apply for full job details
Hobson Prior International Ltd
Hoddesdon, Hertfordshire
Hobson Prior are currently seeking for a Brand and Customer Manager to join a brilliant pharmaceutical establishment on a contract basis. Our client is focused on assisting patients and the population. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: For this role, you will be responsible for guiding marketing-led campaigns, guar...... click apply for full job details
Jul 31, 2022
Contractor
Hobson Prior are currently seeking for a Brand and Customer Manager to join a brilliant pharmaceutical establishment on a contract basis. Our client is focused on assisting patients and the population. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: For this role, you will be responsible for guiding marketing-led campaigns, guar...... click apply for full job details
Hobson Prior are seeking for a Bioprocessing Scientist to join a Biotech organisation to be located in London on a permanent basis. Our client is determined to develop treatments who can save patients' lives. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: Perform production processes, following SOPs and GMP practices to manufac...... click apply for full job details
Dec 05, 2021
Full time
Hobson Prior are seeking for a Bioprocessing Scientist to join a Biotech organisation to be located in London on a permanent basis. Our client is determined to develop treatments who can save patients' lives. Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: Perform production processes, following SOPs and GMP practices to manufac...... click apply for full job details
Hobson Prior International Ltd
Cambridge, Cambridgeshire
Hobson Prior are looking to recruit a passionate Research Associate to join our fantastic client on a permanent basis. For more information, please get in touch now! Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: Creating tissue microarrays...... click apply for full job details
Dec 01, 2021
Full time
Hobson Prior are looking to recruit a passionate Research Associate to join our fantastic client on a permanent basis. For more information, please get in touch now! Please note that to be considered for this role you must have the right to work in this location. Key Responsibilities: Creating tissue microarrays...... click apply for full job details
Hobson Prior are currently working with a top pharmaceutical organisation who are focused on the development, manufacturing and commercialising of medicines that will make a real transformation to patients and their family's lives. Our client is seeking a Regulatory Affairs Specialist to join them on a permanent basis. Please note that to be considered for this role you must have the right to work ...... click apply for full job details
Nov 30, 2021
Full time
Hobson Prior are currently working with a top pharmaceutical organisation who are focused on the development, manufacturing and commercialising of medicines that will make a real transformation to patients and their family's lives. Our client is seeking a Regulatory Affairs Specialist to join them on a permanent basis. Please note that to be considered for this role you must have the right to work ...... click apply for full job details