Global Clinical Program Manager for Biotech Regulatory Affairs
4 days ago
Lifelancer is a talent-hiring platform in Life Sciences, Pharma, and IT. We connect talented professionals with opportunities in pharma, biotech, health sciences, healthtech, and IT domains.
Job Title: Global Clinical Program Manager for Biotech Regulatory AffairsWe are seeking a highly skilled Global Clinical Program Manager for our Regulatory Affairs team. As a key member of our team, you will be responsible for managing clinical programs and ensuring compliance with regulatory requirements.
Responsibilities:- Develop and implement global clinical trial strategies to meet business objectives
- Collaborate with cross-functional teams to ensure seamless execution of clinical trials
- Maintain awareness of regulatory developments and updates in the life sciences industry
- Degree in Law or related field
- Proven experience in regulatory affairs, preferably in a biotech/pharmaceutical company
- Excellent communication and project management skills
- A competitive salary of £80,000 - £110,000 per annum
- A dynamic and supportive work environment
- Ongoing training and development opportunities
This role can be based in our Cambridge office, with occasional travel required to other locations within the UK and abroad.
Apply now to take your career to the next level
-
Regulatory Affairs Expert
5 days ago
Cambridge, Cambridgeshire, United Kingdom MoonLake Immunotherapeutics Full timeJoin MoonLake Immunotherapeutics as an Associate Director of Regulatory Affairs to spearhead innovative global regulatory strategies for sonelokimab lead indication(s).About the RoleCreate and execute cutting-edge regulatory plans to drive product development and approval, aligning with the company's global business strategy.As a key member of our team, you...
-
Global Regulatory Affairs Director
5 days ago
Cambridge, Cambridgeshire, United Kingdom MoonLake Immunotherapeutics Full timeJob OverviewMoonLake Immunotherapeutics seeks a highly skilled Global Regulatory Affairs Director to lead the development and implementation of innovative global regulatory strategies for sonelokimab lead indication(s).This role will be responsible for regulatory aspects related to product development and approval, aligning with the global business strategy...
-
Cambridge, Cambridgeshire, United Kingdom MoonLake Immunotherapeutics Full timeJob DescriptionMoonLake Immunotherapeutics is seeking a skilled Regulatory Affairs Strategist to develop and deliver innovative global regulatory strategies for sonelokimab lead indication(s). This role will be an integral part of our team, responsible for regulatory aspects related to product development and approval.We are looking for a candidate with a...
-
Regulatory Affairs Director
1 month ago
Cambridge, Cambridgeshire, United Kingdom MoonLake Immunotherapeutics Full timeJob Overview At MoonLake Immunotherapeutics, we are seeking an experienced Associate Director of Regulatory Affairs to join our team. As a key member of our regulatory affairs team, you will play a critical role in developing and delivering innovative global regulatory strategies for our sonelokimab lead indication(s). Responsibilities * Collaborate with...
-
Regulatory Affairs Director
2 weeks ago
Cambridge, Cambridgeshire, United Kingdom Lifelancer Full timeJob DescriptionCompany Overview: Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT.We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains. Our mission is to provide innovative solutions for businesses and professionals in the industry.SalaryThe estimated salary for this position...
-
Regulatory Affairs Director
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom MoonLake Immunotherapeutics Full timeJob OverviewMoonLake Immunotherapeutics is seeking an experienced Associate Director to lead the development and implementation of innovative global regulatory strategies for sonelokimab lead indication(s).This role will be responsible for regulatory aspects related to product development and approval, in alignment with the global business strategy and in...
-
Director, Global Regulatory Strategy
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom MoonLake Immunotherapeutics Full timeJob OverviewMoonLake Immunotherapeutics is seeking a highly skilled Director, Global Regulatory Strategy to join our team. This is a critical role that will play a key part in shaping our regulatory strategy and ensuring the successful development and approval of our novel investigational Nanobody.The ideal candidate will have a strong background in...
-
Senior Regulatory Affairs Director
20 hours ago
Cambridge, Cambridgeshire, United Kingdom Lifelancer Full timeRegulatory Affairs Director Job OverviewWe are seeking a highly skilled Regulatory Affairs Director to join our team at Lifelancer. As a key member of our organization, you will be responsible for developing and delivering innovative global regulatory strategies for sonelokimab lead indication(s).About the RoleThis is an exciting opportunity to work with a...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeAbout the RoleWe are seeking a highly skilled Regulatory Affairs Director to join our team at Gilead Sciences International, Ltd. as a Director, Global Regulatory Affairs, Precision Medicine. This is a unique opportunity to develop and execute Precision Medicine regulatory strategies in alignment with the drug global regulatory strategy in collaboration with...
-
Regulatory Affairs Project Manager
1 week ago
Cambridge, Cambridgeshire, United Kingdom ProductLife Group Full timeProductLife Group is seeking a Regulatory Affairs Project ManagerWe are looking for an experienced professional to lead our Regulatory Affairs outsourcing projects/programs in the UK. The ideal candidate will have a deep understanding of EU RA regulations and be able to coordinate multiple projects simultaneously.About UsAt ProductLife Group, we pride...
-
Senior Global Regulatory Affairs Manager
4 days ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences Full timeJob Overview:At Gilead Sciences, we're dedicated to creating a healthier world for all people. We're seeking a skilled Senior Global Regulatory Affairs Manager to join our team and contribute to the development of life-changing scientific innovations.As a key member of our Global Regulatory Affairs team, you will play a critical role in shaping our...
-
Global Regulatory Affairs Labeling Director
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob Title: Global Regulatory Affairs Labeling DirectorJob Summary:Gilead Sciences International, Ltd. is seeking a highly experienced Global Regulatory Affairs Labeling Director to lead our Global Regulatory Affairs Labeling organization. The successful candidate will be responsible for developing and implementing global labeling strategies, ensuring...
-
Regulatory Affairs Manager
2 weeks ago
Cambridge, Cambridgeshire, United Kingdom Bicycle Therapeutics Full timeCompany OverviewBicycle Therapeutics is a cutting-edge company that focuses on revolutionizing the field of pharmaceuticals through innovative technologies and groundbreaking research.We are committed to building a diverse workforce that reflects the communities we serve, fostering an inclusive environment where everyone can thrive.SalaryThe estimated salary...
-
Global Regulatory Affairs Liaison
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob SummaryGilead Sciences International, Ltd. is seeking a highly skilled Global Regulatory Affairs Liaison to join our team. As a key member of our Global Regulatory Affairs organization, you will play a critical role in ensuring the successful development and approval of our medicinal products.Key ResponsibilitiesDevelop and implement regulatory...
-
Global Regulatory Affairs Leader
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeJob Title: Global Regulatory Affairs LeaderJob Summary: Gilead Sciences International, Ltd. is seeking a highly experienced Global Regulatory Affairs Leader to lead our Global Regulatory Affairs Labeling organization.About the Role:Lead the development and implementation of global labeling strategies to ensure compliance with regulatory requirements.Oversee...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences, Inc. Full timeJob Description:Gilead Sciences, Inc. is seeking a highly skilled and experienced professional to lead our Regulatory Affairs Business Operations team. As the Global Regulatory Affairs Business Operations Lead, you will be responsible for developing and implementing global regulatory affairs infrastructure, compliance, process, and capability development.Key...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeGilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs Director to oversee regulatory activities in the Gilead Patient Solutions region.About the RoleThis exciting opportunity allows you to leverage your expertise in regulatory affairs to provide strategic guidance and oversight to in-market partners.Key ResponsibilitiesDevelop and...
-
Global Regulatory Affairs Specialist, Virology
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences Full timeJob DescriptionAt Gilead Sciences, we're dedicated to creating innovative therapies that improve lives worldwide. Our team of experts is passionate about tackling complex diseases, and we're seeking talented individuals to join our mission.Function:Global Therapeutic Area (TA) Regulatory Affairs, VirologyPosition Overview:As a Regional Regulatory Lead,...
-
Regulatory Affairs Director for Global Products
4 weeks ago
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeAbout the RoleGilead Sciences International, Ltd. is seeking an experienced Regulatory Affairs Director to lead the development and implementation of global regulatory strategies for our products.Key ResponsibilitiesDevelop and implement global regulatory strategies for multiple products in the post-marketing phase of development.Represent Gilead in...
-
Cambridge, Cambridgeshire, United Kingdom Gilead Sciences International, Ltd. Full timeKey Responsibilities:As a Director, Global Regulatory Affairs, Precision Medicine, you will develop and execute precision medicine regulatory strategies in alignment with the drug global regulatory strategy, collaborating with cross-functional stakeholders across the Gilead therapeutic areas and adhering to the appropriate regulations. You will work closely...