Regulatory Affairs Specialist for EU Oncology Portfolio

Your new companyGlobal Biotechnology in the UK is looking for a Regulatory Affairs Senior Manager to develop and implement regulatory strategies for EU markets for their Oncology portfolio in development. This position will sit within the global regulatory team and will require someone to have both development and post-marketing experience.Your new roleAs a...

Senior Regulatory Affairs Associate / Regulatory Affairs Manager EU contract jobYour new company This global biopharmaceutical company is looking for an experienced Regulatory Affairs professional to join them on a contract basis, 12 month, hybrid contract job with scope for extensionYour new role As Senior Regulatory Affair Associate / Regulatory Affairs...

Senior Regulatory Affairs Manager - CMCLifelancer is seeking a highly experienced Senior Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will be responsible for ensuring compliance with regulatory requirements and guidelines.This is a challenging role that offers the opportunity to work on diverse...

Park Street People Ltd is seeking a highly skilled Regulatory Affairs Manager to join their team on a 12-month temporary contract. The ideal candidate will have experience in CTA, EU, and early-stage development, as well as strong communication and interpersonal skills.The successful candidate will provide regulatory strategy and guidance across the region,...

Global Regulatory Affairs Manager - contract jobYour new companyThis well-known biotech is looking for an experienced Regulatory Affairs Manager to join their established Global Regulatory Affairs team. This is a 12-month contract job with scope for extension.Your new roleAs Global Regulatory Affairs Manager you will support the creation of strategy and...

Your new company A multinational pharmaceutical company is looking for a Regulatory Contractor on a portfolio basis to support them with their busy portfolio for EU markets.Your new role You will be part of the team that manages the procedural and operational aspects of the EU regulatory fillings with the EU CP, working in close collaboration with the EU...

An innovative global pharmaceutical company is currently looking for a Regulatory Affairs Manager with CTA, EU and early stage development experience to join their team on a 12 month temporary contract. Working with the regulatory team (and core stakeholders across multiple areas), your role will be to provide regulatory strategy and guidance across the...

Global Regulatory Affairs Manager - contract jobYour new company This well-known biotech is looking for an experienced Regulatory Affairs Manager to join their established Global Regulatory Affairs team. This is a 12-month contract job with scope for extension. Your new role As Global Regulatory Affairs Manager you will support the creation of strategy...

Global Regulatory Affairs Manager - contract jobYour new companyThis well-known biotech is looking for an experienced Regulatory Affairs Manager to join their established Global Regulatory Affairs team. This is a 12-month contract job with scope for extension.Your new roleAs Global Regulatory Affairs Manager you will support the creation of strategy and...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Specialist to join our team in Cambridge or Uxbridge. The successful candidate will play a critical role in supporting the regulatory team and contributing to our mission to serve patients.In this challenging position, you will be responsible for implementing the regional regulatory strategy...

Proclinical are recruiting for a Senior Regulatory Consultant - Oncology to join a pharmaceutical organisation. This role is on a contract basis with the ability to work remotely from anywhere in the UK. **Responsibilities**: - Guide the development of regional regulatory documents and meetings rendering to GRT methods. - Cooperation share regulatory...

Job DescriptionCMC Regulatory Affairs SpecialistWe are seeking a highly skilled CMC Regulatory Affairs Specialist to join our team at Regeneron Pharmaceuticals Inc.Key ResponsibilitiesRegulatory Submission ReviewReview regulatory submissions to ensure compliance with global regulations and CMC requirements.Collaboration and CommunicationCollaborate with...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a global biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a Senior Manager, Regulatory Portfolio Manager to join our team.Job SummaryThe Senior Manager, Regulatory Portfolio Manager will partner with Regulatory Leads and the Global...

Principal Regulatory Affairs Consultant - CMC small moleculeParexel, a leading Clinical Research Organization (CRO), is seeking a highly qualified Principal Regulatory Affairs Consultant (Associate Director level) with expertise in Chemistry, Manufacturing, and Controls (CMC) for small molecule. The ideal candidate will possess strong regulatory affairs...

We are seeking a talented Regulatory Affairs Specialist to join our dynamic team at BTA. As the CMC Regulatory Manager, you will play a vital role in our company's worldwide post-approval regulatory activities, specifically focused on Chemistry, Manufacturing, and Controls (CMC) for biological products.Key Responsibilities:Develop submission strategies and...

Transforming Patients' Lives through ScienceBristol Myers Squibb is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. As a Regulatory Affairs Specialist, you will play an integral role in work that goes far beyond...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a leading biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled and experienced Global Regulatory Lead to join our Oncology Drug Development team.Key ResponsibilitiesDevelop and implement global regulatory strategies for Oncology...

You will be part of a regional team dedicated to supporting the Regulatory Affairs function in the context of drug development particularly around procedures in place for the conduct of clinical studies through to the approval of a new drug. You will work both internally with colleagues and stakeholders in Regeneron. **Responsibilities include**: Work with...

Job Summary: We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Regeneron. As a key member of our regulatory team, you will be responsible for ensuring the compliance of our products with global regulatory requirements.Key Responsibilities:Review and assess regulatory submissions to ensure compliance with global regulatory...

Regulatory Affairs Senior Associate RoleWe are seeking a highly skilled Regulatory Affairs Senior Associate to join our team at Regeneron Pharmaceuticals Inc.About the RoleThis is an exciting opportunity for a talented individual with a passion for regulatory affairs to support our CMC Regulatory submissions. As a key member of our team, you will play a...