Medical affairs jobs in Chalfont Saint Peter

Experience of working in medical affairs in the pharmaceutical industry * Therapeutic area experience of neurological disorders would be a plus * Possible experienced in vendor medical communication ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Serve as a local Medical Affairs representative in standing and project-based cross-functional teams * Provide medical and scientific expertise supporting cross-functional projects (e.g., materials ...

Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and ...

Leading Scientific Publications for journal and congress submissions, including publication planning and delivery Experience of working in medical affairs in the pharmaceutical industry Therapeutic ...

... Affairs initiatives. The role will provide technical/scientific consultation to both the Scientific and the commercial teams to ensure accuracy and compliance with the standard and local rules and ...

Are you in the Buckinghamshire area and seeking that next step in your career within Regulatory Affairs in the Medical Device industry? 🏥 You will spend majority of your time in the beautiful ...

Private Medical Insurance following completion of 3 months' service (this is a taxable benefit ... affairs of a wide-ranging portfolio of corporate and personal clients. You will develop technical ...

Zest Scientific is actively recruiting for a Senior Regulatory Specialist in the field of medical devices for a leading global drug development organization. We are seeking a motivated individual with substantial experience in Medical Device Regulation, particularly in the areas of combination pr...

Associate Director, Medical Affairs. If you're a strategic innovator within Medical Affairs, this is an opportunity for you. ...

Great mix of global and EU med affairs and commercial work, across an established and growing osteoporosis account. ...

CK Group are recruiting for a Regulatory Affairs Associate to join a biopharmaceutical company who are based in Uxbridge on a contract basis for 12 months. Regulatory Affairs Associate Role:. Experience in a Regulatory Affairs role in CMC, including preparation of submissions to Agencies and fami...

Extensive experience in Regulatory Affairs with experience acting as therapeutic area European Regulatory Affairs lead, defining and implement regulatory strategies and executional plans. Define and advise the GRT on regional considerations in developing creative regulatory strategy, lead develop...

The role will encompass a large percentage of medical affairs work, as well as some promotional (and no publications!) The ideal candidate will have a blend of creative, visual experience, as well as the knowledge and confidence to work across high science accounts/projects. ...

Expertise in authoring and reviewing of regulatory documents; development regulatory documents; Regulatory Strategy Plans, Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Orphan Drug and Paediatric plans/applicati...

Medical Scientific Advisor | Diabetes. We are working with a leading healthcare provider, as an exciting opportunity has arisen for a Scientific Advisor who will assist in the development of, and conduct a variety of Scientific Affairs initiatives. Develop and review training documents to check m...

Working with the regulatory team (and core stakeholders across multiple areas), your role will be to operate as a Regulatory Lead, providing centralised regulatory strategy and guidance across the region and make sure that regulatory deadlines and approvals are achieved. A global pharmaceutical c...

Regulatory Affairs Advisor (Arabic Speaking). At Campden BRI, we have a dedicated Regulatory Affairs Team who offer a valuable and expert advisory service, as we're the leading authority, helping our clients stay compliant with food regulations in more than 80 countries! We are widely recognised ...

Principal Medical Writer Opportunity. Join a dynamic and ambitious truly independent agency as a Principal Medical Writer and immerse yourself in diverse, exciting med affairs, meded and omnichannel projects. ...

If you would like an exploratory chat about this role or the other opportunities available, please get in touch via elaine@medicaltalent. ...

Medical Science Liaison – Nephrology / Rare Diseases. Providing medical information and responses to complex medical questions from clinicians. Working as part of a wider team, but with sole responsibility for specialist centres across UK, Netherlands and Ireland from a medical affairs standpoint...

Implements product related regulatory strategies, Regulatory Affairs processes and activity planning in accordance with national legislation and regulatory requirements. Partner with regional management and peers to ensure consistency in procedures and agency interactions Regulatory Research Main...

Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone regulatory project, with guidance from senior staff as appropriate. May write new regulatory SOPs and regulatory intelligence databanks, and/or propose r...

Associate Director Regulatory Affairs. Works with the Lead, Regulatory Affairs, and the Development Team, and with moderate/minimal supervision, with select project teams within subsidiary organizations to develop and oversee program-specific regulatory, clinical, and development strategies. Resp...