Global Clinical Affairs Manager
3 weeks ago
**About ARC Regulatory**
At ARC Regulatory, we are committed to expediting access to precision medicine clinical trials for patients globally. Our team of experts provides compliance excellence for companies in the precision medicine sector, supporting many of the world's leading pharmaceutical R&D companies in implementing unapproved diagnostics in their clinical development programmes.
We are seeking a highly skilled and experienced Global Clinical Affairs Manager to join our team. As a Global Clinical Affairs Manager, you will be responsible for the development and delivery of global clinical compliance solutions to client companies, ensuring that client objectives are met and exceeded at all times.
The ideal candidate will have a strong background in biological sciences or a related scientific subject, with a minimum of 3+ years of experience in IVD medical device clinical affairs/R&D. The successful candidate will also have demonstrable awareness of the requirements of clinical performance studies in accordance with the EU IVDR, as well as relevant regulations (e.g., ISO 20916, 21 CFR).
We offer a competitive salary of **£50,000 - £70,000 per annum**, depending on experience, plus free car parking, private health insurance, and other benefits. If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply.
Key Responsibilities:
- Develop and implement global clinical compliance strategies for client companies.
- Lead cross-functional teams to ensure timely and effective delivery of clinical compliance solutions.
- Provide expert advice on clinical research regulatory requirements and guidelines.
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