Medical Director
vor 3 Wochen
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Clinical Development Expert | Associate Recruiter at MeetFreelance Medical Director – Pharmaceuticals | 12-Month Contract | Switzerland
We are looking for an experienced Medical Director for one of our trusted business partners operating in the pharmaceuticals industry. This is a freelance, 12-month contract based in Switzerland, offering the opportunity to work on cutting-edge clinical development projects and contribute to innovative medical strategies in a dynamic environment.
Key Responsibilities:
- Lead the medical and scientific strategy for clinical development programs and ensure alignment with business objectives.
- Provide medical oversight for clinical trials, ensuring regulatory compliance and high scientific standards.
- Collaborate with cross-functional teams including regulatory, safety, and clinical operations to drive project progress.
- Support the preparation and submission of regulatory filings and act as the primary point of contact for health authorities.
- Lead the design, execution, and interpretation of clinical trial data to ensure the successful delivery of clinical development plans.
- Oversee the medical review of clinical documents, including protocols, investigator brochures, and clinical study reports.
- Provide expert input into product development strategy and make recommendations for clinical programs.
- Mentor and lead a team of medical professionals, ensuring effective performance and development.
- Ensure that clinical trials meet GxP and Good Clinical Practice standards.
Skills:
- MD (Doctor of Medicine) qualification with 10+ years of experience in clinical development, preferably within the pharmaceutical or biotech industry.
- Strong experience in medical strategy, clinical trial design, and regulatory guidelines.
- Expertise in clinical data analysis and interpretation, with a deep understanding of clinical research methodologies.
- Proven ability to manage and lead cross-functional teams effectively.
- In-depth knowledge of GxP, Good Clinical Practice (GCP), and other regulatory requirements.
- Excellent communication skills, both written and verbal, with the ability to present complex medical data in a clear and concise manner.
- Experience in regulatory submissions and interactions with health authorities.
- Ability to work independently and take ownership of complex projects with a high degree of responsibility.
Apply Now
Please contact me directly with your updated CV and send it to my email at esra.diblan@meetlifesciences.com. If you are an experienced Medical Director ready for an exciting challenge, I'd love to discuss this opportunity with you
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