Medical Director

Get AI-powered advice on this job and more exclusive features.Direct message the job poster from Meet Life SciencesClinical Development Expert | Associate Recruiter at MeetFreelance Medical Director – Pharmaceuticals | 12-Month Contract | SwitzerlandWe 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 . If you are an experienced Medical Director ready for an exciting challenge, I’d love to discuss this opportunity with you!Seniority levelDirectorEmployment typeContractJob functionScienceIndustriesBiotechnology Research and Pharmaceutical Manufacturing#J-18808-Ljbffr