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- Aufgaben: Lead medical strategy for clinical development and oversee trials in a dynamic pharmaceutical environment.
- Arbeitgeber: Join a trusted partner in the pharmaceuticals industry, focused on innovative medical strategies.
- Mitarbeitervorteile: Freelance contract with the chance to work on cutting-edge projects in Switzerland.
- Warum dieser Job: Make a real impact in clinical development while mentoring a team of medical professionals.
- Gewünschte Qualifikationen: MD with 10+ years in clinical development; strong in medical strategy and regulatory guidelines.
- Andere Informationen: Exciting opportunity for experienced Medical Directors looking for a challenge!
Das voraussichtliche Gehalt liegt zwischen 120000 - 168000 € pro Jahr.
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Direct message the job poster from Meet Life Sciences
Clinical Development Expert | Associate Recruiter at Meet
Freelance 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 . If you are an experienced Medical Director ready for an exciting challenge, I’d love to discuss this opportunity with you!
Seniority level
- Director
Employment type
- Contract
Job function
- Science
- Industries
- Biotechnology Research and Pharmaceutical Manufacturing
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Medical Director Arbeitgeber: Meet
Kontaktperson:
Meet HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Medical Director
✨Tip Number 1
Make sure to leverage your network in the pharmaceutical industry. Reach out to former colleagues or connections who may have insights into the company or the hiring manager. A personal referral can significantly boost your chances of landing an interview.
✨Tip Number 2
Stay updated on the latest trends and developments in clinical research and regulatory guidelines. Being knowledgeable about current practices will not only help you in interviews but also demonstrate your commitment to the field.
✨Tip Number 3
Prepare to discuss specific examples from your past experience that showcase your leadership in clinical trials and medical strategy. Highlighting your ability to manage cross-functional teams and navigate complex projects will set you apart.
✨Tip Number 4
Familiarize yourself with the company's recent projects and initiatives. Showing that you understand their business objectives and how you can contribute to them will make a strong impression during your discussions.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Medical Director
Tipps für deine Bewerbung 🫡
Tailor Your CV: Make sure your CV highlights your 10+ years of experience in clinical development, particularly within the pharmaceutical or biotech industry. Emphasize your expertise in medical strategy and clinical trial design.
Craft a Compelling Cover Letter: Write a cover letter that showcases your leadership skills and ability to manage cross-functional teams. Mention specific examples of how you've contributed to clinical development projects and regulatory submissions.
Highlight Relevant Skills: In your application, clearly outline your knowledge of GxP and Good Clinical Practice (GCP). Include any experience you have with regulatory filings and interactions with health authorities.
Showcase Communication Skills: Since excellent communication is key for this role, provide examples of how you've effectively presented complex medical data. This could be through previous presentations, reports, or publications.
Wie du dich auf ein Vorstellungsgespräch bei Meet vorbereitest
✨Showcase Your Medical Expertise
Be prepared to discuss your extensive experience in clinical development and how it aligns with the responsibilities of the Medical Director role. Highlight specific projects where you led medical strategies or oversaw clinical trials.
✨Demonstrate Leadership Skills
Since this role involves mentoring and leading a team, share examples of how you've successfully managed cross-functional teams in the past. Emphasize your ability to drive project progress and ensure effective performance.
✨Understand Regulatory Compliance
Familiarize yourself with GxP and Good Clinical Practice standards, as well as regulatory guidelines relevant to the pharmaceutical industry. Be ready to discuss how you've ensured compliance in previous roles.
✨Communicate Clearly and Effectively
Prepare to present complex medical data in a clear and concise manner. Practice explaining your clinical trial designs and outcomes, as strong communication skills are crucial for this position.
