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Title
Text copied to clipboard!Director of Medical Affairs
Description
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We are looking for a highly experienced and strategic Director of Medical Affairs to lead our medical and clinical development initiatives. This role is critical in bridging the gap between clinical research, regulatory affairs, and commercial teams to ensure the safe and effective use of our products. The Director of Medical Affairs will be responsible for developing and executing medical strategies, overseeing clinical trials, and providing scientific and medical guidance across the organization.
The ideal candidate will have a strong background in medicine or life sciences, with significant experience in the pharmaceutical, biotechnology, or healthcare industry. They will be adept at interpreting clinical data, managing cross-functional teams, and engaging with key opinion leaders (KOLs) and regulatory bodies. This role requires excellent communication skills, strategic thinking, and a deep understanding of the therapeutic landscape.
Key responsibilities include leading the development of medical education programs, supporting product launches with scientific data, and ensuring compliance with all regulatory and ethical standards. The Director of Medical Affairs will also play a pivotal role in shaping the company’s research agenda and contributing to the development of clinical protocols and publications.
This position offers the opportunity to work in a dynamic and innovative environment, where your expertise will directly impact patient outcomes and the success of our medical products. If you are passionate about advancing healthcare through science and collaboration, we invite you to apply for this leadership role.
Responsibilities
Text copied to clipboard!- Develop and implement medical strategies aligned with corporate goals
- Lead and manage clinical development programs and trials
- Collaborate with regulatory, commercial, and R&D teams
- Engage with key opinion leaders and external stakeholders
- Ensure compliance with regulatory and ethical standards
- Support product launches with scientific and clinical data
- Oversee the development of medical education and training materials
- Review and approve promotional and scientific content
- Contribute to the development of clinical protocols and publications
- Monitor and analyze clinical data to inform decision-making
Requirements
Text copied to clipboard!- MD, PharmD, or PhD in a relevant scientific field
- Minimum of 8 years of experience in medical affairs or clinical development
- Strong knowledge of regulatory requirements and clinical trial processes
- Excellent communication and leadership skills
- Proven ability to work cross-functionally in a matrix environment
- Experience engaging with KOLs and external stakeholders
- Ability to interpret and present complex scientific data
- Strong strategic thinking and problem-solving abilities
- Experience in a therapeutic area relevant to the company’s portfolio
- Willingness to travel as needed
Potential interview questions
Text copied to clipboard!- What is your experience in leading medical affairs teams?
- Can you describe a successful product launch you supported?
- How do you ensure compliance with regulatory standards?
- What therapeutic areas have you worked in?
- How do you engage with key opinion leaders?
- Describe your experience with clinical trial oversight.
- What strategies have you used to align medical and commercial goals?
- How do you stay current with medical and scientific developments?
- What role have you played in developing clinical protocols?
- How do you handle cross-functional collaboration challenges?
