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Title
Text copied to clipboard!Medical Science Manager
Description
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We are looking for a highly skilled Medical Science Manager to lead and coordinate medical research and clinical development initiatives within our organization. The ideal candidate will have a strong background in medical science, excellent leadership abilities, and the capability to manage cross-functional teams to ensure the successful execution of clinical trials and scientific projects. This role involves close collaboration with research scientists, clinical teams, regulatory affairs, and marketing departments to translate scientific data into actionable insights that support product development and commercialization strategies. The Medical Science Manager will also be responsible for maintaining up-to-date knowledge of medical and scientific advancements, ensuring compliance with regulatory standards, and effectively communicating complex scientific information to both internal stakeholders and external partners. This position requires a proactive approach to problem-solving, strategic thinking, and the ability to manage multiple projects simultaneously in a fast-paced environment.
Responsibilities
Text copied to clipboard!- Lead and oversee clinical research projects and medical studies.
- Collaborate with cross-functional teams including R&D, regulatory, and marketing.
- Develop and implement medical strategies aligned with organizational goals.
- Ensure compliance with regulatory requirements and ethical standards.
- Analyze and interpret clinical data to support product development.
- Prepare scientific documents, reports, and presentations for stakeholders.
- Manage relationships with key opinion leaders and external partners.
- Provide medical expertise and training to internal teams.
- Monitor scientific literature and industry trends to inform strategy.
- Support regulatory submissions and interactions with health authorities.
Requirements
Text copied to clipboard!- Advanced degree in medical science, pharmacy, or related field (PhD, MD preferred).
- Proven experience in clinical research and medical affairs.
- Strong knowledge of regulatory guidelines and clinical trial processes.
- Excellent communication and leadership skills.
- Ability to analyze complex scientific data and present findings clearly.
- Experience managing cross-functional teams and projects.
- Familiarity with therapeutic areas relevant to the company’s portfolio.
- Proficiency in medical writing and scientific documentation.
- Strong organizational and multitasking abilities.
- Willingness to travel as required.
Potential interview questions
Text copied to clipboard!- Can you describe your experience managing clinical research projects?
- How do you stay updated with the latest medical and scientific developments?
- Describe a time when you had to communicate complex scientific information to a non-expert audience.
- What strategies do you use to ensure compliance with regulatory standards?
- How do you manage collaboration between different departments?
- Can you provide an example of a successful medical strategy you developed?
- How do you handle conflicts within cross-functional teams?
- What experience do you have with regulatory submissions?
