Medical Project Manager

Role Expectations

The Medical Project Manager will support the Medical Manager in overseeing and executing medical projects related to Cardiovascular and Metabolic Diseases (CMVD).

The role involves coordinating clinical trials, managing medical project (timelines, results) and ensuring compliance with regulatory requirements.

The ideal candidate will have a strong background in medical sciences, excellent project management skills, and the ability to work collaboratively with cross-functional teams.

Main Responsibilities

1. Project Coordination:
   - Assist the Medical Manager in planning, executing, and monitoring medical projects.
   - Coordinate clinical trials and ensure adherence to project timelines and budgets.
2. Data Management:
   - Collect, analyse, and interpret clinical data.
   - Prepare scientific documentation and reports.
3. Regulatory Compliance:
   - Ensure compliance with regulatory requirements and company policies.
   - Support pharmacovigilance activities and risk management strategies.
4. Stakeholder Communication:
   - Communicate project updates and findings to internal and external stakeholders.
   - Build and maintain relationships with healthcare professionals and regulatory authorities

Required Skills and Experience

1. Educational Background :
   • Bachelor’s degree of Doctor or Pharmacist required.
   • Advanced degree (e.g., Master's, PhD) in a relevant field such as Cardiology, Endocrinology, or Clinical Research is preferred.
2. Professional Experience:
   • Minimum of 1 year of experience in medical affairs, clinical research, or project management within the pharmaceutical industry.
   • Experience in Cardiovascular and Metabolic Diseases (CMVD) is highly desirable.
   • Proven experience in managing clinical trials and medical projects.
   • Familiarity with regulatory affairs and compliance standards
3. Medical and Scientific Knowledge:
   • Understanding of CMVD and related therapeutic areas.
   • Ability to interpret and analyze clinical data.
4. Technical Skills:
   • Competence in medical writing and scientific documentation.
   • Familiarity with medical databases and statistical software.
   • Competence in using medical and clinical trial management systems.
5. Regulatory and Compliance Knowledge:
   • Understanding of regulatory requirements for drug development and approval processes.
   • Knowledge of pharmacovigilance and risk management
6. Leadership Skills :
   • Autonomous
   • Collaborative mindset with a focus on teamwork and partnership.
7. Ethical and Professional Integrity:
   • Commitment to ethical practices and professional integrity.
   • Strong sense of responsibility and accountability.
8. Communication Skills:
   • Good verbal and written communication skills.
   • Ability to present complex medical information clearly and concisely.
9. Project Management Skills:
   • Strong organizational and project management abilities.
   • Proven experience in managing project timelines, budgets, and resources
10. Analytical Skills:
    • Strong analytical skills to evaluate clinical data and make informed decisions.
11. Interpersonal Skills:
    • Ability to build and maintain relationships with key stakeholders, including TAEs, HCPs

Whatever your area of expertise, your work within the Servier Group helps advance therapeutic progress for the benefit of patients. You will be part of teams recognized for their scientific excellence and reach your full potential in a professional environment that encourages you to develop yourself. Tailor-made onboarding journeys, mobility opportunities, quality trainings, responsible management, team spirit... All this and more in a workplace focused on your well-being.

At Servier, we are committed to therapeutic progress to serve patient needs. We put the diversity of our employees as a source of richness for the fulfillment of this vocation.