Medical Affairs

Medical Affairs

work outline icon5 - 12 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Bharat Biotech Pvt. Ltd.

time outline iconHyderabad, Telangana, India

Posted on 15-09-2023

793 Views

1 Vacancy

Description

  • Ensuring that all output complies with the European Medicines Evaluation Agency (EMEA) regulations, Dutch codes of practice and license conditions where necessary.
  • Overseeing medical premarket approval of new chemical entities (NCEs).
  • Identifying study-related regulatory and quality issues, and managing complaints and any subsequent legal actions.
  • Designing and implementing campaigns such as those for disease awareness and medical education, depending on the organisation’s products.
  • Participating in meetings with senior management and attending external meetings and congresses on behalf of the company.
  • Developing the best possible working relationships between the organisation and stakeholders, especially key opinion leaders.

Category

Pharmaceuticals

Functional Area

Regulatory Affairs / Pharmacovigilance

Key Skills

Communication SkillsProblem Solving SkillsDecision MakingEmpathyTeam Work

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