Medical Affairs
5 - 12 Years of ExperienceNot disclosed Full Time
Bharat Biotech Pvt. Ltd.
Hyderabad, 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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