Beschreibung
Regulatory Manager with profound CMC knowledge wanted for our Basel based client in the pharmaceutical sector.Your experience/skills:
- Science based Bachelor's or Master's degree, higher degree, like MD, PhD or PharmD, preferred
- 2+ years' experience in regulatory and drug or biologic development spanning activities in Phases I-IV including a sense of post-marketing and brand optimisation strategies, commercial awareness is beneficial
- Familiarity with regulatory submission and approval processes in at least one major region
- Skill set consisting of social intelligence and abilities, negotiation expertise and solution finding proficiency
- Languages: fluent English both written and spoken, other languages advantageous
Your tasks:
- Implementing regulatory strategy and controlling operational activities for assigned regions
- Giving input on global regulatory strategy and contributing to Regulatory Functional Plan and Seed Document, or their equivalents, including classification of gaps or risks in global strategic plans for set regions
- In charge of submission of Clinical Trial Applications, CTAs, and Investigational New Drugs and INDs
- Managing, planning, and arranging submissions of dossiers in assigned regions at a global scale
- Securing regulatory compliance for assigned projects and maintaining records of all major Health Authority interactions in the validated document management system
Start:
Duration: 07MM+
Location: Basel, Switzerland
Ref.Nr.: BH13887
Does this sound like an interesting and challenging opportunity to you? Then take the next step by sending us your CV as a Word document and a contact telephone number.
Due to work permit restrictions we can unfortunately only consider applications from EU or Swiss citizens as well as current work-permit holders for Switzerland.
Going the extra mile…
New to Switzerland? In case of successful placement, we support you with:
- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more