Regulatory Affairs Manager

Global Program Regulatory Manager with profound knowledge in Clinical Trial Applications (CTA) wanted for our Basel based client in the pharmaceutical industry.

YOUR EXPERIENCE/SKILLS:

- Relevant science based university degree
- 2+ years' working experience in the field of regulatory management
- Profound project management knowledge with proven ability to manage several projects and competing priorities
- Expertise in regulatory operations as well as planning and compilation of CTAs with special focus on European submissions
- Languages: fluent English both written and spoken

YOUR TASKS:

- Supporting the team in planning and tracking meetings and deliverables to support regulatory submissions
- Assisting regulatory lead in the preparation and submission of global original Clinical Trial Applications (CTA)
- Maintaining regulatory submission packages such as substantial amendments, DSURs and Investigator Brochures
- Evaluating regulatory implication of non-clinical and clinical data as well as providing strategic regulatory input into selected clinical trials documents

START: ASAP
DURATION: 6MM+
LOCATION: Basel, Switzerland
REF.NR.: BH12424

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.

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In case of successful placement, we support you with:

- All administrative questions
- Finding an apartment
- Health - and social insurance
- Work permit and much more