Project Manager Pharma Regulatory Authoring

PROJECT MANAGER PHARMA REGULATORY AUTHORING

On behalf of our client, a leading global pharmaceutical company, we are looking for a PROJECT MANAGER WITH PREVIOUS EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY (MANDATORY) AND WITH PHARMACEUTICAL REGULATORY AUTHORING. For this one year contract position based in Basel in Switzerland, our client is looking for an English speaking candidate who can start ASAP.

Are you looking for an exciting new opportunity with a market leading pharmaceutical company?

Then please have a look at the details:

THE SKILLS AND EXPERIENCE NEEDED FOR THIS ROLE ARE:

- Strong experience in IT Project Management (over 5 years experience)
- Experience in pharmaceutical regulatory authoring, publishing and submission tracking/planning mandatory
- Experience in working in global projects with multinational and virtual teams
- PMP or Prince2 certification
- Very good communication and stakeholder management skills
- Previous experience in the pharmaceutical industry is a must
- Willingness to travel
- Flexibility to work part time (80-100%)
- Excellent communication skills in English, other languages an advantage

If you are an energetic and highly motivated individual currently looking for an opportunity to apply your skills in a dynamic and challenging environment, then we look forward to receiving your application!

Apply today to secure your chance in this interesting opportunity for a Swiss globally well-known pharmaceutical company.

Please send your CV in English to Ms. Elodie Hanser. If you should have any questions, please do not hesitate to call her. Please only apply if you have an EU or Swiss nationality or if you already have an eligible work permit to work in Switzerland.

Probably you know Experis as Elan IT - we have a new name now but we still have the same expertise in IT Recruitment. We are part of the Manpower group and at Experis IT we are responsible for recruitment of the best IT Specialists.