Company: Advanced Regulatory (EU Roles)
Reference: ADV SwissOption2
Closing Date: 22 May 13
Type: Full Time
Salary (ÂŁ): 40,000 - 60,000
Benefits: Excellent Salary - Including low tax and FULL RELOCATION
Forward thinking client which is rated in the Top 10 of world Pharmaceutical companies - Excellent Benefits package which includes a great salary & benefits package - Strong pipeline with Oncology, CNS, Pain, Inflammation and Cardiovascular products in late phases of development - Location: Switzerland, Basel, NeuchĂ˘tel, Geneva, In the first instance please call Matt or Theo on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com
Regulatory Affairs Project Manager / Full RA responsibility from development through to registration / Pick up fantastic career development Switzerland /
Does your expertise lie in Regulatory affairs project management? Do you want a fresh challenge with a forward thinking pharmaceutical company? Would you like to work in a strategic and enterprising role???
•Join a forward thinking client which is rated in the Top 10 of world Pharmaceutical companies.
•Receive excellent package which includes a great salary up to 160,000CHF.
•Work with a strong pipeline with Oncology, CNS, Pain, Inflammation and Cardiovascular products in late phases of development.
This company has an impressive development pipeline and an established portfolio of marketed products across its core therapeutic areas. My client is seeking a Senior Regulatory Project Manager experience to work in a broad based European project management role. This is a pivotal role in the design, development and implementation of European development and filing strategies.
Role / Description:
In the long term you will pick up fantastic development experience as this company is ready to break into new markets with new indications and new dosage forms planned for recently identified markets. So you will constantly be faced with new challenges and new opportunities to pick up and utilise new skills as you help to lead this amazing company into new horizons.
You will need to be a proactive, strongly self-motivated and achieving Regulatory Affairs professional working in the pharmaceutical industry with proven experience in successful project management and European product registration.
In the first instance please call Matt or Theo on +44(0)207 801 3384 or +44 (0) 7918 195 166 or please send a full CV to Theo@advregulatory.com
Benefits: FULL RELOCATION, strong package, very low tax and a bonus.
Keywords / Key words: Swiss Regulatory / Switzerland Regulatory / Regulatory Project Mabager / Regulatory Submissions / Regulatory Filings / Regulatory / Regulatory / Regulatory Affairs / Reg Affairs / Regulatory / Regulatory / Regulatory / Regulatory, Clinical Research, RA, Project Manager, Centralised, Submissions, Pharmaceutical, Biotechnology / Bio.
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