Leadership opportunity in Global Clinical Development
Clinical Research Manager - Frankfurt area - 12+ months (m/w)
Company:Amoria Bond Location: Frankfurt am Main Salary: 100,000+
Closing Date: 08 Aug 16
Clinical Research Manager - Frankfurt area - 12+ months (m/w)Amoria Bond is currently looking to hire a Clinical Research Manager for one of our clients within the pharmaceutical industry for a maternity leave replacement. The company focuses on research and development in the area of oncology drugs. The initial contract is scheduled for 12 months with a high chance of being extended by another 6 months, depending on study quality and collaboration. ...
Regulatory Program Manager, Basel, 12 month contract
My client, a blue chip top 5 pharma based in Basel, is currently seeking an experienced Regulatory Program Manager to join their team on a 12 month contract basis. Within this role you will be responsible for EU & ROW regulatory strategy and operational management of a project.
Drug Safety / Pharmacovigilance (PV) Safety Data Exchange Agreements Expert (SDEA) Level: Mid Level Salary: Negotiable depending on experience Contract type: PermanentThe Hydrogen Group is looking for an exceptional candidate to join their Global client as a Drug Safety SDEA expert. This multi-national client is looking for someone with a strong background in managing, drafting and reviewing SDEAs between multinational companies. ...
Senior Product Manager, Medical Marketing
Company:EPM Scientific Location: New Jersey Salary: 100,000+ Benefits: bonus
Closing Date: 05 Aug 16
Senior Product Manager, Medical Marketing | Pharmaceuticals | Pain Management$150,000 - $170,000New Jersey, USAA rapidly expanding, global pharmaceutical company is looking to hire a Senior...
QA Validation Specialist (6 Month Contract) – Basel – 100CHF P/HRI am currently looking for someone to take an urgent contract within a medical devices company in Switzerland. This position is based within the QA team of a successful company who are looking for a validation specialist to begin working very soon.Tasks * Supporting the Process Validation projects, making sure that activities are compliant with QMS and external guidelines (FDA & EU). * Facilitate risk assessment/FMEA process. ...
Cleaning Validation Engineer – Frankfurt – 6m – up to €80phr
Cleaning Validation Engineer – Frankfurt – 6 Months’ – up to €80 per hour.My Client is currently looking for a Cleaning Validation Engineer with experience in Change Controls using Sentry System. Experience with single use equipment would be beneficial to your application. This role will be 60% revolved around the change controls and 40% on cleaning validation, my client would like someone with hands on experience developing a new cleaning cycle. ...
Senior Pharmacovigilance and Drug Safety Physician
Pharmacovigilance (PV) Physician - Switzerland Basel Level: Pharmacovigilance (PV) Physician Salary: Negotiable Duration: 12 months + ExtensionsThe Hydrogen Group is looking for an exceptional candidate to join their Global client as a Global Drug Safety Physician. This multi-national client is looking for someone with a strong medical background managing large and complex portfolios. ...
The Hydrogen Group has been appointed to search and select a Director, Regulatory Affairs, Biosimilars to join one of the fastest growing Biosimilars Units in the industry at present. This is a key strategic and leadership position within a large biopharmaceutical organisation with a fantastic legacy of development and innovation.Please contact Nikolay Dimitrov on +44 (0)20 7002 0120 or email: firstname.lastname@example.org
Are you a CSV Specialist looking for your next step? Look here!Looking for the next job as a CSV specialist? Want to work for a company that is a leader in their market with great focus on their employees? If you speak German, keep on reading! My client is looking for a CSV specialist who also has good understanding about GXP to start as soon as possible. ...
Exclusive opportunity with one of the biggest Pharmaceutical Companies Globally - Promising Pipeline - Switzerland - Market Access - Health Economics - Evidence Generation - Clinical Trials - R&D - HEOR - Director - Lead - Senior Position -
Head of International Promotional Regulatory Affairs
I am currently searching for a Director of Global Regulatory Affairs and International Advertising and Promotional Materials to join a fast growing Pharmaceutical company based in Oxford on 6 month contract basis. Within this role you will be responsible for European (EFPIA) and International (ex-US) regulations governing the promotion of prescription pharmaceutical products.
Initially a 6 month project in Basel, this major pharmaceutical organisation is actively looking to hire a talented addition to their experienced SAS programming team. Very competitive rate please contact me directly to discus this.In summary, the senior programmer will be responsible for programming analysis datasets, pooled datasets, listings, and figures for oncology clinical trials and submission activities.
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