Candidates must meet the following requirements to be considered for this exciting opportunity:
* 10+ years of industry experience * Excellent communication skills; ability to explain methodology to non-statisticians * Ph.D. in Biostatistics or related field (M.S. may be considered) * Previous management experience, including direct reports * Preferably experience in vaccines, respiratory, inflammation, auto-immune
Calling German Speaking Regulatory Affairs Professionals!
Are you a regulatory affairs professional looking for their next career step within the medical device industry? Then we could have the ideal role for you. Specializing within regulatory affairs allows us to get you the best and hottest roles! We are currently looking for German speaking regulatory affairs professionals.
UK Medical Director â€“ Niche Pharma, UK.
Company:Network Jobs Location: United Kingdom, Not Specified, London Salary: 100,000+
Closing Date: 13 Dec 13
Our client requires a UK Medical Director to direct Medical Affairs, working closely with marketing, sales and parallel commercial functions. The incumbent will review and approve all advertising, sales and promotional activities, in addition to supporting Pharmacovigilance and Code training.
This position will report into the EU Medical Director, and be responsible for UK Medical Advisors, Medical Affairs Managers and Medial Information personnel. ...
Excellent opportunity with a growing global leader in the pharmaceutical industry. In this role you will make a significant impact on future European regulatory strategy of many products, both innovative and established. Given the current growth in the company and a very strong product pipeline you can realistically see yourself moving into international regulatory affairs at a senior director level within a few years.
Risk Manager-Growing Medical Device Company-Suisse
Take the first step towards this fantastic opportunity to be part of the growth of this medical device company in a great management role. Our client are looking for a risk manager to work within their regulatory affairs and quality assurance department and work on the risk assessment of our client's innovative medical devices. If you are experienced in the risk assessment of medical devices and are looking for a managerial role ensure you apply today!
This is an exceptional opportunity to represent a global Pharmaceutical company from one of their sites in Basel. The role of Trial Quality Manager requires an experienced Clinical Researcher (at least 8 years' with 6 years in oncology and at least 4 as a CRA or QA Auditor) to act as the central point between the clinical trial team and the field.
My client is a leading Medical Devices company, located north of Zurich. They are looking for a dedicated and experienced Quality Engineer who has worked in a GMP environment in Process, Test Method, Equipment and Design Validation.
My client are a leading Pharmaceutical company based in Surrey. They are hiring for a Regional Medical Head of Transplant. It is vital that candidates have a solid background in transplantation to apply for this role. For full details please contact Emma Hobbs firstname.lastname@example.org 01483 228 190
Medical Monitor, Hematology/oncology
Company:Real Staffing Location: Dublin Salary: 100,000+ Benefits: Depends on Experience
Closing Date: 01 Jan 14
* Extensive interaction with academic thought leaders to optimize clinical trial strategies and clinically manage the conduct of the clinical trials * Collaborate with Clinical Science and Medical Writing department in the preparation of clinical development plans, protocols, investigator brochures, annual IND reports, clinical study reports, manuscripts, and different scientific presentations * Work cross-functionally to define, plan and provide Medical ...
Quality Manager - Contract - North West, UK
Company:Real Staffing Location: North West England Salary: 100,000+
Closing Date: 31 Dec 13
* To ensure the QA activities of Products comply with the requirements of Medical Device Directive MDD 94/42/EEC as amended and relevant cGMP, ISO13485 and FDA 21CFR 820. * Writing, reviewing and approving SOPs (standard operating procedures) to ensure compliance with relevant Quality Management Systems. * Establish and maintain the Quality Policy and Quality Manual. * Review, where applicable Quality Technical agreements.
Associate Director Health Economics - Oncology/Renal
Our client is looking for a quality professional to manage the entire cGMP QA requirements for the commercial release of drug substances, intermediates, and in-process as well as finished products. This individual will need to support all quality system procedures including risk management, supplier evaluation, change controls, non-conformances, and other aspects of the system. ...
I am looking for a Senior and Junior regulatory engineer. This function is a critical part of all regulatory and quality processes as you would be the main linkpoint between many different departments; regulatory, R&D, labs, quality and operations.
Locality Clinical Lead GP required, near the Coast of East Sussex up t
Company:Network Jobs Location: United Kingdom, Not Specified, Sussex Salary: 100,000+ Benefits: Uup to Â£105k pro rota + bonus of up to Â£6k
Closing Date: 14 Dec 13
Are you seeking a salaried post in the lovely coast of East Sussex? Merco Medical is currently seeking a Locality Clinical Lead GP for a Practice on the Coast of East Sussex. Fulltime or part time would be considered.
â€¢Salary up to Â£105k pro rota + bonus of up to Â£6k â€¢Tailored CPD â€¢37. ...
Director Medical Affairs - Manage a strong division
Company:Network Jobs Location: United Kingdom, Not Specified, South East Salary: 100,000+ Benefits: Comprehensive package
Closing Date: 13 Dec 13
Would you like to lead a strong UK Medical Affairs division? In this position you will be responsible for the overall management of the medical affairs group in the UK and will play an instrumental role in the growth of the function in the UK. My client is a well established specialty pharmaceutical company who are very strong in their niche area and are now looking to build on this strength and expand into new markets. ...
Hydrogen Life Sciences has been requested to search and select a Head of e-Compliance (CSV). This permanent/staff position is required for a Global leader in pharmaceuticals based in Basel, Switzerland.
Senior Director Medical Affairs Oncology Global â‚¬140,000 to â‚¬200,000 Package Car, Bonus, Pension
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