I am recruiting for a Senior Clinical Programme Lead to focus on the therapeutic area of oncology and haematology. This one of my client's main indications, and they have a well-established research dedicated solely to oncology. As a result, it is an area that the company has really invested, meaning that it is extremely well-funded. Due to this, the role comes with a lot of long term scope, leading to an interesting and career path full of potential.
Do you have sound experience with class III medical devices? And a technical/medical/scientific degree? In addition, solid knowledge of EU regulations as well as other countries' regulations? On top of this, you speak fluent German and English? And nonetheless, you have quality management experience? Then you have the right profile for the Vigilance & Post Market Surveillance Manager position within a growing and succesfull company.
A major biotechnology company based in Switzerland working in the field of drug therapy for inflammatory disorders. The company operates in more than 50 countries worldwide, distributing to major medical centres that use its advanced compounds in over 200 trials.
IT Business Analyst â€“ 2 year contract â€“ Global Pharma - Â£500 per day
The Hydrogen Group has been appointed to search and select a Senior Manager, Global Regulatory Project Leader on behalf of a large global pharmaceutical company that is present in more than 150 Countries in the world. The company has a growing portfolio of Innovative products in key therapeutic areas. They are currently looking for an experienced Regulatory Affairs professional to join their Global Regulatory Affairs team.
QP Head Of Quality - High Living Standards - Switzerland
A global pharmaceutical company located in Switzerland, a country known for its beautiful sites and high living standards, is looking for a Head of Quality Swiss QP to join their team in Switzerland. My client has invested in their consumer care division and seeks for talented individuals to help it grow.
* Manages overall operation of the entire clinical study including project planning, budget, resource management and CRO management * Directs the design, documentation, testing and implementation of clinical data collection studies, external reproducibility studies and clinical database review * Ensures GCP ICP regulatory compliance * Develop and manage clinical budget and contingency plans for clinical trials * Manage full scope of stud ...
My client, a large international pharmaceutical company is looking for an experienced Distribution Manager to join their growing team. ...
Director of Risk and Safety Management - Germany wide (home based)
Company:Meet Location: Germany home based Salary: 100,000+ Benefits: â‚¬120,000 - â‚¬130,000 + excellent benefits - email firstname.lastname@example.org
Closing Date: 10 Apr 14
Director of Safety and Risk Management â€“ Germany, Home or office based â€“ up to 120,000 Euros + bonus. Position suitable for Pharmacovigilance Director, Senior Physician, Clinical Safety Director, Risk and Safety Director, PV Business Development Specialist â€“ preferably with CRO experience. This role is open to candidates with all therapeutic backgrounds. Please email email@example.com with a copy of your CV.
Medical Director, Medical Affairs - Nephrology (US - West Coast)
This role will interface with many internal and external stakeholders, including the medical science liaison (MSL) team, commercial personnel, R&D personnel, senior management, research institutions, and outside medical experts.
A new position has arisen within my client due to continued growth of the company, particularly the Swiss operations. You will be working alongside the quality assurance (QP) team focusing on release and distribution of products to the Swiss market. My client focuses on allergy products and is going through a period of sustained growth.
I am working on behalf of a vastly expanding and dynamic Health Sciences firm who, based on a year of fantastic growth, are looking for a pragmatic market access professional to join and lead their European function in the capacity of European Market Access Director. The company has offices based across Europe, The US and Asia, and with this role in particular being based out of their London HQ.
Our client is a currently recruiting for an MD, Pharmaceutical Physician, with solid expertise in developing and running studies in the Haematology area. This is a full time, permanent position with an exciting pharmaceutical company based in the Zurich region.
Senior Director / Vice President - CNS/Neuroscience - US
A renowned company in the pharmaceutical industry is seeking a suitable individual to join them, to help lead their CNS/Neuroscience team based in the US.
Medical Director - Germany
Company:RBW Consulting Location: Germany Salary: 100,000+ Benefits: Full Beneift package
Closing Date: 07 Apr 14
This is an opportunity for a Medical Director who has an interest in Start Up companies and an interest/experience in Orphan Diseases.
There is a strong work from home component, with offices based in Frankfurt. Key elements of the role is sound knowledge of the German market and requirements and an ability to contribute to the management team of this Affliate.
A part-time position within regulatory affairs has come in for an experienced regulatory affairs professional within the medical device industry. This is a great role which provides excellent flexibility options and the option to work partly from home. The role is with a leading company that specialise in the dental industry. If you are an experienced regulatory affairs professional within the medical device industry who speaks fluent German we want to hear from you today!
This company pride themselves on their professional approach and their close relationship with customers across Switzerland. With their international HQ based in Switzerland, they are highly specialised in the field of orthopaedics and this is your chance to join them as a Sales Specialist, selling and promoting their spinal product portfolio across the North East of Switzerland (Zurich, Winterthur, St. Gallen etc.).
Regulatory Affairs Specialist-Develop your career-Devices-CH
Take the first step towards developing your regulatory affairs career today, by applying to this fantastic regulatory affairs specialist role! Our client are looking for a regulatory affairs professional who has several years of experience within medical devices. The senior management that you will report into within this role are looking for someone that they can develop and train into management, providing you with fantastic future opportunities to develop into management!
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