The Client is a group of companies dedicated to researching, developing, manufacturing and marketing novel products of high therapeutic value for human and veterinary medicine. It is one of the world’s 20 leading pharmaceutical companies. Business Areas include: Prescription Medicines, Consumer Health Care, Industrial Customer, Biopharmaceuticals, Pharmaceuticals, Production, Pharma Chemicals, and Animal Health. Research & Development: The Company is spending 22% of net sales in their largest business segment Prescription Medicines (2008) on R&D. They have four main R&D sites and three smaller specialized sites worldwide, which focus on seven major therapeutic areas: Respiratory diseases, Cardiovascular diseases, Oncology, Central nervous system (CNS) diseases, Virology, Metabolic diseases and Immunology and Inflammation.
They are currently investing substantially in Oncology. Our client has a full pre-clinical and phase I-III pipeline. All compounds are from the client’s in-house research, and include small molecules and biologics.
This position will be responsible for one new PIII product for primary and secondary indications in a growing team of Medical Advisors. Primary function at this Corporate Medical Affairs appointment is to provide strategic input for global lifecycle management and medical expertise and strategic planning to allow for effective, scientific and medical global pre-launch and drug commercialization leadership.
Position Description:
Investigator Initiated Studies – experience in developing, conducting, contracting and interpretation of PI-III GCP studies as well as experience in networking
Opinion Leader Management Previous work with Oncology KOL’s; publication plan to meet strategic objectives for primary and secondary indications; experience organizing symposia, investigator meetings, board meetings and CME events
Close Co-operation with Marketing and link Marketing and Clinical Research (seen as a special challenge) – Materials and message development; input to primary and secondary publications and sales training materials
Scientific literature research, critical analysis and summarisation of product, disease state and competitor literature
Medical writing and revision of manuscripts - documents – dossiers, clinical overviews, expert opinions, PSURs, ASRs
Medical input to the marketing plan and publication plan.
Requirements:
University degree in Medicine is preferred with a preference for board certification in the TA; alternatively, a PhD with significant experience in a large country or regional role in oncology is required
Three to five years experience within the pharmaceutical industry, preferably in medical affairs, clinical research or medical marketing
Clinical experience or specialisation in Oncology or Hematology/Immunology
Ability to work effectively in an international, cross-functional environment
Competency to quickly grasp scientific principles and to develop expert understanding in the relevant field
Strong analytical thinking skills and capacity to identify trends in medical sciences
Experience in conducting Phase IIIb-IV trials including results analysis and publications strategies
Excellent oral and written English skills are essential with a desire to learn German well accepted
Experience in basic aspects of biostatistics and clinical trial design
As we would like to build up an international team, candidates with global background would be appreciated
An established track record in lung, ovarian or breast cancer would be of advantage.
How to apply for the Global HQ Medical Advisor; Oncology role:
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Send your completed job application through to us for processing.
Alternatively, for a confidential discussion concerning the Global HQ Medical Advisor; Oncology opportunity you can telephone Robert Bates on +49 (0) 69 219 776 0. Please be sure to quote 09870 in all correspondence relating to this role.
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