Reference: PW 6607
Closing Date: 14 Nov 16
Salary (£): Competitive
Benefits: Competitive salary and bonus scheme, car allowance, health, life cover, pension
A leader in biotechnology since 1980, our client was one of the first companies to realise the new science’s promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. The company has changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, bone disease, and other serious illnesses.
The company continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness
Key responsibilities will include:
Work with Local and global study management to ensure preparation, implementation and completion of studies
Work with health economics and Corp. Affairs Depts to ensure market access of products, engaging key stakeholders and payers, and contributing in value dossiers and other access/HE documentation
Develop study protocols and data analysis plans for Local studies; supports and executes Local study protocol preparation, filing, review and approval in line with company processes and policies
Participate in the development of International strategies and tactics in close collaboration with the international team.
Visit selected opinion leaders and study groups for strategic discussions and protocol development
Review Local/Sub-Regional ISS proposals prior to approval
Partner with the Product Manager in the development and execution of the Local/Sub-Regional product(s) lifecycle management plan
Provides input into site selection for studies
Oversee in-sourced/outsourced Medical programs and logistics
Support Local/Sub-Regional regulatory and ethics approvals for development protocols
Participate in/conduct Local /Sub-Regional Advisory Board Meetings, Investigator Meetings and/or Expert Panels
Provide Medical expertise for pipeline products
Provide Medical expertise for Health Economy and reimbursement requests
Member of the Local/Sub- Regional Product Teams
Deliver TA and/or product specific Medical training
Deliver medical expertise for review of promotional and non promotional materials
QUALIFICATIONS / EXPERIENCE REQUIRED:
You will be a fully GMC registered medical graduate with clinical experience in oncology or a closely aligned areas such as Immunology. You will be able to demonstrate clear career development within the pharmaceutical industry within Medical Affairs and be a certified ABPI signatory. Excellent candidates with good medical affairs experience in an aligned therapy area seeking a move into oncology will be considered.
For a confidential discussion please telephone Jonathan Elliott at AXESS Limited on 020 8560 2300. To apply, please click the "Apply for Job" button quoting reference PW-6607
Only candidates with EU work authorisation will be considered.
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AXESS has been operating since 1990
We are a recruitment business dedicated to the pharmaceutical industry, specialising in Medical Affairs, Regulatory Affairs & Clinical Development
We match professional candidates to the best permanent, contract and interim roles in the market
Visit us at www.axess.co.uk
12 Union Court,
Richmond upon Thames,
|Tel:||+44 (0)20 8560 2300|
|Fax:||+44 (0)20 8560 2033|
|Website:||Visit Our Web Site|
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