Location: South East M3 / M4 / M40 Corridor
Reference: PW 6727
Closing Date: 24 Nov 16
Salary (£): Competitive
Benefits: Car / Bonus / Pension / Medical / Subsidised Restaurant
Blue-chip Global Pharmaceutical Company
Based West of London in the M3 – M40 Corridor
Flexibility to work from both home and the office
Development opportunity to final signatory
Develop and maintain in depth knowledge for assigned product(s) / relevant therapeutic area(s) through attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and by regular self-study of the national/international literature.
Provide expert medical/scientific advice for assigned Biosimilar products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to the development and medical and scientific accuracy of core dossiers generated by the medical department (i.e. pricing and reimbursement dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.).
Establish and maintain professional and credible relationships with key thought leaders / external experts and academic centres; this will involve participating in scientific congresses, coordinating advisory boards, round-table meetings, discussion fora etc.
Deliver scientific presentations and medical education programs to healthcare professionals
Screen relevant literature and other information from relevant scientific societies meetings and conferences and develop summaries of key messages for use within the Company (e.g. key areas of scientific/company interest, new trends in diagnosis, monitoring and treatments in the therapeutic area, etc.)
Deliver training to sales forces and other departments; develop and update relevant training materials.
Design and implement clinical research projects within defined standards and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological surveys, and PMOS studies).
Provide the required oversight to manage review, approval and conduct of IIS studies.
Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate (e.g. review new clinical study protocols, identifying potential investigators/sites, conducting feasibility surveys).
Review and preparation of promotional material.
Provide medical/scientific input into marketing strategy and key commercial initiatives.
Ensure compliance with all applicable national laws and regulations, guidelines, codes of conduct, company policies and procedures and accepted standards of best practice.
QUALIFICATIONS / EXPERIENCE REQUIRED:
Physician (Medical Degree) or Pharmacist with Medical Affairs experience preferred
PhD with extensive Medical Affairs experience will also be considered.
Strong understanding on relevant codes of practice (i.e. ABPI) and regulations.
Therapy area experience of biologics an advantage
Before you apply for this position it is vital that you are in possession of an EU or UK passport or relevant visa to work without restrictions in the UK.
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 6727.
BIOSIMILARS / Biosimilar Medical Lead / Medical Affairs Manager / Medical Manager / Medical Lead Biosimilar / Immunology / immunology / medical manager / scientific affairs / medical affairs / Medical Lead / Head of Immunology / Therapy Head / Immunology Lead / UK / Reading / Bracknell / Slough / Windsor / London
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,
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