Medical Advisor - Interim pulmonary vascular disea
Date Posted: Wednesday, 22nd of February 2012
Salary: Competitive
Start Date: ASAP
Telephone: 01438743047
Location: South East
Discipline:Medical
Consultant Name: Moin Din
Description
Interim Medical/Scientific Advisor - Pulmonary Vascular Disease (PVD) - 23760
Reporting to the Medical Team Leader PVD, Europe, Scientific Advisers will be responsible for ensuring that all materials delivered to countries by the PVD Teams accurately communicate product knowledge, are appropriate for use and meet general technical standards for European markets.
Working within the cross-functional PVD Unit the Scientific Adviser will support the development of product promotion and communications strategies, information collation and provision to the European markets and review of promotional material. The Scientific Adviser will provide evaluated, balanced information about Pfizer products to key stakeholders and, through cross-functional team working, ensure that key marketing strategies and activities are successfully implemented to achieve business objectives. The Scientific Adviser will also be required to develop a detailed understanding of pan- European regulations and codes relevant to the promotion of human pharmaceuticals and act as an advisory resource for the SCBU brand teams. The Scientific Adviser will also support the Disease Area Review Committee meetings.
Responsibilities
Scientific, Operational and strategic support:
• As part of the cross-functional PVDU, actively participate in all activities designed to provide excellence in information provision and observance of regulations and company standards.
• Provide scientific expertise to thePVDU, generating insights and playing a key role in strategic planning to identify information gaps and options for generating evidence.
• Support the planning and development of promotional materials and medical educational activities (eg symposia^and congress activities, advisory boards etc) through data provision, evaluation and assessment of scientific content, ensuring that data are used and presented in an appropriate way whilst supporting the commercial needs of the European countries.
• Ensure the medical accuracy of materials, their compliance with product licenses and relevant codes of practice and that referencing is relevant and accurate.
• Generation of, provision and communication of information related to disease area
• Medical Education material generation for country medical teams eg slide kits, Q&As
• Operational excellence for medical activities eg IIR organisation and tracking etc
Qualifications
University degree in Science, Pharmacy or Health Sciences^(or equivalent).
Solid experience in healthcare, pharmaceutical or related field.
Highly motivated and proactive Scientist with solid knowledge of medical marketing, clinical research and regulatory requirements.
Bilingualism is an advantage,fluency in English required.
Knowledge and experience of the TA is preferable.
Requirements:
Experience of promotional review and sign-off in Europe.
Project management experience
Experience of using literature databases
Experience working with cross-functional teams.
Ability to critique, evaluate and communicate scientific data
Detailed oriented and attention to quality
CK Clinical is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL23760 in all correspondence.
