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Fforde Management
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Senior Clinical Research Physician - Diabetes



Business Type: Clinical Research Organisation
Job Type: Clinical Research, Clinical Study- Trials, Clinical Physician
Job Level: Not Specified
Position: Full Time
Salary: Competitive
Location: UK - South East
Reference: 15810/003
Closing Date: 02/08/12
Background:
Our client is committed to developing a growing portfolio of superior pharmaceutical-based health care solutions with breakthrough medicines for conditions such as depression, schizophrenia, attention-deficit hyperactivity disorder, diabetes, osteoporosis and many more. They are currently seeking a Senior Clinical Research Physician to be office based in the South East.

JOB ROLE:
Working specifically within the Diabetes Medical Team working closely with the Senior Medical Advisor this is a medical position responsible for sign off and full approvals. The Snr CRP will be acting as the main medical advisor for the brand and sales teams and providing the medical input into the strategy for the insulin portfolio.

PRINCIPAL RESPONSIBILITIES include:
Provide medical expertise in relevant therapeutic area(s) to the United Kingdom (UK) / Republic of Ireland (ROI) affiliate, regional and global teams
Develop effective partnerships with relevant internal functions
Develop effective partnerships with clinicians, other key influencers KOL''s and external groups
Provide visible leadership to other members of the Medical Department and the broader affiliate
Manage Medical Liaisons (MLs) as determined by the business need
100% compliance with the relevant global and local curriculum maps, including GPP
Review and Certification of materials for medical accuracy and compliance with the Association of the British Pharmaceutical Industry (ABPI) Code of Practice and Medicines and Healthcare products Regulatory Agency (MHRA)
Drive the response to challenges from competitors, the ABPI and the MHRA within the predetermined timelines
Contribute to Regional Planners and Global Brand Council (or equivalent) process
Provide medical leadership
Take accountability for the appropriateness of, objectives for, and content of Advisory Boards
Provide strategic medical input into wider business decisions
Provide leadership within the Medical Department
Drive process of UK and ROI Clinical Trial (CT) selection from the Global and Regional plan
Input into the development of Global and Regional CT plans
Implement, in consultation with the Clinical Operations Manager (COM), the Global / Regional CT plan with Quality Speed and Value
Develop and implement a local CT plan
Participate in site selection, start-ups, site issue resolution and Plan Do Review (PDR) meetings
Identify and engage with Health Care Professionals (HCPs), Advocacy Groups, government and other professional bodies as determined by business needs

QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
Basic medical degree plus higher medical qualification
Full GMC or equivalent registration through revalidation
Input into regulatory submissions and Health Technology Assessments (HTAs)
Assist Medical Information and Global Product Safety UK as requested, including out of hours calls
Drive and take accountability for the process and content of scientific publications
Provide initial and ongoing disease, product and competitor training for employees in conjunction with the Training Department
Provide presentation to groups
Participate in the production of materials with substantial or critical medical content (e.g. detail aids, clinical slide sets etc.)
Maintain and grow therapeutic and management expertise
Maintain and grow pharmaceutical medicine expertise through the Diploma in Pharmaceutical Medicine and HMT



Fforde is acting as a recruitment agency/business.


KEY WORDS: Clinical Research Physician, CRP, GMC, Medic, physician, MD, medical doctor, submissions, Advisor boards, Diabetes, ABPI, MHRA, regulatory, advisory, clinical trials, pharmaceutical, drug development, drug safety, HTA, Health Technology Assessment, South East, UK.


Posted: 05/07/2012 | NPJ Ref: 83735
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