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Clinical Research Scientist At Best Search Recruitment

Date Posted: 03/Apr/2014
Deadline: 30/Nov/-0001

Best Search Recruitment - Our client, a Multinational Pharmaceutical Company is in need of:

Clinical Research Scientist

Job Summary
Translating scientific and medical information, establishing and maintaining peer relationships with key opinion leaders (clinical/research leaders in assigned therapeutic areas) and developing educational materials and support programs for personnel.


  • Develop and maintain professional relationships with key opinion leaders and academic centers to ensure their access to current medical and scientific information.
  • Develop clear individualized stakeholder plans and a regional medical affairs strategy
  • Identify clinical investigators with research proposals that are consistent with our product development strategies and facilitate the investigator initiated research
  • Disseminate, review and present evidence-based data in an unbiased manner
  • Provide speaker training to health care professionals to support the best use of new therapies developed and commercialized.
  • Provide speaker training to health care professionals to support the best use of new therapies developed and commercialized.
  • Share field intelligence and competitor information with internal stakeholders and help to create actionable plans
  • Contribute to the identification of appropriate clinical investigators and facilitates placement into sponsored clinical trials.


  • Ph.D, Pharm.D, MD, in a healthcare or scientific discipline.
  • 3+ years industry experience
  • A high level of scientific expertise with a proven ability to interpret and effectively communicate complex clinical data.
  • Strong strategic thinking ability, operating with a sense of urgency to respond to business needs in a timely manner and solid business acumen.
  • Excellent interpersonal skills for successful cross-functional collaborations with internal partners is essential.
  • Demonstrated independence in managing assigned projects within established timelines.
  • Familiarity with all aspects of clinical trial processes.
  • Knowledge and adherence to local regulatory agency policies, Good Clinical Practices (GCP) guidelines.

Method of Application 
Interested and qualified candidates should send CVs to:[email protected]

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