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Head of Clinical Research - EVA Pharma



Eva Pharma; a company who fights for health and wellbeing as a human right, a multinational pharmaceutical company operates in more than 40 Countries, having a diverse top team of more than 3000 professional associates across the globe is seeking a hands-on Clinical Trials Consultant who is a proactive team player interested in driving in a clinical research activities within a fast-growing, dynamic, collaborative company with KPIs to support our international markets as well. The candidate should have a solid experience in clinical trial activities in different therapeutic areas.

Main Tasks and Responsibilities:
  • Responsible for overlooking research site management for studies in accordance with1` Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures.
  • Oversee completion of study activities per protocol.
  • Ensure that study protocol is in compliance with appropriate rules & regulations
  • Draft the study protocols
  • Review study progress and recommends revisions, amendments, and/or other study changes as necessary to better meet needs of sponsors.
  • Analyse, evaluate & interpret data to determine relevance to research.
  • Liaise with Health Care Professionals (HCPs) and educational institutions and eminent Professors in Medical Affairs events and trainings in almost all Therapeutic Areas.
  • Supervise and Maintain the overall Research Budget in accordance with the annual approved amount.
  • support in scientific advices with local regulatory authorities to get clearance on the study requirments

If you are expert in the above Responsibilities with evidence, we will have the pleasure to receive your application. 

  • Medical Academic Background, Preferably Physician/Pharmacist.
  • Minimum of 10 years working in Clinical Research / Clinical Trial Consultancy.
  • Dealing with EMA/FDA in Clinical Research Phase1, 2, 3 bioequivilance studies as well as dealing with further studies which are necessary to get approvals for patches or other dosage forms is a very big asset
  • Strong network of opinion leaders across market segments.
  • Supervisory or project management experience required.

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