کارشناس مطالعات بالینی

آرتا فارمد تهران

منتشر شده 10 ماه پیش

Job Description

  • Coordinates clinical studies in the medical research area.
  • Develops an understanding of the requirements of the study protocol. Adheres to the protocol in all situations.
  • Responsible for recruitment, screening, interviewing, and evaluating of study participants.
  • Develops advertisement copy and recruitment plan for recruiting study participants.
  • Responsible for the development, completion, accuracy, and maintenance of patient forms, including Informed consent.
  • Completes or oversees the completion of data entry in a timely manner.
  • Monitors patient safety, compliance, and health status.
  • Anticipates study problems, formulates solutions, and determines resolutions.
  • Responsible for all aspects of study termination, i.e. completing necessary documents/forms, return of drugs to drug company, etc.
  • Develops and maintains communication with the research manager, co-workers, principal investigators, and other internal personnel regarding study related issues.
  • Participates in department staff meetings, study planning and special projects as appropriate.
  • Communicates necessary information with sponsors, monitors, patients, physicians, co-workers, and others in a courteous and professional manner.

Requirements

  • Ability to work in a collaborative, effective manner with all necessary research team members in order to meet the research objectives.
  • Able to be a liaison between physicians, drug companies, research organizations, staff, and patients.
  • Bachelor's or Master's degree from an accredited university in Nursing or Pharmacy.

Employment Type

  • Full Time

Details

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