Study Coordinator

Job details

Contract Type

Description

Qualification Required:

  • BACHELORS : MBCHB - Mandatory
  • MASTERS : Msc in basic sciences such as Pharmacology, or Physiology - Added Advantage


Responsibilities
  • Ensure efficient study implementation, regulatory compliance, data quality, and coordination across clinical and laboratory teams.
  • Ensure compliance with national and institutional ethical guidelines
  • Maintain study regulatory files (IRB approvals, consent forms, protocol amendments
  • Participate in patient pharmacokinetic (PK) evaluations
  • Ensure coverage and assist in daily operations in the clinic during working hours (8:00 a.m. to 5:00 p.m.)
  • Supervise study staff including Clinical Officers, nurses, home visitors, and Laboratory personnel
  • Participate in regular team meetings, and training sessions
  • Oversee data collection, entry, and validation processes
  • Monitor completeness of participant follow-up and minimize loss to follow-up
  • Coordinate procurement and distribution of study supplies (lab materials, drugs, participant refunds)


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