Job Details

Clinical Research Coordinator


Job Title:

Clinical Research Coordinator



Clinical based Company in Riyadh






Riyadh, -


The Role

Serves as primary study coordinator for research protocols at affiliated hospitals or in the outpatient clinic setting as assigned by Director. Directs the conduct of clinical studies to ensure adherence to the research protocol and provides bimonthly updates to Principal Investigator on study progress. Screens patient records, databases, and physician referral summaries for identification of prospective candidates for research protocols. Interviews prospective subjects for participation in investigations and obtains informed consent. Participates in initiation visits/investigator’s meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor. Develops study working folders for assigned protocols to outline guidelines for protocol compliance and to assure complete source documentation. Educates human subjects for participation in investigations. Educates clinic/hospital personnel for participation in protocol conduct, data collection process, and related conceptual issues as applicable. Maintains consistent enrollment in protocols and provides monthly written documentation of screening/enrollment/follow-up activities. Coordinates the collection of data according to the research protocol, operations manual, and case report form guidelines within the budgetary guidelines established by Director. Draws, prepares, and ships laboratory samples for clinical trials. Maintains investigational drug/device dispensing accountability and shipping logs according to protocol guidelines.

Skill Set/Qualification

Bachelors Degree in a Healthcare or Clinical Research related field required; Masters Degree in a Healthcare or Clinical Research related field preferred Minimum 5+ years of practical work experience acceptable in lieu of education. Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA), preferred; Proficient in word processing, computer spreadsheets, mainframe computer applications, and database management. Ability to prioritize and organize a high volume workload and changing priorities.