Vacancies

Summary

Assists and coordinates clinical research daily tasks required for research and/orclinical protocol; assists in a variety of complex activities involved in thecollection, compilation, documentation and analysis of clinical research dataunder the direction of a Principal Investigator or Project Leader.

Essential Responsibilities and Duties

1. Assists in the daily clinical research studies and ensuresits efficient compliance with protocols’ objectives.

2. Obtains patient consent, schedules appointments, andextracts medical information from patient charts, and other sources into casereport forms and/or online database as required by the study protocol.

3. Monitors human subjects’ protocols, and prepares progress/finalreports and adverse event reports according to the Hospital’s Office ofResearch Affairs (ORA) procedures.

4. Assists in recruiting patients, collecting clinical samples,recording vital signs, filling up questionnaires, developing forms, and otherdocumentation required for the project. 

5. Facilitates collection of data from patient charts, medicalrecords, interviews, questionnaires, diagnostics tests and other sources; helpsin coding, evaluations and interpretation of collected data and preparation doof appropriate documentation.

6. As applicable, contacts patients or their families to ensureappointment for treatment and/or follow-up review.

7. Assists in performing regular research project’scommunications, recordkeeping and administrative duties.

8. Supports in the preparation and management of researchbudgets and monetary disbursements.

9. Provides assistance to the Clinical Research team andensures timely completion of tasks.

10. Follows all Hospital related policies and procedures.

11. Participates in self and others’ education, training anddevelopment as applicable.

12. Performs other related duties as assigned. 

Education

Bachelor’sor Associate Degree/ Diploma in a clinical field such as Nursing, Pharmacy orany field related to health sciences is required.

Experience Required

Two (2) years of Clinical, Healthcare and/or relevant research experience withBachelor’s or four (4) years with Associate Degree/ Diploma is required.

Other Requirements(Certificates)

• Saudi National Only.  
• A certificate of completion of the NIH (National Institutes of Health) web-based training course: “Protecting Human Research Participants” is preferred.
• A successful completion of either a Clinical Research Professional course (offered in house) or any other accredited online course is preferred.