ASSISTANT CLINICAL RESEARCH COORDINATOR

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.