Job Description

Roles & Responsibilities

1. Assists in the daily clinical research studies and ensures its efficient compliance with protocols objectives.

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

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

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

5. Facilitates collection of data from patient charts, medical records, interviews, questionnaires, diagnostics tests and other sources; helps in coding, evaluations and interpretation of collected data and preparation do of appropriate documentation.

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

7. Assists in performing regular research project s communications, recordkeeping and administrative duties.

8. Supports in the preparation and management of research budgets and monetary disbursements.

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

10. Follows all Hospital related policies and procedures.

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

12. Performs other related duties as assigned.

Desired Candidate Profile

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

Two (2) years with Bachelor s, or four (4) years of related experience with Associate Degree/ Diploma is required.