Clinical Research Associate

Job highlights

• Verifying data sources,and reviewing regulatory documents / files to ensure that documents are in compliance with protocols,regulatory requirement. SOPs (standard operating procedures),and are aligned with the Monitoring Plan.

JOB DETAILS

1. Performing routine data collection from patients,

2. Verifying data sources, and reviewing regulatory documents/files to ensure that documents are in compliance with protocols, regulatory requirement

3. SOPs (standard operating procedures), and are aligned with the Monitoring Plan.

4. Some clinical research associates assist in reviewing study protocols, informed consent forms, and case report forms.

5. They may also participate in developing monitoring plans, abstracts, presentations, manuscripts and clinical study reports under supervision.

6. Clinical Research Associates manage clinical trials and studies pertaining to biotechnological and pharmaceutical products, drugs and procedures.

7. Conducts research to ensure these products are safe.

8. Responsible for site follow up activities in order to maintain documents..

9. Complete accurate study status reports

10. Participate in training and mentoring new staff up to Clinical Research Associate level as appopriate
    FUNCTIONAL AREA
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