Clinical Research Associate -Reputed Clinical Industry -Delhi, NCR, India -6LPA -Kajal

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...