Clinical Research Associate

1 week ago

Noida, India Seven Consultancy Full time

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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