Qualification: B. Pharm with PG diploma in Clinical Research / M. Pharm / Masters in Clinical Research.
Experience: Experience: 2-3 years of experience in Clinical Research / Bioavailability & Bioequivalence Studies / CRA / CRC
Job description :-
1. Monitoring of outsourced bioavailability & bioequivalence studies Good Clinical Practices (GCP), Good Laboratory Practices
2.To perform Site Selection Visits, Site Initiation Visit, Site Monitoring Visit and Site Closeout Visit for patient based outsourced pharmacokinetic studies.
3. Review E-CRFs and electronically captured source data.
4. Verify the Trial Master Files for content and completeness at the clinical/investigator sites and manage/maintain the Trial Master Files for the sponsor. 5. Co-ordinate with Sponsor and CROS/Investigator sites for study monitoring activities and updates.
Send in your resume
to: Rosemary.varghese@sunpharma.com
