Company: MediPharma Konnect
Required Asst Manager - Quality Assurance with Clinical research Organization @ Ahmedabad
Work Exp - 3 to 4 years as CRC or working as QA
CTC - Up to 4.00 LPA
Roles and Responsibilities:
1. Liaising with doctors/consultants (or investigators) on conducting the trial;
2. Monitoring the trial throughout its duration, which involves visiting the study centers on a regular basis;
3. Verifying that data entered onto the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV);
4. Review the Laboratory and patient data, Concomitant medications, AEs and SAEs, Regulatory reporting requirements and Notification letters to regulators/investigators/IRBs
5. Discuss results with the study team leaders.
Mail id - medipharma.resume@gmail.com
Call / Whatsapp - 7048451451
Medi Pharma Konnect
(One-stop solution for Pharma & Healthcare)
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