Immediate openings for Medical Investigator in Clinical Research (BA/BE studies)

Experience: 0-3 years experience in Clinical Research Industry.

*Freshers can also be considered

Work Location : Cherlapally, Hyderabad.

Primary Responsibilities:

1. Ensures that Valuable Clinical Practices (GCP) are followed.
2. Conduct planned studies as per protocol requirements, quality system procedures and SOPs.
3. Review of pre study health records.
4. Obtain written informed consent before each Volunteer participation in the trial.
5. Ascertaining that clinical data is complete, accurate and is recorded as per protocol and SOP requirements.
6. Assessment and documentation of UDS reports & additional test reports.
7. Documentation of eligibility status.
8. Verification of daily Temperature log , Urotherm reading , Emergency medication kit documentation and expired medication discarding.
9.



Briefing research staff on conducting the trail and Group briefing of ICF to volunteers
10. AE, SAE management, reporting and documentation.
11. Monitoring the trial throughout its duration.
12. Verifying the data entered on to the CRFs is consistent with source data.
13. ICU maintenance including management of emergency conditions.
14. Monitoring of Vitals documentation, ECG, Phlebotomy and X-ray procedures.
15. Verification of X ray films and X ray report destruction.
16. Post study reports assessments and documentation.

Completion status of CRFs and documentation Interested candidates can share their resumes to [email protected]

📌 Medical Investigator in Clinical Research @Vimta Labs Ltd, Cherlapally (Hyderabad)
🏢 Vimta Labs
📍 Hyderabad