Cra - Global Clinical Trials
4 days ago
**Responsibilities**
- Identifying investigators, perform feasibility and assessing sites with regard to protocol and local requirements.
- Acting as the main line of communication between the sponsor and the investigators.
- Training of investigator and the clinical site staff on all trial requirements & procedures.
- Assisting trial team with site budget negotiation and execution of site contracts.
- Conducting site visits and preparing monitoring reports (e.g. selections, initiation, periodic, close-out).
- Verification of source documents,IP accountability, lab data review etc.
- Willingness to travel for 15-16 days of month to various locations inIndia.
- Assisting with and/or prepare all necessary documentation for IEC/IRB and regulatory submissions.
**Job Requirements**:
- Bachelor's or Master's degree in Lifesciences.
- 3-4 years of experience & good understanding of clinical research.
- Excellent communication skills.
- Ability to be autonomous and self-motivated.
- Fluent in English.
- Travel required.
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