Clinical Research Coordinator
1 month ago
Records adverse event and side effect data and confers with investigators regarding the reporting of events to oversight agencies. Prepares for or participates in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Identifies protocol problems, informs investigators of problems, or assists in problem resolution efforts such as protocol revisions.
- Prepares study-related documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
- Participates in preparation and management of research budgets and monetary disbursements.
- Instructs research staff in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures.
- Collaborates with investigators to prepare presentations or reports of clinical study procedures, results, and conclusions. Communicates with laboratories or investigators regarding laboratory findings.
- Reviews scientific literature, participates in continuing education activities, and/or attends conferences and seminars to maintain knowledge of clinical studies affairs and issues.
- Orders drugs or devices necessary for study completion.
- Solicits industry-sponsored trials through contacts and professional organizations.
**Salary**: ₹25,800.11 - ₹30,679.08 per month
**Benefits**:
- Flexible schedule
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
Ability to commute/relocate:
- Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (required)
**Speak with the employer**
+91 8446600737
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