Clinical Research Coordinator
2 weeks ago
**Study Coordination**:
- Coordinate all aspects of clinical research studies, including participant recruitment, enrollment, and retention.
- Schedule study visits, procedures, and assessments in collaboration with study team members.
- Ensure that all study procedures are conducted according to protocol requirements and regulatory standards.
- Collect, record, and maintain accurate and complete study data in accordance with Good Clinical Practice (GCP) guidelines.
**Regulatory Compliance**:
- Assist in obtaining regulatory approvals, including Institutional Review Board (IRB) submissions and informed consent processes.
- Maintain regulatory documentation, including study protocols, investigator brochures, and study-related correspondence.
- Ensure compliance with regulatory requirements, institutional policies, and sponsor-specific guidelines.
**Participant Interaction**:
- Screen and assess potential study participants for eligibility criteria.
- Obtain informed consent from participants and provide education about study procedures and expectations.
- Serve as a point of contact for participants, addressing questions, concerns, and adverse events throughout the study.
**Study Administration**:
- Coordinate study-related logistics, such as ordering supplies, managing study budgets, and organizing study-related meetings.
- Assist with study monitoring visits, audits, and inspections by regulatory agencies or sponsors.
- Maintain study documentation and files in accordance with regulatory and institutional requirements.
**Collaboration and Communication**:
- Collaborate effectively with interdisciplinary team members, including physicians, nurses, pharmacists, and laboratory personnel.
- Communicate study progress, issues, and updates to study team members, PIs, and sponsor representatives.
- Foster positive relationships with study participants, ensuring their safety, well-being, and satisfaction throughout the study duration.
Pay: ₹12,000.00 - ₹18,000.00 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Day shift
Supplemental pay types:
- Performance bonus
**Experience**:
- total work: 1 year (required)
Work Location: In person
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