
Clinical Research Coordinator
1 day ago
**Responsibilities**
- Develop and maintain study protocols and case report forms.
- Recruit and screen study participants per study criteria.
- Obtain informed consent from study participants and explain study procedures.
- Collect and manage study data, including adverse events and other safety-related information.
- Monitor study participant compliance and follow-up visits.
- Manage study supplies, equipment, and inventory.
- Assist with preparing and submitting study-related documentation to regulatory agencies and institutional review boards.
- Collaborate with study sponsors and principal investigators to ensure that studies are conducted according to protocol.
- Communicate study progress to research staff and other stakeholders.
- Ensure that study data is collected and managed in accordance with regulatory requirements and study protocol.
**Requirements**:
- Bachelor's degree in a scientific or healthcare-related field
- Strong organizational and project management skills
- Excellent attention to detail and accuracy
- Strong communication and interpersonal skills
- Ability to work well under pressure and within strict timelines
- Knowledge of clinical research protocols, case report forms, and study procedures
**Job Types**: Full-time, Permanent, Fresher
Pay: ₹30,721.80 - ₹45,900.04 per month
**Benefits**:
- Health insurance
- Provident Fund
Schedule:
- Day shift
Supplemental Pay:
- Performance bonus
- Yearly bonus
**Experience**:
- total work: 1 year (preferred)
Work Location: In person
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