Clinical Trial Assistant
6 months ago
**Key Responsibilities**:
- Assist in the maintenance, tracking, and filing of essential trial documents, including but not limited to study protocols, investigator brochures, informed consent forms, regulatory submissions, and site-specific documents.
- Support the implementation and adherence to regulatory requirements, GCP (Good Clinical Practice) guidelines, and company SOPs (Standard Operating Procedures) throughout the trial lifecycle.
- Coordinate and facilitate communication between investigative sites and the study team, including the distribution of study-related materials, collection of site regulatory documents, and resolution of site queries.
- Collaborate with the data management team to ensure accurate and timely data collection, entry, and query resolution, maintaining data quality and integrity.
- Assist in scheduling and organizing study team meetings, investigator meetings, and other trial-related events, including preparing meeting agendas, minutes, and follow-up actions.
**Qualifications**:
- Bachelor's degree in a scientific or healthcare-related field preferred.
- Prior experience in clinical research or healthcare administration preferred.
- Familiarity with regulatory requirements and GCP guidelines.
- Strong organizational skills and attention to detail.
- Excellent written and verbal communication skills.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
**Job Types**: Full-time, Permanent, Fresher
**Salary**: ₹18,987.65 - ₹40,867.53 per month
**Benefits**:
- Cell phone reimbursement
- Health insurance
- Provident Fund
Schedule:
- Fixed shift
- Morning shift
Supplemental pay types:
- Performance bonus
- Yearly bonus
Work Location: In person
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