Clinical Research Coordinator
3 months ago
**Job Summary**
We are looking for a highly motivated and detail-oriented Entry-Level Clinical Research Coordinator (CRC) to join our clinical research team. This role is ideal for recent graduates or individuals with limited professional experience who are passionate about starting a career in clinical research. The CRC will assist in managing clinical trials, coordinating activities at research sites, and ensuring compliance with study protocols and regulatory requirements.
**Key Responsibilities**
- **Study Coordination**:
- Assist in the planning and execution of clinical trials, including site preparation and patient recruitment.
- Coordinate study-related activities, such as scheduling patient visits, collecting data, and ensuring the timely completion of study tasks.
- **Documentation and Compliance**:
- Support the preparation and maintenance of essential documents for clinical trials, including regulatory submissions, informed consent forms, and study manuals.
- Ensure that all documentation is accurate, complete, and in compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
- **Site Management**:
- Assist in the training of site staff on study protocols and procedures.
- Facilitate communication between the research team and study participants, addressing any questions or concerns they may have.
- **Data Collection and Management**:
- Help in the collection, entry, and management of clinical trial data, ensuring accuracy and completeness.
- Assist in monitoring data quality and resolving any discrepancies or issues.
- **Regulatory Affairs**:
- Aid in the submission of required documentation to Institutional Review Boards (IRBs) or Ethics Committees.
- Ensure that all regulatory requirements are met and maintained throughout the trial.
**Qualifications**
- **Education**:
- Bachelor’s degree in Life Sciences, Nursing, or a related field. Coursework or training in clinical research is a plus.
- **Experience**:
- No prior professional experience required. Internships, volunteer work, or academic projects related to clinical research are beneficial.
- **Skills**:
- Strong interest in clinical research with a willingness to learn.
- Basic understanding of clinical trial processes and regulatory requirements is an advantage.
- Excellent organizational and communication skills, with a keen eye for detail.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- **Other Requirements**:
- Ability to work independently and as part of a team in a dynamic environment.
- Willingness to travel to clinical sites as needed (may include occasional overnight stays)
**Job Type**: Fresher
Pay: ₹11,400.38 - ₹31,213.30 per month
Schedule:
- Day shift
- Morning shift
**Experience**:
- total work: 1 year (preferred)
Work Location: In person
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