Clinical Research Trainer
2 days ago
**Responsibilities**:
- Develop and deliver training on Clinical Research, Clinical Data Management (CDM), Pharmacovigilance (PV), and Good Clinical Practice (GCP), with additional knowledge of Medical Writing (MW) and Regulatory Affairs (RA) as a plus.
- Conduct assessments and provide feedback to improve trainees’ clinical research skills.
- Stay updated on industry regulations and incorporate changes into training materials.
- Support trainees in job preparation and placement efforts.
- Maintain training records and foster an engaging learning environment.
**Qualifications**:
- Experience as a Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) is mandatory.
- 3+ years in clinical research, pharmacovigilance, or data management.
- Strong knowledge of clinical trial phases, safety reporting, and regulatory requirements.
- Excellent communication and presentation skills with hands-on teaching experience.
- Bachelor’s or master’s degree in Clinical Research, Life Sciences, or a related field is preferred.
**Job Types**: Full-time, Permanent
Pay: ₹50,000.00 - ₹70,000.00 per month
**Benefits**:
- Provident Fund
Schedule:
- Day shift
Supplemental Pay:
- Yearly bonus
**Experience**:
- total work: 2 years (required)
Work Location: In person
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