Job Description

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: ₹450,000.00 - ?550,000.00 per year

Benefits:

Health insurance Provident Fund
Schedule:

Day shift
Education:

Master's (Required)
Experience:

SAS: 2 years (Required) Teaching: 2 years (Required)
Work Location: In person