3 years

4 - 5 Lacs

Bengaluru

Posted:1 week ago| Platform:

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Skills Required

training research data management pharmacovigilance gcp writing regulations support learning reporting communication presentation teaching sas

Work Mode

On-site

Job Type

Full Time

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

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