Posted:2 months ago| Platform: SimplyHired logo

Apply

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

Mock Interview

Practice Video Interview with JobPe AI

Start Job-Specific Interview
cta

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.

Job Application AI Bot

Job Application AI Bot

Apply to 20+ Portals in one click

Download Now

Download the Mobile App

Instantly access job listings, apply easily, and track applications.

coding practice

Enhance Your Skills

Practice coding challenges to boost your skills

Start Practicing Now

RecommendedJobs for You