Expert knowledge of ICH-GCP, Schedule Y and applicable regulatory requirements
Delivering lectures for Clinical Operations, Medical Writing, Clinical Data
Management, Pharmacovigilance and any other Clinical Research topic that may be
assigned.
Scheduling, planning and coordinating of lectures, exams, results for PT / FT / Distance
/ Online for CR and Regulatory Affairs courses
Ensure smooth completion of all batches and program structure of each course is
followed completely.
Placement tie ups with appropriate companies, generating placements to all CR & RA
students. Developing strong placement file.
Required Education:
Life Science Graduate PG / Masters in Clinical Research.
Required Experience:
2 to 3 yrs of Clinical Research Experience
- Experience2 - 3 Years
- No. of Openings1
- EducationAdvanced/Higher Diploma, B.Pharma, Post Graduate Diploma, M.B.A/PGDM, M.Pharma
- RoleClinical Research Trainer
- Industry TypeHospitals / Medical / Healthcare Equipments
- Gender[ Male / Female ]
- Job CountryIndia
- Job TypeWork from Office