Certificate in Clinical Operations

Course Duration : 3 Months

Minimum eligibility criteria for application to the course would be either of the following:

MBBS
BAMS
BDS
BHMS
Physiotherapy and Occupational Therapy Graduates
B.Pharm
M.Pharm & Graduates
Post Graduates in Sciences
Life sciences
BioSciences with any of the following subjects-Chemistry, Botany, Zoology, Biochemistry, Microbiology, Genetics and Biotech.

Study of Clinic management can be pursued after any bachelor degree with minimum 50% score. The programme has been in demand from last 15 years & has receiving highest number of applications from candidates with Arts, Psychology and teaching background. The course presents wide career prospects not only in India but also in abroad and is much appreciated by foreign universities as well.

Module I – Introduction to Clinical Operations

Module II – Basic Clinical Data Management

Module III – Clinical Trial Management

Module IV – Ethical Guidelines in Clinical Research

Module V – Ethics in Clinical Research

For Doctors: Principal Investigators / Co-investigator / Medical Advisor / Drug Developers / Regulatory Affairs Manager / Clinical Research Physician

For Paramedics, Pharmacists & Life Science Graduates: Medical Writers / Clinical Research Associates / Site coordinators / Clinical Research Manager / Drug Development Associates / Clinical Data Management / Pharmacovigilance Executive / Clinical Trail analyst / Drug Reviewer / Drug Safety Physician & many more.

For Management Professionals: (with Life Science/Health Science background): -Business Development / Clinical Project Management / Clinical Research Management / Regulatory Affairs Clinical Research Investigators: Conduct BA/BE studies, writing / revising SOP, review of protocols, investigators brochures, ICF & CRFs Protocol, CRF & ICF preparations plans and conduct of BA/BEIEC/IRB affairs-GC.

For Management Professionals: (with Life Science/Health Science background): -Business Development / Clinical Project Management / Clinical Research Management / Regulatory Affairs

Clinical Research Investigators: Conduct BA/BE studies, writing / revising SOP, review of protocols, investigators brochures, ICF & CRFs Protocol, CRF & ICF preparations plans and conduct of BA/BEIEC/IRB affairs-GC.