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.
Study Coordinators: Provides safety & protection while
collecting & managing the study data.
Data Manager / Biostatistician: Design, study & predict the
seriousness of the disease, seriousness of the disease, evaluate new treatments
and effectiveness of medication, participate in research design, data
collection, choosing & implementing appropriate methodologies, interpreting
the results.
Regulatory Affairs Managers: Review & registration of
documents, evaluation of technical data, liaison with regulatory authorities.
Clinical Trials Auditors: Conducts audits for regulatory
function within the trial department to assure compliance with GLP/GCP in
accordance with established FDA regulations and company policies & standard
operating procedure.
Clinical Data Manager: Ensures the accuracy & consistency in
data prepared for regulatory bodies for reporting purpose.
Others: Auditors, Quality Assurance, Patents & IP Related
position