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 Associates: To monitor clinical trials, ensure compliance
with the clinical trial protocol, checks clinical sites activities, make on-site visits,
CRFs.
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 treatment 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 Research Managers: Manage, supervise, train, mentor clinical
research staff, approve investigator’s study, budget & contract, review & approve
regulatory documents, develop a protocol, approve CRFs, review study data.
Business Development Manager: Identify potential clients, establish
business relations, responsible for meeting new clients, following up on leads, market
research.
Drug Safety Associate: Manage & relay drug safety information, maintain
current knowledge of global drug safety regulations, summarize clinical safety data, write
narratives with medical input, report SADRs to Regulatory Authorities, participate in
training on drug safety issues & another task under drug safety.
Medical Writer: Documentation, manuscripts, abstracts, external
communication tools Clinical Data Manager: Ensures the accuracy & consistency of data
prepared for regulatory bodies for reporting purpose.
Others: Auditors, Quality Assurance, Patents & IP Related position