✔ Clinical Research – Overseeing the design, planning, and implementation of clinical trials to assess new drugs and therapies.
✔ Clinical Data Management – Ensuring the accurate collection, validation, and management of clinical data throughout a trial to maintain quality and integrity.
✔ Medical Writing – Creating regulatory documents, clinical trial reports, and manuscripts that communicate clinical trial results and research findings.
✔ Pharmacovigilance – Monitoring and evaluating the safety of drugs and medical products, identifying adverse effects, and ensuring compliance with regulatory standards.
✔ Regulatory Affairs – Assisting in drug approval processes, ensuring clinical trials and drug safety protocols meet global regulatory standards.
Our program is open to candidates with the following academic backgrounds:
- Pharmacy: B.Pharm, M.Pharm, Pharm.D
- Science: B.Sc., M.Sc., Ph.D. in Biotechnology, Microbiology, Biochemistry, Nursing, and related fields
- Engineering: B.E., B.Tech., M.Tech. in Biotechnology or Biomedical Engineering
- Medical & Health Sciences: BPT, MPT, BDS, BAMS, BHMS, MBBS
For Science, Life Science, and Medical Candidates:
✅ High Demand: Rising demand for clinical research professionals in pharmaceutical, biotechnology, and healthcare sectors.
✅ Specialization: Work in drug development, clinical data management, and pharmacovigilance.
✅ Global Opportunities: Opportunities to work with leading pharmaceutical companies, CROs (Contract Research Organizations), and regulatory bodies globally.
✅ Lucrative Career: Clinical research and pharmacovigilance professionals are highly sought after, with competitive salaries and growth potential.
For Medical & Healthcare Professionals:
✅ Focus on Drug Safety: Direct involvement in ensuring the safety and efficacy of drugs through pharmacovigilance.
✅ Contributing to Patient Safety: Play a key role in tracking adverse drug reactions and ensuring regulatory compliance.
Pharmaceutical and Biotechnology Companies: Conduct clinical trials, manage drug safety data, and create regulatory submissions.
CROs (Contract Research Organizations): Provide clinical trial management services to pharmaceutical companies.
Regulatory Authorities: Help monitor compliance with global standards and regulations for new drugs and therapies.
Healthcare & Medical Research Organizations: Design, monitor, and report on clinical studies for new medical treatments.
Global Opportunities: Work with top pharmaceutical firms, healthcare organizations, and regulatory bodies worldwide.
Lucrative Salaries: Starting salaries range from INR 4 LPA to INR 8 LPA for freshers, with experienced professionals earning INR 10 LPA to INR 20 LPA based on specialization and expertise.
Career Growth: Rapid advancement opportunities as clinical research and pharmacovigilance become essential components of drug development and safety.
Freshers can expect a starting salary between INR 4,00,000 and INR 7,00,000 per annum.
Experienced professionals can earn anywhere between INR 8,00,000 and INR 20,00,000 or more per annum, depending on expertise and role.
✔ High Relevance: Contribute to cutting-edge medical research, patient safety, and drug development.
✔ Evolving Industry: The global healthcare sector continues to expand, increasing the demand for clinical research and pharmacovigilance professionals.
✔ Job Security: These roles are critical in the pharmaceutical and healthcare industries, ensuring long-term career stability.
Clinical Research Associate (CRA)
Clinical Data Manager
Pharmacovigilance Associate
Medical Writer
Drug Safety Associate
Clinical Trial Assistant (CTA)
Regulatory Affairs Associate
Clinical Research Coordinator (CRC)
Pharmacovigilance Specialist
Safety Reporting Analyst
