September 14, 2025 – October 12, 2025
Every Sunday | 6:00–8:00 PM IST
Virtual | Live, trainer-led sessions
Unlock Your Pathway to a Career in Clinical Research
India’s clinical research industry is growing rapidly, offering rewarding career opportunities in
pharmaceutical
companies, clinical research organizations (CROs), and biotech firms. However, many aspiring
professionals
are unsure how to gain the right skills to enter the field.
This program is designed to bridge that gap by providing practical, industry-aligned training across
all major
aspects of clinical research. Participants will build a strong foundation in trial operations,
ethics and regulatory
guidelines, quality and compliance, pharmacovigilance, scientific writing, and more—empowering them
with
the knowledge and confidence to launch or transition into a successful career in clinical research.
Who Should Attend
- Early-career professionals in life sciences, pharmacy, or medicine
- Recent graduates exploring careers in clinical research or regulatory domains
- Professionals transitioning into the pharmaceutical, CRO, or biotechnology sectors
What You Will Learn
- Clinical trial processes and global regulatory frameworks (ICH-GCP, Indian guidelines)
- Trial operations, ethics, and documentation (protocols, informed consent, clinical study reports)
- Fundamentals of pharmacovigilance, materiovigilance, and scientific/medical writing
- Quality management, audit preparedness, data handling, and intellectual property essentials
About the Trainers
Dr. Shruti Shah, MSc, PhD
Director, Strategy and Growth
With over 20 years of experience, Dr. Shruti, the Technical Head, leads the review and management of publication writing, advisory boards, and congress presentation projects for major pharmaceutical companies. She also brings extensive expertise as a technical trainer in scientific and medical writing, medical affairs, and medico-marketing, where she has mentored professionals to develop into high-quality medical writers.
Vikas Salgotra, MPhil, PGDACR
Associate Director, Clinical Research
Vikas is a clinical researcher with over 10 years of experience managing clinical studies (Phase III, post-marketing surveillance, real-world evidence, first-in-man) across multiple therapeutic areas and medical devices. He is skilled in clinical operations, project planning, stakeholder engagement, and KOL management, while ensuring GCP compliance with a strong focus on driving best practices and operational excellence.
Ankita Sevkani, MPharm (Pharmaceutics)
Medical Writer
With over a decade of experience in medical writing and a proven track record in publication writing, developing real-world evidence and advisory board documents, and creating medico-marketing materials, Ankita combines her extensive industry knowledge with a passion for mentoring. She enables participants to gain practical insights and skills directly applicable to real-world scenarios.
Tanvi Goel, MPharm (Pharmaceutical Chemistry)
Medical Writer
Tanvi is an experienced regulatory medical writer with expertise in clinical study reports, protocols, narratives, investigator brochures, and systematic literature reviews across multiple therapeutic areas. With a strong background in clinical documentation and decentralized trials, she brings practical insights that help participants understand core clinical research processes and regulatory expectations.
Frequently Asked Questions (FAQs)
Q: Who can attend this course?
A:
The course is ideal for early-career professionals, recent graduates, and anyone
interested in entering or transitioning into the clinical research, pharmaceutical,
or regulatory sectors.
Q: Do I need prior experience in clinical research?
A:
No. Prior experience is not required. The course is designed for beginners as well
as those looking to build a solid foundation in clinical research and related fields.
Q: Will I get a certificate?
A:
Yes. All attendees will receive a certificate of completion.
Q: What if I miss a session?
A:
Session recordings will be available for six months.
Still have questions? We’re here to help!
+91-98101-50476
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