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PG Diploma in Clinical Research
PG Diploma in Clinical Research
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Clinical Research is a field that deals with the study and analysis of people’s health and illness. Overall, it is the means to which scientists analyze prevention, diagnoses and illness treatments. Clinical research study specifically focuses on improving disease knowledge, methods of developing diagnoses, new treatments or medical devices ensuring better care for patients. The field of study depends on a very framed and respects a precise study which is only realized under certain protocols of research.
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Benefits of PG Diploma in Clinical Research Training Program
Develop expertise in complex trial operations, from protocol design and investigator site management to regulatory submissions and safety reporting. Master advanced methodologies including adaptive trial designs, risk-based monitoring, and pharmacovigilance signal detection. Work with EDC systems, CTMS platforms, eTMF documentation, and CDISC data standards used across global trials. Build a professional portfolio with protocol development, monitoring plans, regulatory dossiers, and safety case reports. Get placement support for roles in trial management, regulatory affairs, and drug safety across leading research organizations.
Want to become a Clinical Research Professional?
Why PG Diploma in Clinical Research from CliniLaunch?
Comprehensive Curriculum
- High-quality Course Materials
- In-depth Learning Content
- Industry-relevant Modules
Industry-Driven Projects
- Hands-On Practical Experience
- Real-world Case Studies
- Direct Industry Applications
Expert Faculty
- Subject Matter Experts
- Industry Instructors
- Dedicated Faculty & Mentors
Flexible Learning Options
- Live Interactive Sessions
- Access to LMS
- Self-paced learning Modules
Career Support Services
- Job Placement Assistance
- Interview Preparation Guidance
- Resume Building Workshops
What is the Cost of Postgraduate Diploma in Clinical Research?
Course Fees
Online/Offline/Hybrid
Key Details of the Course
- 12-month instructor-led training
- Placement Support
- Industry Driven Curriclum
- Guest Speaker Networking Opportunities
- Study Material and Resources
Monthly Batches
Regular classes and weekend classes starts every month on 8th, 15th, 22nd, & 30th”
₹1,20,000
Invest in Your Soft Skills
Count on corporate training starting today
Customized Corporate Sessions
- Corporate Etiquette Training
- Mock Test/Interview Preparation
- Resume Building
- Placement Mentorship Program
- Networking Sessions
What is the Cost of AI & ML in healthcare?
Course Fees
Online/Virtual/Offline
Sessions to keep you job-ready
What you need to get started
- 12-month instructor-led training
- Industry-Driven Curriculum
- Study Material and Resources (LMS)
- Daily/Weekly Assessments
- Guest Speaker Networking Opportunities
- Placement Opportunities
Upcomming Batches
Regular classes and weekend classes starts on 8th,15th,22nd & 30th
₹1,50,000
Invest in Your Soft Skills
Count on corporate training starting today
Customized Corporate Sessions
- Corporate Etiquette Training
- Mock Test/Interview Preparation
- Resume Building
- Placement Mentorship Program
- Networking Sessions
CTA: Book a Free Demo
PG Diploma in Clinical Research Program Syllabus
Curriculum Designed by Experts
Learn to communicate in corporate settings, enhancing your workplace interactions and networking abilities.
Acquire essential skills to crack the interview with aptitude tests which is crucial for securing positions in clinical research and related industries.
Understand the fundamentals of drug actions and interactions to evaluate and develop pharmaceutical products.
Explore the monitoring and assessment of drug safety focusing on adverse reporting and risk management to ensure better public health.
Develop proficiency in drafting clear and concise medical documents, including research papers, regulatory submissions, and patient education materials.
Master the organization process, analysis, and clinical trial data validation, ensuring accuracy and compliance with regulatory standards.
Gain insights into the design, conduct, and oversight of clinical research studies, emphasizing project management and team coordination.
Explore the regulatory requirements governing the development, approval, and marketing of pharmaceutical products, ensuring compliance with laws and guidelines.
Draft comprehensive study protocols outlining research objectives, methodologies, and ethical considerations for clinical trials.
Acquire skills in systematic data collection methods and statistical analysis techniques, crucial for deriving meaningful insights from research findings.
Adhering to legal and ethical standards in drug development and healthcare, ensuring alignment with government regulations and industry guidelines for quality assurance.
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Industry Programs Offered in Collaboration with IBM Integrated with PG Diploma in Clinical Research
We offer the following industry-recognized programs in partnership with IBM as part of our PG Diploma in Clinical Research course. Delivered through the IBM LMS, these modules equip learners with enterprise-grade competencies in database performance, project management, and network security, supporting advanced research data operations in clinical environments.
IBM Course Name |
Guided Lab |
|---|---|
Project Management Fundamentals
|
Improving Performance with Indexes in MongoDB
|
Network and Database Security Fundamentals
|
Using an HTTP API to Create and Query IBM Cloudant Databases
|
NoSQL and DBaaS 101
|
Using the CQL Shell to Execute Keyspace Operations in Cassandra
|
Topics to be Covered in PG Diploma in Clinical Research Course
- EDC
- CTMS
- eTMF
- SAS
- Clinical Data Management
- Data Analysis
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PG Diploma in Clinical Research – Course FAQs
Graduates from life sciences, pharmacy (B.Pharm, M.Pharm, Pharm.D), medicine (MBBS, BDS, BAMS, BHMS), nursing (B.Sc/M.Sc Nursing), biotechnology, microbiology, biochemistry, or related disciplines are eligible. Healthcare professionals and clinical coordinators seeking career advancement can also apply.
This is a 12-month postgraduate program offered in online, offline, and hybrid modes. Designed for working professionals, fresh graduates, and career switchers, it provides flexible learning without disrupting current commitments.
Upon successful completion, you will receive a PG Diploma in Clinical Research accredited by NSDC and Brit Qualis, certifying your expertise for senior roles in pharmaceutical companies, CROs, and regulatory agencies.
The program covers advanced trial operations including pharmacovigilance, biostatistics, regulatory affairs, and project management. It includes hands-on training with EDC systems (Medidata Rave), CTMS platforms, eTMF tools, and safety databases through real trial simulations and regulatory submission projects.
Interested candidates can apply through the official website. After submission, a program counselor will contact you for eligibility verification, course details discussion, and enrollment completion with documentation support.
Graduates can pursue roles such as Senior Clinical Research Associate, Clinical Project Manager, Regulatory Affairs Specialist, Drug Safety Associate, or Clinical Data Manager. Average salary ranges from ₹6.0 LPA to ₹15.0 LPA depending on experience, role, and organization.
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PG Diploma in Clinical Research Training FAQs
The curriculum includes multi-phase trial simulations, protocol development assignments, regulatory dossier preparation, safety case analysis, and monitoring visit documentation using industry-standard tools like EDC, CTMS, and pharmacovigilance databases.
Students receive mentorship from clinical operations managers and regulatory professionals. Support includes LMS access, live doubt-clearing sessions, project guidance, and peer discussion forums for collaborative learning.
This program integrates IBM-powered tools, AI labs, and live analytics projects far beyond typical theory-based short term healthcare courses, offering tangible experience with industry-grade platforms.
Students get 24×7 access to the Learning Management System containing recorded lectures, protocol templates, ICH-GCP guidelines, regulatory SOPs, case studies, and trial documentation samples for reference and practice.
After completion, students join the Placement Mentorship Program with resume building, mock interviews, LinkedIn profile optimization, and direct referrals to pharmaceutical companies, CROs, and research organizations for senior-level clinical research, regulatory affairs, and drug safety positions.