Skills: Protocol design, CRFs, source data verification, GCP compliance, and data integrity across multicenter studies.
Outcomes: Faster study start‑up, cleaner datasets, and audit‑ready documentation that accelerates approvals.
Pharmacovigilance
- Skills: Case intake, triage, MedDRA coding, signal detection, narratives, and regulatory reporting timelines.
- Outcomes: Safer products, compliant submissions, and proactive risk management aligned with global standards.
- Outcomes: Safer products, compliant submissions, and proactive risk management aligned with global standards.
Clinical Data Management
- Skills: EDC builds, edit checks, query management, SDTM mapping, and database lock workflows.
- Outcomes: High‑quality, analysis‑ready data delivered faster with traceable, validated processes.
- Outcomes: High‑quality, analysis‑ready data delivered faster with traceable, validated processes.
Regulatory Affairs
- Scope: Dossier strategy, submissions, labeling, variations, and lifecycle management across global markets.
- Impact: Faster approvals, fewer deficiencies, and sustained compliance with evolving regulatory requirements.
- Impact: Faster approvals, fewer deficiencies, and sustained compliance with evolving regulatory requirements.
About CET
Join CET and take the first step towards with Successful Career
About Us
CLINICAL EDU TECH initiative in India, delivers industry‑ready training focused on Clinical Research, Pharmacovigilance, Clinical Data Management, Regulatory Affairs, and Clinical SAS through practical, project‑based modules aligned to CRO and pharma workflows, led by expert mentors with real‑world experience in trials, safety, data standards, and submissions; flexible live online and classroom formats (weekday/weekend) include structured labs, case studies, audit‑ready documentation, and scalable learning with lifetime access to recordings and materials, supported by curriculum updates aligned to current regulations, MedDRA, CDISC/SDTM, EDC tools, and a technology edge with AI, data analytics, and cloud practices used by leading CROs. Placement support covers interview prep, resume building, referrals, and campus/virtual drives, alongside a comprehensive catalog (Medical Coding, Medical Writing, Aggregate Reporting, and advanced tracks), industry connect via workshops, webinars, and events, pan‑India reach tailored for students, professionals, colleges, and corporates, plus certification‑ready pathways—Best clinical research training in India with placement, pharmacovigilance courses, and clinical data management certification.
..
Growth with CET
Clinical Research Coordinator (CRC)
A Clinical Research Coordinator oversees site-level clinical trial operations, manages participant recruitment and data collection, and ensures compliance while liaising with sponsors and investigators.
Clinical Research Associate (CRA)
A Clinical Research Associate monitors trial sites, verifies data and compliance, and supports investigators to ensure adherence to Good Clinical Practice.
Drug Safety Associate (DSA)
A Drug Safety Associate monitors and reports adverse drug reactions, manages safety databases, and ensures patient well-being through pharmacovigilance.
Regulatory Affairs Specialist
A Regulatory Affairs Specialist manages regulatory submissions, ensures compliance throughout the product lifecycle, and advises teams on strategy while liaising with authorities.
Clinical SAS Programmer
A Clinical SAS Programmer develops and validates SAS code to analyze clinical trial data, produce regulatory outputs, and ensure data accuracy through collaboration with statisticians and data managers.
Join us where curiosity meets purpose—because here, learning isn't just about knowledge, it's about transformation.
Get More
What You’ll Gain
Join our CET— Learn, Lead, Grow and Get into Dream JOB
Step into a place where ambition meets opportunity—your journey begins here, and greatness is just the first milestone
Expert trainers from reputed companies
Learn directly from seasoned professionals who bring real-world experience into every session.
Career counselling sessions with experts
Get personalized guidance from industry veterans to shape your career path with clarity.
Mock Interviews with real-time feedback
Sharpen your interview skills through simulated sessions and actionable insights.
Individualized attention
Receive tailored support that adapts to your learning style and career goals.
Blog & News
Get Update Blog & News
Under Development
ClinicalEduTech.com is under development Your future in clinical research starts here. ClinicalEduTech.com is under development—get ready for expert-led coaching, courses, and insights.
Read more