₹2.4–3.6 LPA
Clinical research coordinator
Runs day-to-day trial activities at a hospital or site
₹2L₹3.5L₹5.5L
Call Us : +91 888 690 4030Email : info@cliniindia.com
Call Us : +91 888 690 4030Email : info@cliniindia.com
Since 2009Flagship program · 4 months
One program, four career domains. Learn clinical trial management, clinical data management, pharmacovigilance and medical writing from industry faculty — with hands-on PV software, mock interviews and placement support.
4 monthsOnline live
3 days/weekMWF or TTS batches
₹25,000All-inclusive, 2 instalments
LifetimeLMS access
Next batch: date TBC · Seats per batch: TBC
Included with APCRM™
Blockchain-based course certification
Hands-on training on PV software
Access to placement software tool
A counsellor will call you back within one working day.
Free, no obligation. Counsellors call Mon–Sat, 9:30 am–6:30 pm.
Curriculum
About ten topics per module, taught through live classes, case studies and assignments.
01
6 core topics
02
6 core topics
03
6 core topics
04
6 core topics
Module 1 of 4
How a new drug is tested in people — and how trials stay safe, ethical and compliant.
Taught throughLive classes · Case studies · Assignments
Leads toClinical research coordinator · CRA
Module 2 of 4
Capture, clean and lock the data every trial depends on.
Taught throughLive classes · Case studies · Assignments
Leads toClinical data associate
Module 3 of 4
Detect, assess and report drug safety issues once medicines reach patients.
Taught throughLive classes · Case studies · Assignments
Leads toDrug safety associate
Module 4 of 4
Write the documents sponsors, regulators and journals ask for.
Taught throughLive classes · Case studies · Assignments
Leads toMedical writer (associate)
Hands-on training
Theory gets you shortlisted. Practice gets you hired. APCRM™ students process cases on pharmacovigilance software and complete workshops on the systems trial teams use every day.
PV database · case entry
Core workshop
Enter, code and report adverse event cases the way drug safety teams do.
Track sites, visits and milestones in a clinical trial management system.
File and maintain the essential documents of a trial.
Apply each module to real-world scenarios, with feedback.
Rehearse the questions CROs and pharma companies ask.
Eligibility
Graduates and postgraduates from these fields can apply.
Biotechnology, microbiology, biochemistry, nursing and related subjects
Biotechnology or biomedical engineering
Fees & batches
Every class is recorded on the LMS, so you can catch up if you miss one.
Careers
Five entry roles across four job families. Pay shown is the industry-average starting range.*
₹2.4–3.6 LPA
Runs day-to-day trial activities at a hospital or site
₹2L₹3.5L₹5.5L
₹3.5–5 LPA
Monitors sites for protocol and GCP compliance
₹2L₹3.5L₹5.5L
₹2.8–4 LPA
Validates trial data and resolves queries
₹2L₹3.5L₹5.5L
₹3–4.5 LPA
Processes adverse event cases on a PV database
₹2L₹3.5L₹5.5L
₹3.5–5 LPA
Drafts study documents and safety narratives
₹2L₹3.5L₹5.5L
*Salary figures are industry averages, not Clini India outcomes. Ranges to be verified against public benchmarks before publishing.
APCRM™ alumni
Watch video
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FAQ
Four months of live online classes, three days a week, with recorded sessions on the LMS.
Yes. Choose an alternate-day or weekend batch; every class is recorded.
A basic course covers GCP and trial fundamentals. APCRM™ adds data management, pharmacovigilance and medical writing, so you can apply across four job families.
Live classes, lifetime LMS access, study material, PV software practice, mock interviews, certification and placement support.
APCRM™ is Clini India’s own program name and curriculum. The certificate is issued by Clini India and verified on blockchain through CredSure.
No. You get placement support — mock interviews, résumé support and referrals. We do not guarantee a job, interview or internship.
Check your eligibility, pick a batch and ask about instalments — on one free call.
Salary figures are industry averages. Clini India does not guarantee job / interview / internship in any form. Please refer to the placement policy.