- ISO 9001 certified
- MSME · Govt of India
- Registered with MCA
Clinical Data Associate Track — Medidata Rave + CDASH + SDTM
Built from 684 live Clinical Data Associate JDs. Medidata Rave, CDASH, SDTM — the toolkit IQVIA, Parexel and Syneos hire freshers for.
The 30-second version
In 12 weeks you'll work on real clinical data associate track — medidata rave + cdash + sdtm tasks using Medidata Rave & Oracle Clinical / RDC, ship Take a sample study from CRF design →… and walk out with an ISO-certified internship certificate, partner project letter and performance-based LOR. Companies hiring our learners: IQVIA, Parexel, Syneos.
Avg salary
₹4 – 8 LPA
from real JDs
Last cohort
23/28 shipped capstone
Avg score 84/100
Top employers
IQVIA · Parexel · Syneos · ICON plc
hiring for these roles right now
Overview
What hiring managers actually ask for
Manage, validate and report clinical-trial data using industry-standard CDISC tools.
Top JD skills
CRF design (CDASH) · Edit-check programming · Data cleaning & query management · SAE reconciliation · Database lock
Roles you can apply for
Clinical Data Associate · CDM Programmer · Data Validation Specialist
Avg salary · Demand
₹4 – 8 LPA · High
Sample employers
IQVIA · Parexel · Syneos · ICON plc · TCS Lifesciences · Cognizant
Tools you'll master
Your mentor
Dr. Meera Krishnan
Lead Mentor · ex-IQVIA · 14 yrs in PV / CDM
Built PV teams at two CROs, audited by FDA twice. Trains the cohort directly through W6, then hands off to specialty mentors.
12-week syllabus
Six modules. Every module ships a deliverable.
Each module maps to a specific JD requirement so you can point recruiters to exactly which skill it proves.
Deployment-Ready Outcome
A Deployment-Ready Clinical Data Associate who can read a protocol, annotate a CRF, raise the right queries and walk through a lock checklist on day one.
Every Arzon track is engineered around the same four-pillar formula so recruiters get the only answer that matters: “Yes, they can contribute with minimal training.”
40% · Pillar
Domain Knowledge
Recruiter ask: “Does this candidate know why the work exists?”
- Clinical trial phases I–IV and stakeholders (sponsor, CRO, site)
- GCP, 21 CFR Part 11 and CDISC standards
- Why data integrity drives regulatory approval
- Data lifecycle from first-patient-in to lock
30% · Pillar
Process Training
Recruiter ask: “Can they follow the SOPs from day one?”
- CRF design and annotation against the protocol
- Edit-check specification and UAT
- Query lifecycle — issue, response, closure
- SAE reconciliation between CDM and PV
- Database lock checklist and audit-trail review
20% · Pillar
Tool Exposure
Recruiter ask: “Do they recognise the screens and workflow?”
- Medidata Rave — study build and edit-check screens
- Oracle Clinical / RDC — concepts and navigation
- Veeva CDMS — workflow and user-management views
- CDISC SDTM mapping basics and Define-XML
10% · Pillar
Workplace Readiness
Recruiter ask: “Will they communicate like a teammate?”
- Site communication etiquette for queries
- Status reporting to data manager and biostats
- Cross-functional handover to PV and biostats
- Documentation discipline for inspection-readiness
When you finish, you can say…
I Know
- · ICH-GCP & 21 CFR Part 11
- · CDISC SDTM / CDASH vocabulary
- · Trial-phase responsibilities
I Understand
- · CRF design and query lifecycle
- · SAE reconciliation flow
- · Database lock checklist
I Have Practiced
- · Annotated CRF for an oncology Phase II
- · Cleaning a 200-row dirty dataset
- · Full study lock package
I Have Exposure To
- · Medidata Rave screens
- · Oracle Clinical / Veeva CDMS workflow
- · SDTM mapping & Define-XML
Topics
- Trial phases I–IV
- ICH-GCP
- Roles: sponsor, CRO, site
- 21 CFR Part 11
Deliverable·GCP self-assessment
Satisfies JD skill
ICH-GCP & 21 CFR Part 11 awareness
Outcomes
By the end of week 12 you can…
Concrete, role-aligned skills, not vague promises.
- Apply crf design (cdash) to production-grade tasks
- Use Medidata Rave + Oracle Clinical / RDC the way IQVIA actually uses them
- Ship the capstone: Take a sample study from CRF design → cleaning → SAE recon → mock database lock
- Walk into interviews with a verifiable certificate, project letter & 3 work samples
- Speak the language of Clinical Data Associate JDs fluently
Real projects you'll ship
Design + annotate a CRF for an oncology Phase II protocol
Build edit checks and run UAT on a Medidata-style EDC
Take a sample study from CRF design → cleaning → SAE recon → mock database lock
Decide
You've seen what you'll ship. Lock your seat.
May 2026 cohort starts 15 May 2026. Seat fee ₹1,065. Refundable if we can't match you to a role.
Certification
Three documents, and they're verifiable
Internship Certificate
Issued by Arzon Global (ISO 9001 certified). Verifiable on /verify.
Project Certificate
Signed by the partner whose project you ship. Real signatures, real names.
Performance LOR
Awarded only if you score ≥85% across modules + capstone.
Try it
See your name on the certificate
Type your name and watch the certificate update live. The QR code links to /verify so any recruiter can confirm it's real.
Certificate ID: ARZ-CLI-2026-01918
Arzon Global · Internship Certificate
ISO 9001 · MSME · MCA registered
This is to certify that
Your Name Here
has successfully completed the structured 12-week internship in
Clinical Data Associate Track — Medidata Rave + CDASH + SDTM
Certificate ID
ARZ-CLI-2026-01918
Verified Clinical Data Management Internship Certificate + Project Letter.
FAQs
Quick answers to the usual questions
Is this Clinical Data Associate Track — Medidata Rave + CDASH + SDTM programme suitable for freshers?+
Yes. The first two weeks are foundational, we don't assume prior pharmacy & life sciences experience. By W4 you'll be working on real data.
Do I get a job guarantee?+
No. Anyone promising guaranteed jobs is breaking ASCI guidelines. We guarantee live mentoring, real-data work, a verifiable certificate, and structured interview access with our hiring partners. See /proof for our refund policy.
How are sessions delivered?+
Live cohort calls 3 evenings a week (90 min each), recordings within 12 hours, async Slack with mentor SLA of 1 hour during cohort hours. The browser-based player tracks your progress.
What if I miss a live session?+
Recordings are available the same day. You can mark lessons complete in the player and submit assignments asynchronously. Mentors do weekend office hours for catch-up.
What does the certificate actually say?+
It states you completed the structured 12-week internship in Clinical Data Associate Track — Medidata Rave + CDASH + SDTM, all six modules, the capstone, and met our performance bar. It carries a unique ID + QR code that resolves on /verify. Try the sample on the certificate page.
Can I pay in instalments?+
Yes, 0% EMI through Razorpay (3 / 6 / 9 months). A ₹1,065 refundable deposit locks your seat; the balance is due 3 days before the cohort starts.
Ready when you are
Join the May 2026 cohort of Clinical Data Associate Track — Medidata Rave + CDASH + SDTM
Starts 15 May 2026. Seat fee ₹1,065. Walk out with an ISO-certified internship certificate and a recruiter-ready portfolio.