Looking to take your clinical data management career global? IQVIA, one of the world’s top healthcare research organizations, is offering exciting Clinical Data Coordinator roles across Kochi, Kolkata, Thane, Hyderabad, Bangalore, and Pune in a hybrid work model.
Whether you’re a seasoned CDM professional with 2+ years of experience or just starting out in the industry with a year of hands-on exposure—this opportunity could put you on the fast track to global clinical research.
🧬 About IQVIA
IQVIA is a name trusted across more than 100 countries for advanced analytics, clinical trial services, and technology-driven research solutions. It partners with pharmaceutical, biotech, and medical device companies to accelerate health innovations.
By combining big data, AI, and deep scientific expertise, IQVIA enables organizations to bring therapies to market faster and more efficiently.
🧑💻 Job Title: Clinical Data Coordinator
🏢 Hiring Company:
IQVIA India
📍 Locations:
Kochi, Kolkata, Thane, Hyderabad, Bangalore, Pune
(Hybrid Work Available)
💼 Job Type:
Full-time | Clinical Data Management
🔍 Job Openings & Key Criteria
IQVIA is hiring for two levels of Clinical Data Management roles:
1️⃣ Experienced CDM Professionals (2.5+ Years)
🔑 Key Requirements:
- Minimum 2.5 years of relevant industry experience.
- Proven work in Core Clinical Data Management processes.
- Full lifecycle experience – Study Startup, Conduct, and Closeout.
- Strong hands-on experience in Medidata Rave EDC.
- Proficient in UAT, query management, data reconciliation, and database lock procedures.
- Open to shift-based work.
- Must be an immediate joiner or have a notice period of up to 60 days.
2️⃣ Junior CDM Professionals (1+ Years)
🔑 Key Requirements:
- At least 1 year of experience in Clinical Data Management.
- Exposure to end-to-end clinical study activities.
- Hands-on experience with Medidata Rave EDC.
- Ability to work in collaborative hybrid teams.
- Willingness to work in flexible shifts.
📘 Educational Qualifications
You must have one of the following degrees from a recognized institution:
- B.Pharm / M.Pharm
- Pharm.D
- BSc / MSc (Life Sciences or related fields)
🚀 Why Choose IQVIA?
Working with IQVIA isn’t just about collecting data—it’s about making a real impact in the world of healthcare and drug development.
Here’s why this opportunity stands out:
🔹 Global Research Impact
You’ll be part of international clinical studies that advance medical science and improve lives worldwide.
🔹 Learning & Career Growth
IQVIA offers career development pathways into project management, data sciences, and clinical operations.
🔹 Hybrid Flexibility
Enjoy the best of both worlds with a hybrid work model that promotes work-life balance.
🔹 Competitive Salary
Attractive salary packages starting from ₹4 LPA to ₹9 LPA, based on experience and role.
🔹 Exposure to the Best Tools
Get access to Medidata Rave, industry-grade analytics, and robust training on clinical study regulations and Good Clinical Practice (GCP).
🧩 What Makes a Great Candidate?
You’ll thrive in this role if you:
- Love working with clinical trial data and systems.
- Pay close attention to detail and understand data integrity principles.
- Have experience in clinical research organizations (CROs) or pharma-backed studies.
- Can work cross-functionally with medical writers, trial managers, and safety teams.
- Adapt quickly to new technologies and enjoy problem-solving in regulated environments.
🧪 Work Culture & Values at IQVIA
IQVIA champions a culture where innovation meets compassion. Here’s what you can expect:
- Team-based projects focused on outcomes and accountability.
- Diversity & Inclusion programs.
- Opportunities to work on international trials with multi-location collaborators.
- Emphasis on data privacy, compliance, and ethical research practices.
💼 Salary & Benefits
| Benefit | Details |
|---|---|
| 💰 Salary | ₹4 – ₹9 LPA |
| 🧘 Work Model | Hybrid (In-office + Remote) |
| 🏥 Insurance | Health, Dental, and Vision |
| 📚 Learning | Regular upskilling & certification programs |
| 🧑💻 Tools | Medidata Rave, Central Monitoring Systems |
📝 Final Thoughts
Whether you are just getting started or already experienced in CDM, IQVIA offers a powerful career path to expand your role in global clinical research.
With robust training, competitive pay, and international projects, this is your chance to work with purpose—bringing treatments to patients faster through reliable and accurate data.
The clinical trials of tomorrow depend on the data managers of today. Step into that future with IQVIA.
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