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IQVIA Hiring for 4 Roles in Clinical Data Management | Apply Now

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B.Pharm, M.Pharm, Pharm.D, Msc, BSc, Lifesciences. B.Tech, M.Tech or related degree

Bangalore, Kochi, and Kolkata.

2–15 years

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IQVIA, a global leader in healthcare analytics and clinical research, is expanding its Clinical Data Management (CDM) team across India. If you’re passionate about clinical data, innovation, and real-world healthcare transformation, this is your chance to join one of the world’s most trusted names in life sciences.

IQVIA is hiring for four exciting positions — Clinical Data Specialist, Clinical Database Validation Specialist, Clinical Database Designer, and Manager – Clinical Data Management — across Bangalore, Kochi, and Kolkata.


🧠 Available Positions at IQVIA

1️⃣ Clinical Data Specialist

📍 Location: Bangalore (Hybrid)
🧾 Experience: 2–5 years

Responsibilities:

  • Manage complete study lifecycle: startup, conduct, and closeout.
  • Ensure data quality through accurate database setup and issue resolution.
  • Collaborate with global teams and maintain compliance with regulatory standards.
  • Lead study activities and client communications effectively.

Qualifications:

  • 2–5 years of core CDM experience.
  • Hands-on expertise with Medidata Rave EDC.
  • Proven record in study execution and delivery.
  • Flexibility to work in shifts and hybrid setup.

2️⃣ Clinical Database Validation Specialist

📍 Location: Kochi / Kolkata (Hybrid)
🧾 Experience: 2–4+ years

Responsibilities:

  • Validate edit checks, components, and SAS listings independently.
  • Create and test eCRFs and database specifications.
  • Collaborate with database designers and study teams to ensure validation accuracy.

Qualifications:

  • 2–4+ years in Clinical Database Validation.
  • Strong knowledge of Rave EDC and database testing.
  • Proficiency in validation documentation and reporting.
  • Willingness to work in shifts for global operations.
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3️⃣ Clinical Database Designer / Sr. Clinical Database Designer

📍 Location: Kochi / Kolkata (Hybrid)
🧾 Experience: 2–10 years

Responsibilities:

  • Design and update eCRFs using CDMS tools.
  • Interpret clinical study protocols and prepare Edit Specification Documents.
  • Build and manage EDC systems to ensure high-quality data collection.

Qualifications:

  • 2–4 years of experience in Clinical Data Management.
  • Expertise in Rave EDC and study startup activities.
  • Strong analytical and design skills with attention to detail.
  • Shift flexibility to support global clinical operations.

4️⃣ Manager – Clinical Data Management

📍 Location: Kochi (Office-based)
🧾 Experience: 12–15 years

Responsibilities:

  • Lead and mentor a team of 10–15+ CDM professionals.
  • Oversee multiple studies ensuring quality, compliance, and efficiency.
  • Deliver impactful reports using analytical and visualization tools.
  • Collaborate across cross-functional teams to drive operational excellence.

Qualifications:

  • 12–15 years in Clinical Data Management.
  • Minimum 3 years of team leadership experience.
  • Strong communication, project management, and presentation skills.
  • Hands-on expertise in clinical data operations and people management.

💼 Benefits of Working at IQVIA

  • Hybrid work flexibility (role-dependent)
  • Exposure to global studies and advanced EDC tools
  • Opportunities for leadership and career growth
  • Collaborative, data-driven, and innovative environment

📨 How to Apply

Interested candidates can send their updated CV to:
📧 babymoni.changmai@iqvia.com

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