IQVIA Hiring Senior Clinical Data Coder Job across India. Apply for global clinical data management role with leadership opportunities and CRO experience today.
IQVIA is hiring experienced professionals for the role of Senior Clinical Data Coder across multiple Indian locations. This opportunity is ideal for candidates with strong expertise in clinical data management and medical coding who want to work on global clinical trials. If you have experience handling large-scale studies and want to advance into a leadership-oriented role within a global CRO, this position offers strong career growth and international exposure.
Company Overview
IQVIA is a globally recognized healthcare analytics and clinical research organization that supports pharmaceutical, biotechnology, and medical device companies worldwide. Known for its advanced data science capabilities and clinical trial expertise, IQVIA plays a crucial role in accelerating drug development and improving healthcare outcomes. With a strong presence in India, the company offers dynamic roles in clinical data management, pharmacovigilance, and regulatory services.
Job Location & Employment Type
- Locations:
- Bangalore
- Thane (Maharashtra)
- Kolkata
- Kochi
- Employment Type: Full-time
- Industry: Clinical Research / CRO
Open Positions / Department Details
- Job Title: Senior Clinical Data Coder
- Department: Clinical Data Management (CDM)
- Seniority Level: Mid-Senior / Leadership Track
This role involves leading coding activities within clinical trials and supporting project delivery across multiple global studies.
Key Roles & Responsibilities
The Senior Clinical Data Coder will act as a subject matter expert in clinical coding and data management. Core responsibilities include:
- Managing single and multi-service clinical data projects while ensuring quality deliverables within defined timelines and budgets.
- Acting as a key contact for internal stakeholders and external clients for coding-related deliverables.
- Leading coding operations for large global clinical studies and providing mentorship to coding teams.
- Serving as a Lead Data Coder or Coding Reviewer for assigned projects.
- Performing comprehensive quality control and validation of coded clinical data.
- Conducting Serious Adverse Event (SAE) reconciliation and supporting pharmacovigilance workflows.
- Managing project planning, milestone tracking, and resource allocation.
- Building and maintaining strong relationships with sponsors and client stakeholders.
- Supporting negotiation discussions related to timelines, budgets, and scope changes.
- Identifying and resolving coding and data quality issues proactively.
- Mentoring junior coders and driving capability development within the team.
- Implementing best practices in coding standards and CDM processes.
- Supporting process improvement initiatives using quality frameworks such as Lean and Six Sigma.
- Contributing to SOP development and work instruction updates.
- Adopting and implementing new technologies to improve data management workflows.
- Representing the organization in industry forums or scientific discussions when required.
This position requires a combination of scientific knowledge, project leadership, and client-facing experience.
Eligibility Criteria
Education
- High School Diploma or equivalent minimum requirement
- Preferred educational background in:
- Pharmacy
- Medicine
- Dentistry
- Nursing
- Life Sciences or related disciplines
Experience
- Around 7 years of relevant experience in clinical trials or clinical data management
- Proven experience managing coding activities for global clinical studies
- Exposure to customer negotiations, bid defenses, or project leadership is preferred
Skills Required
- Strong knowledge of medical dictionaries such as MedDRA, WHO-DD, and ICD classifications
- In-depth understanding of medical terminology, pharmacology, anatomy, and physiology
- Advanced knowledge of clinical data management systems and workflows
- Excellent understanding of the clinical drug development lifecycle
- Strong leadership and mentoring abilities
- Effective project management and milestone tracking skills
- Excellent written and verbal communication in English
- Strong analytical and problem-solving capabilities
- Ability to work independently and make informed decisions
- Client-facing communication and stakeholder management skills
- Knowledge of process improvement methodologies (Lean, Six Sigma) preferred
- High attention to detail and quality-driven mindset
Salary & Benefits
- Compensation: As per company norms
- Additional benefits may include global project exposure, leadership opportunities, health benefits, and professional development programs.
Selection Process
The hiring process may include:
- Online application submission
- Resume shortlisting by talent acquisition team
- Technical and managerial interview rounds
- Final HR discussion and offer release
Only shortlisted candidates will be contacted for further evaluation.
How to Apply
Interested candidates must apply through the official IQVIA careers portal. Ensure that all submitted information is accurate and verifiable, as the company maintains strict hiring integrity standards.
Important Dates
- Application Deadline: March 4, 2026
Candidates are advised to apply early to avoid last-minute application issues.
Why Apply for This Pharma Job?
This role is a strong opportunity for experienced clinical data professionals aiming to move into leadership roles within a global CRO. IQVIA provides exposure to international trials, advanced coding technologies, and cross-functional collaboration with global teams. The position offers opportunities to develop expertise in coding strategy, client engagement, and data governance. Professionals seeking long-term career growth in clinical data management, especially those aspiring to roles like Data Team Lead or CDM Manager, will find this role highly valuable.
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent platform that shares verified pharmaceutical and clinical research job updates for informational purposes only. We are not affiliated with IQVIA or any hiring organization. Candidates should always apply through official company channels and exercise caution while sharing personal information online.
Final Call-to-Action
If you are an experienced clinical data professional looking to take the next step in your career, this Senior Clinical Data Coder opportunity at IQVIA offers global exposure and leadership growth. Apply before the deadline and become part of a world-class clinical research ecosystem.
