IQVIA Hiring for Clinical Data Management professionals in Bangalore, Thane, and Kochi. Apply now for global clinical research opportunities.
Company: IQVIA
Locations: Bangalore, Thane, Kochi (India)
Job Type: Full-time
Experience Required: 0–5 years (Freshers and Experienced)
Educational Qualification: B.Sc, M.Sc, B.Pharm, M.Pharm, Life Sciences, Biotechnology, or related disciplines
Last Date to Apply: November 13, 2025
Job Requisition ID: R1509249
Application Mode: Online
About IQVIA
IQVIA is a global leader in clinical research services, advanced analytics, and technology solutions for the life sciences industry. The company operates in more than 100 countries, supporting pharmaceutical, biotechnology, and healthcare organizations with insights that drive innovation and improve patient outcomes. IQVIA Hiring for Clinical Data Management
IQVIA’s mission is to create intelligent connections between healthcare data, analytics, and technology to accelerate the development of new medical treatments. By combining deep scientific expertise with powerful data-driven tools, IQVIA helps its clients design, execute, and deliver high-quality clinical research programs efficiently and ethically. IQVIA Hiring for Clinical Data Management
Working at IQVIA means being part of a team that values data integrity, scientific precision, and patient safety. The company offers a collaborative environment where professionals can contribute to the global healthcare ecosystem and advance their careers in the rapidly growing clinical research industry. IQVIA Hiring for Clinical Data Management
About the Role: Clinical Data Management
IQVIA is currently inviting applications for the position of Clinical Data Management (CDM) at its offices in Bangalore, Thane, and Kochi.
This role is ideal for professionals who have a background in life sciences, pharmacy, or biotechnology and have a strong interest in data accuracy, clinical research, and regulatory compliance.
As part of the global CDM team, you will play a vital role in managing and validating clinical trial data to ensure accuracy, reliability, and compliance with global standards such as ICH-GCP and FDA regulations. IQVIA Hiring for Clinical Data Management
The Clinical Data Management team ensures that every piece of data collected in a clinical trial is accurate, consistent, and scientifically valid, enabling healthcare companies to make informed decisions that ultimately improve patient outcomes. IQVIA Hiring for Clinical Data Management
Job Overview
The selected candidates will be responsible for providing both basic and advanced data management expertise to ensure high-quality clinical data deliverables. You will work as part of the Clinical Data Management (CDM) team to design, develop, validate, and maintain clinical trial databases. IQVIA Hiring for Clinical Data Management
In this role, you may also take on leadership responsibilities under the supervision of a Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.
Your day-to-day tasks will involve database testing, data cleaning, query management, and documentation review. You’ll collaborate closely with cross-functional teams including biostatistics, clinical operations, and regulatory affairs. IQVIA Hiring for Clinical Data Management
Key Responsibilities
- Provide comprehensive data management support to clinical trial projects across multiple therapeutic areas.
- Act as a Data Operations Coordinator (DOC) for one or more studies with less than 5 operational staff or up to 15 moderately complex laboratory studies.
- Participate in or lead specific data management tasks such as database design, data validation, or coding.
- Support or back up Data Team Leads (DTL) as required.
- Conduct data review and cleaning activities to ensure accuracy and consistency in study databases.
- Write, track, and resolve data clarification forms (DCFs) in collaboration with clinical and site teams.
- Assist in the development, testing, and validation of study databases and edit specifications.
- Perform database audits and ensure that all study data meets IQVIA’s global quality standards.
- Maintain documentation and compliance with IQVIA standard operating procedures (SOPs) and global data standards.
- Work closely with the project team to identify and escalate issues impacting timelines or data quality.
- Ensure data readiness for database lock and statistical analysis.
Required Qualifications
- Bachelor’s Degree in Clinical, Biological, or Mathematical Sciences, Life Sciences, Pharmacy, or related fields.
- Equivalent combination of education, training, and relevant experience will also be considered.
- Exposure to medical terminology and familiarity with clinical research processes is preferred.
Desired Skills and Competencies
- Strong attention to detail and accuracy when reviewing data.
- Excellent organizational and time management skills to handle multiple studies and deadlines.
- Good communication and leadership skills, with the ability to coordinate with cross-functional teams.
- Proficiency in computer applications, particularly MS Excel, MS Word, and clinical data tools such as Medidata Rave or Oracle Clinical (if experienced).
- Analytical mindset and ability to identify inconsistencies or data anomalies.
- Self-motivated, proactive, and capable of working independently.
- Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and clinical trial processes.
Why Join IQVIA?
IQVIA offers a unique opportunity to work on cutting-edge clinical research that impacts millions of lives globally.
As part of IQVIA’s Clinical Data Management team, you will: IQVIA Hiring for Clinical Data Management
- Gain exposure to global pharmaceutical and biotechnology clients.
- Work with state-of-the-art data management tools and technologies.
- Collaborate with a network of professionals from diverse scientific backgrounds.
- Participate in continuous training and development programs to enhance your skills.
- Be part of an organization that promotes career advancement and professional growth.
IQVIA’s work culture emphasizes innovation, collaboration, and scientific excellence, making it an ideal place for professionals who are passionate about healthcare and clinical research. IQVIA Hiring for Clinical Data Management
About Clinical Data Management at IQVIA
The Clinical Data Management (CDM) department at IQVIA is responsible for collecting, cleaning, and managing data from clinical trials.
Accurate and timely data management ensures that the results of a clinical trial are valid and reliable. IQVIA Hiring for Clinical Data Management
CDM teams play a crucial role in ensuring data integrity, minimizing errors, and maintaining compliance with regulatory standards.
Their work supports drug development, regulatory submissions, and post-marketing surveillance activities.
A typical clinical data management process includes:
- Database Design and Setup
- Data Entry and Validation
- Query Management
- Medical Coding
- Data Review and Cleaning
- Database Lock and Submission
By joining IQVIA’s CDM team, you will contribute to each of these stages, gaining hands-on experience in global data management practices. IQVIA Hiring for Clinical Data Management
Eligibility Criteria
- Candidates must hold a bachelor’s or master’s degree in Life Sciences, Pharmacy, Biotechnology, or a related scientific field.
- Freshers with relevant academic exposure or internship experience are encouraged to apply.
- Professionals with 1–3 years of experience in data management, clinical research, or clinical operations will be preferred.
Compensation and Benefits
IQVIA offers a competitive compensation package along with a comprehensive range of employee benefits, including: IQVIA Hiring for Clinical Data Management
- Structured training and mentorship programs.
- Opportunities for internal promotions and role advancement.
- Medical insurance and wellness programs.
- Work-life balance with flexible project-based scheduling.
- Access to global knowledge resources and data management tools.
Work Environment
This is a full-time, on-site role at IQVIA’s offices in Bangalore, Thane, and Kochi.
You will work in a collaborative, fast-paced environment alongside data managers, biostatisticians, and clinical research professionals who share a common goal — ensuring quality and reliability in clinical trial data.
How to Apply
Interested candidates can apply online through the official IQVIA careers portal.
Application Link: https://jobs.iqvia.com
- Visit the link above.
- Search for Job Requisition ID – R1509249 or “Clinical Data Management.”
- Read the job details carefully.
- Click on “Apply Now.”
- Create or log in to your IQVIA account.
- Complete the application form and upload your updated resume.
- Submit your application before November 13, 2025.
Final Thoughts
Joining IQVIA as a Clinical Data Management professional is an exceptional opportunity for individuals passionate about clinical research, data integrity, and patient safety.
Whether you are a fresher looking to start your career or an experienced professional aiming to advance in data management, IQVIA provides the platform, training, and global exposure you need to excel in the clinical research industry. IQVIA Hiring for Clinical Data Management
Apply today and take the first step toward a rewarding career in Clinical Data Management at IQVIA.
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