Job Title: Clinical Data Specialist
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time | Hybrid
Job ID: R1519993
Experience Required: 2–5 Years (Clinical Data Management)
Job Overview
We are seeking a Clinical Data Specialist to support global clinical research programs by delivering high-quality clinical data management solutions. This role involves hands-on data review, database development, testing, and coordination activities to ensure accurate, compliant, and timely clinical trial data. The position also provides opportunities to take on task-level leadership responsibilities under the guidance of senior data management leaders.
Key Responsibilities
Provide clinical data management expertise to support efficient, accurate, and regulatory-compliant data delivery.
Serve as a Data Operations Coordinator (DOC) for:
A single protocol with fewer than five operations staff (excluding Data Entry), or
Fifteen or more easy to moderately complex central laboratory studies.
Take a leadership role in specific CDM activities such as clinical data coding, database testing, or database design for non-programming-intensive systems.
Act as a backup to the Data Operations Coordinator (DOC) or Data Team Lead (DTL) when required.
Conduct clinical data review and manage discrepancies by writing and resolving data clarifications.
Lead or support database audit activities to ensure data quality and inspection readiness.
Develop, test, and maintain clinical databases and edit check specifications.
Perform testing of database programming and system configurations.
Execute clinical data coding using standard medical dictionaries.
Ensure strict compliance with SOPs, work instructions, and internal quality standards.
Meet assigned project objectives while maintaining effective collaboration with cross-functional CDM teams.
Qualifications & Experience
Bachelor’s degree in Clinical Sciences, Biological Sciences, Mathematical Sciences, or a related discipline.
Equivalent combinations of education, training, and relevant experience will be considered.
2–5 years of experience in Clinical Data Management within a CRO, pharmaceutical, or life sciences organization.
Practical exposure to medical terminology and clinical trial data processes.
Strong organizational, analytical, and problem-solving skills with high attention to detail.
Excellent written and verbal communication skills.
Ability to work independently, demonstrate initiative, and manage priorities effectively.
Proven capability to build and maintain effective working relationships with colleagues, managers, and clients.
Proficiency in clinical data management systems and standard office tools.
Why Join This Opportunity
Work on global clinical trials across multiple therapeutic areas.
Hybrid work model supporting flexibility and work-life balance.
Exposure to end-to-end clinical data management activities.
Career growth opportunities within clinical research and data operations leadership tracks.
About IQVIA
IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence. By creating intelligent connections across the healthcare ecosystem, IQVIA accelerates the development and commercialization of innovative medical treatments, helping improve patient outcomes worldwide.
Apply Now
Qualified candidates with clinical data management experience are encouraged to apply through thepharmadaily.com.
SEO & GEO Keywords:
Clinical Data Specialist Jobs Bengaluru, Clinical Data Management Jobs India, CDM Jobs Bangalore, Hybrid Clinical Research Jobs, IQVIA Careers India, Life Sciences Data Management Jobs
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