PHARMAFull-time
Associate Trainee, Clinical Data Coordinator
KOCHI (IN)HYBRIDPOSTED: 6/29/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Selected candidates will be responsible for supporting Clinical Data Management activities, including:
Perform clinical data entry into Clinical Data Management Systems (CDMS).
Process, scan, index, and manage clinical study documents.
Track Case Report Forms (CRFs) according to study guidelines.
Maintain clinical study files and documentation.
Ensure data accuracy and quality during entry.
Follow Standard Operating Procedures (SOPs) and working instructions.
Meet assigned productivity and quality metrics.
Collaborate effectively with Clinical Data Management teams.
Maintain confidentiality and compliance with regulatory requirements.
REQUIRED VERIFIED SKILLS
Clinical Data Management
Clinical data entry
Document processing
Data accuracy
SOP compliance
COMPENSATION & REWARDS
₹2.8L - 4.0L per annum
The 2.8 LPA salary package is a standard entry-level compensation for clinical data management roles in India, aligning with current market benchmarks for fresh graduates in the life sciences sector.
ORGANIZATION CONTEXT & CULTURE
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.
TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
EXPECTED CAREER ROADMAP
Joining IQVIA offers excellent learning environment, exposure to Clinical Data Management systems, professional training from industry experts, and career growth in Clinical Research.
APPLICATION ADVISORY
Ensure your resume highlights attention to detail and knowledge of clinical research. Emphasize any internships or academic projects related to data management or documentation during the interview process.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.