Associate – Regulatory Affairs
CLINCHOICE
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Job Description
 Location: Kochi, India
Job ID: R1510536
Company: IQVIA
Employment Type: Full-time
Application Deadline: November 30, 2025
Job Overview
The Trainee Clinical Data Coordinator will support the collection, entry, and management of clinical trial data using Clinical Data Management Systems (CDMS). This role ensures efficient, accurate, and high-quality data processing to meet project and customer requirements within the clinical research environment.
Key Responsibilities
- Perform data-related roles such as Data Entry Associate, File Room Associate, Scanning Associate, or Indexing Associate as assigned.
- Process, log, and track clinical study documents in accordance with CRF Tracking and Data Entry Guidelines.
- Enter clinical data accurately and in a timely manner.
- Assist in maintaining Data Management Study files and documentation.
- Ensure compliance with Standard Operating Procedures (SOPs) and Working Instructions.
- Contribute to meeting project deliverables and quality standards.
- Develop and maintain effective communication and collaboration within the Clinical Data Management (CDM) team.
Educational Qualification
- Education:
- High School Diploma or equivalent required.
- Equivalent combination of education, training, and experience may be accepted.
- High School Diploma or equivalent required.
- Skills:
- Strong organizational and communication skills.
- Excellent computer proficiency and familiarity with data entry tools.
- High attention to detail and accuracy.
- Ability to work effectively with coworkers, managers, and clients in a team environment.
- Strong organizational and communication skills.
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Location
 Kochi, India
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