Clinical Data Coder I – Clinical Data Management
Job ID: R1525524
Location: Bengaluru, India (Hybrid)
Employment Type: Full Time
Industry: Clinical Research / CRO / Life Sciences
Company: IQVIA
Job Overview
ThePharmaDaily.com is featuring an opportunity for a Clinical Data Coder I in Bengaluru with a hybrid working model. This role is ideal for professionals with experience in clinical data management and medical coding who are seeking to advance their careers within a global Clinical Research Organization (CRO).
The Clinical Data Coder I will provide comprehensive data management and coding expertise to support sponsor requirements and ensure high-quality, compliant clinical trial data throughout the study lifecycle. The role may include responsibilities as a Lead Coder, Data Operations Coordinator (DOC), or support large-scale (mega) clinical trials.
Experience Level
Mid-Level
Experience Required:
Minimum 2 years of relevant experience in Clinical Data Management and/or Medical Coding within clinical research, pharmaceutical, or CRO environments.
Key Responsibilities
Clinical Data Coding and Management
Independently serve as a Clinical Data Coder, Lead Coder, or DOC for one or more clinical study protocols.
Manage coding activities across the full clinical trial lifecycle, from study start-up to database lock.
Deliver stand-alone coding projects with minimal supervision.
Medical Dictionary Coding
Perform coding using standardized medical dictionaries such as MedDRA and WHODD.
Validate and test coding applications, reports, datasets, and programming outputs.
Data Review and Query Resolution
Conduct detailed data review and resolve data clarifications.
Perform Serious Adverse Event (SAE) reconciliation activities.
Apply quality control procedures to ensure data accuracy and compliance.
Project and Timeline Management
Manage coding-related timelines under guidance from the Data Team Lead (DTL), DOC, or Manager.
Act as backup for Lead Coder, DOC, or DTL when required.
Compliance and Audit Support
Handle audit requirements for assigned studies and coding projects.
Ensure adherence to SOPs, work instructions, and regulatory standards.
Collaboration and Communication
Maintain effective working relationships with cross-functional teams, sponsors, and internal stakeholders.
Provide proactive coding solutions and contribute to process improvements.
Support implementation of new technologies in data management operations.
Educational Qualifications
Degree in Pharmacy, Dentistry, Medicine, Nursing, Life Sciences, or related healthcare discipline, or equivalent educational qualification.
LPN (Licensed Practical Nurse) with State Licensure may be required, depending on project assignment.
Required Skills and Competencies
Strong knowledge of medical terminology, pharmacology, anatomy, and physiology.
In-depth expertise in medical coding dictionaries (MedDRA, WHODD).
Understanding of end-to-end clinical data management processes.
Knowledge of database technologies related to clinical data management and coding.
Excellent attention to detail and analytical problem-solving skills.
Strong written and verbal communication skills in English.
Ability to work independently and manage multiple projects efficiently.
Organizational and leadership capabilities.
About IQVIA
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The organization supports the development and commercialization of innovative medical treatments to improve patient outcomes and population health worldwide.
IQVIA maintains strict integrity standards in its recruitment process and enforces a zero-tolerance policy toward candidate fraud and misrepresentation.
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