Clinical Research Job at IQVIA
Looking for a Clinical Research Job in one of the world’s leading healthcare research organisations? IQVIA Jobs has announced an excellent opportunity for the position of Clinical Data Coder 1 across Bangalore, Thane, Kolkata, and Kochi. If you have qualifications in Life Sciences, Pharmacy, Nursing, Dentistry, or Medicine with experience in clinical data management or medical coding, this Life Science Careers opportunity could be your next career breakthrough. Explore eligibility, responsibilities, locations, and application details below.
About the Company
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. The company supports pharmaceutical, biotechnology, and healthcare organisations through innovative clinical development, real-world evidence, and healthcare intelligence solutions. With operations in over 100 countries, IQVIA offers outstanding Life Science Careers for professionals seeking growth in clinical research, data management, and healthcare innovation.
Job Details:
- Job Title: Clinical Data Coder 1
- Company: IQVIA
- Locations: Bangalore, Thane, Kolkata, Kochi
- Educational Qualification: Degree in Life Sciences or a related field.
Key Responsibilities
- Serve as a Clinical Data Coder, Lead Coder, or Data Operations Coordinator (DOC) for one or more protocols.
- Manage coding activities and standalone coding projects throughout the study lifecycle.
- Validate and test coding applications, coding reports, datasets, edits, and related programming activities.
- Perform clinical data management and coding tasks, including data review and resolution of data clarifications.
- Manage coding project timelines with guidance from the DOC, Data Team Lead (DTL), or Manager.
- Perform Serious Adverse Event (SAE) reconciliation activities.
- Provide backup support for the Lead Coder, DOC, or DTL when required.
- Perform quality control procedures and support the implementation of new technologies.
- Identify and provide coding and project-related solutions to the Data Management team.
- Handle audit requirements for assigned studies and standalone coding projects.
- Follow standard operating procedures and work instructions.
- Perform additional study-related duties as assigned.
- Maintain effective communication and collaboration with team members.
Experience
Minimum 2 years of relevant experience or an equivalent combination of education, training, and experience.
Required Skills
- Excellent knowledge of medical terminology, pharmacology, anatomy, and physiology.
- In-depth knowledge of medical coding dictionaries such as MedDRA and WHODD.
- Understanding of the clinical data management process from study start-up to database lock.
- Knowledge of database technologies related to data management and coding.
- Ability to work independently with strong attention to detail.
- Good understanding of standard operating procedures and work instructions.
- Strong written and verbal communication skills in English.
- Good organisational and leadership skills.
- Ability to build and maintain effective working relationships.
- LPN (Licensed Practical Nurse) State Licensure, where applicable.
