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Trainee- Clinical Data Coordinator

Fresher years
2-5 LPA
15 Feb. 27, 2025
Job Description
Job Type: Full Time Education: B.Pharm, M.Pharm, Pharm D., BSc., MSc., Lifesciences graduate Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Opportunity: Trainee - Clinical Data Coordinator (CDC) | IQVIA, Kochi

Position: Trainee - Clinical Data Coordinator (CDC)
Location: Kochi, India
Job Type: Full-Time
Company: IQVIA

 

Who Can Apply?

  • Eligibility:

    • Education: Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or a related field.

    • Experience: Freshers are eligible to apply. No prior experience is required.

    • Skills Required:

      • Strong organizational and analytical skills.

      • Excellent communication and computer proficiency.

      • High attention to detail and problem-solving ability.

      • Ability to work independently and in a team environment.

 

Job Overview:

As a Trainee - Clinical Data Coordinator (CDC) at IQVIA, you will be responsible for data management activities to ensure high-quality data processing that aligns with regulatory and quality standards. This role provides a great opportunity to gain hands-on experience in clinical data management (CDM) and develop essential skills in the pharmaceutical and healthcare research industry.

Key Responsibilities:

  • Conduct basic data review to ensure accuracy and compliance.

  • Write and resolve data clarifications under the guidance of the Data Operations Coordinator.

  • Perform quality control procedures for data accuracy.

  • Track and maintain clinical trial data in alignment with regulatory requirements.

  • Escalate any data-related issues to the Data Operations Coordinator or Group Manager.

  • Follow core operating procedures and contribute to the Data Management Plan.

  • Understand and work with basic database structures used in clinical research.

  • Collaborate with the Clinical Data Management (CDM) team to ensure smooth data flow and compliance.

 

Why Join IQVIA?

IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights. By joining our team, you will:
✅ Work with industry experts in clinical data management.
✅ Gain exposure to real-world clinical trials and regulatory processes.
✅ Develop a strong foundation for a career in pharmacovigilance, clinical research, and healthcare analytics.

 

How to Apply?

Interested candidates can submit their applications online via IQVIA Careers.

 

Join IQVIA and be a part of a team that accelerates medical innovation and improves global healthcare outcomes! 🚀