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Medidata Rave Ctms/Etmf- Life Sciences

6+ years
₹15,00,000 – ₹22,00,000 per annum
10 June 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/ M.Sc/ B.Tech/ M.Tech/ BE/ ME 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

Medidata Rave CTMS/eTMF Consultant – Chennai (Hybrid)

Job Summary

A leading life sciences organization is seeking a Medidata eTMF/CTMS Product Consultant for a hybrid position based in Chennai, Tamil Nadu. This role is ideal for professionals with significant experience in clinical trial technologies, especially Medidata Rave, eTMF, and CTMS platforms. The successful candidate will support the implementation, configuration, and user adoption of Medidata solutions to optimize clinical trial operations and ensure regulatory compliance.

Responsibilities

  • Implement and support Medidata eTMF/CTMS platforms

  • Perform configuration changes as per study requirements

  • Oversee study setup and master data creation

  • Manage user access, roles, and permission hierarchies

  • Conduct data reconciliation and perform data cleanup

  • Develop and manage Visual Analytics dashboards and reports

  • Troubleshoot end-user issues and submit enhancement requests

  • Ensure system and process compliance with regulatory standards such as ICH-GCP

  • Conduct training sessions for users and create detailed training manuals

  • Collaborate with cross-functional teams including Clinical Operations and IT

Required Skills & Qualifications

  • Bachelor’s degree in Life Sciences, IT, or a related discipline

  • Minimum 6 years of relevant IT experience in the life sciences industry

  • Proven experience with Medidata eTMF and CTMS platforms

  • Solid understanding of clinical trial processes and workflows

  • Proficiency in Visual Analytics and system configuration

  • Familiarity with regulatory standards (ICH-GCP, GVP)

  • Strong problem-solving and communication abilities

  • Experience in user access control, system documentation, and end-user support

Perks & Benefits

  • Flexible hybrid working model

  • Opportunity to work with global pharma and biotech leaders

  • Involvement in digital transformation of clinical trial systems

  • Competitive compensation (range not disclosed)

  • Professional development in top-tier clinical and PV software tools

Estimated Salary Range

₹15,00,000 – ₹22,00,000 per annum
(Based on typical compensation for Medidata CTMS/eTMF roles with 6+ years of experience in India)

 

About the Company

Our client is a recognized leader in clinical research IT solutions, offering specialized services in clinical trial system implementation, data management, and regulatory compliance. With expertise in platforms like Medidata, Veeva, and Oracle, they empower life sciences organizations to optimize their R&D and drug safety operations across the globe.

Call to Action

If you're a Medidata expert ready to take the next step in your career, apply now to join a fast-growing, globally recognized life sciences company driving innovation in clinical research systems.