enior Clinical Data Associate (Sr. CDA) – Clinical Research
Job ID: R-01331314
Employment Type: Full-Time
Work Mode: Fully Remote
Location: India (Remote)
Shift: Second Shift (1:00 PM – 10:00 PM IST)
Category: Clinical Research / Clinical Data Management
Job Overview
Trialmed, a global site network and early-phase clinical solutions provider for PPD®, the clinical research business of Thermo Fisher Scientific Inc., is seeking an experienced Senior Clinical Data Associate (Sr. CDA) to join its growing clinical research team in India.
This fully remote role offers an opportunity to work on global clinical trials, supporting high-quality data management activities that ensure the safety, efficacy, and regulatory compliance of investigational drugs and medical devices. The ideal candidate will bring strong technical expertise, leadership capability, and a deep understanding of Good Clinical Practice (GCP) and global data management standards.
Key Responsibilities
Support study start-up activities, including database design, UAT testing, CRF review, and Data Validation Manual (DVM) development
Identify, review, resolve, and document data discrepancies and queries within clinical data management systems
Generate, track, and close data clarifications while ensuring data accuracy and consistency
Review and analyze data listings, validation reports, and reconciliation outputs
Perform advanced data cleaning activities in compliance with GCPs, SOPs, and Work Practice Documents (WPDs)
Conduct Serious Adverse Event (SAE) and third-party vendor reconciliations
Serve as a subject matter expert (SME) for study-specific data management processes
Provide guidance, mentoring, and training to junior data management staff
Prepare and deliver project status reports to internal management and external clients
Contribute to the continuous improvement of global data management processes
Independently manage complex assignments, exercising sound judgment and recommending process enhancements
Collaborate effectively with global cross-functional teams, sponsors, and external stakeholders
Required Education & Experience
Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or a related discipline
Minimum 3+ years of hands-on experience in clinical data management or clinical research operations
Equivalent combinations of education, training, and relevant experience may be considered
Technical Skills & Competencies
Strong working knowledge of clinical data management processes, regulatory guidelines, and global SOPs
Proven experience with EDC systems, particularly Medidata Rave and Veeva Vault
Familiarity with eTMF and good documentation practices
Solid understanding of medical and clinical trial terminology, study protocols, and DVMs
Proficiency in Microsoft Office applications with strong numerical and analytical skills
Excellent written and verbal communication skills with professional-level English
Ability to work independently with moderate supervision in a remote, global environment
Strong problem-solving, organizational, and time-management skills
High level of integrity and ability to maintain confidentiality of clinical and proprietary data
Fast learner with adaptability to new systems, processes, and Generative AI-enabled tools
Collaborative mindset with strong interpersonal and cross-cultural communication skills
Working Conditions
Standard working hours: 1:00 PM to 10:00 PM IST
Flexible work arrangements: Remote, Hybrid, or Office-based options available
Adherence to GMP safety standards, GCP, and company compliance policies
About Trialmed & PPD (Thermo Fisher Scientific)
Trialmed is a global site network delivering early-phase clinical trial solutions as part of PPD®, the clinical research division of Thermo Fisher Scientific Inc. Together, they support the development of innovative therapies that address some of the world’s most complex health challenges.
By combining scientific excellence, operational expertise, and cutting-edge technology, Trialmed and PPD help accelerate clinical development and bring life-changing therapies to patients worldwide.
Why Join Us?
Opportunity to work on global, high-impact clinical trials
Fully remote role with flexible work options
Career growth within a leading global CRO ecosystem
Collaborative, innovation-driven clinical research environment
Apply today and become part of a global clinical research team dedicated to making the world healthier, cleaner, and safer through excellence in clinical data management.
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