Senior Clinical Data Associate – Clinical Research
Company: Trialmed / Thermo Fisher Scientific
Location: Remote, India
Job Type: Full-Time
Category: Clinical Data Management / Clinical Research
Experience Required: 3+ years
Job Overview
Trialmed, a global site network and early-phase clinical solution for PPD (Thermo Fisher Scientific’s clinical research business), is seeking a Senior Clinical Data Associate (Sr CDA) to support high-impact data management projects. This role ensures data integrity, compliance, and operational excellence across clinical studies, contributing to the accurate assessment of safety and efficacy of investigational products.
The Sr CDA will act as a supporting data manager, provide guidance to junior staff, and drive process improvements while adhering to GCP, SOPs, and global regulatory standards. This is a fully remote position with flexible work arrangements.
Key Responsibilities
Data Management & Oversight
Support study setup including database design, CRF development, and Data Validation Manual creation
Identify, resolve, and update data discrepancies, ensuring accurate data entry in DM systems
Generate, track, and resolve queries; implement CRF designs as required
Review data listings, validation reports, and reconcile Serious Adverse Events (SAEs) and third-party vendor data
Leadership & Collaboration
Serve as subject matter expert for study-specific processes and provide training and guidance to junior staff
Contribute to global process improvement initiatives for data management
Communicate effectively with internal and external stakeholders, including study teams, vendors, and clients
Advanced Responsibilities
Perform advanced data cleaning with high accuracy, ensuring inspection-ready and analysis-ready datasets
Work independently on complex tasks, demonstrating judgment, creativity, and initiative
Produce project-specific status reports for CDM management and clients
Education & Experience
Education:
Bachelor’s degree in Life Sciences, Pharmacy, or a related field
Experience:
Minimum 3+ years in clinical data management or related field
Hands-on experience with EDC systems (Medidata Rave, Veeva Vault) and electronic trial master files (eTMF)
Skills & Competencies
Strong knowledge of GCP, SOPs, clinical trial protocols, and DM processes
Proficiency with Microsoft Office and interactive clinical data systems
Excellent written and verbal communication skills
Analytical, detail-oriented, and capable of problem-solving independently
Ability to mentor junior team members and manage multiple study tasks
Adaptable, culturally aware, and capable of collaborating with global teams
Familiarity with clinical terminology, database validation, and Generative AI tools
Working Conditions
Standard working hours: 1:00 PM – 10:00 PM IST
Flexible work options: office, remote, or hybrid
Why Join
Contribute to global clinical research projects impacting patient safety and efficacy evaluation
Gain exposure to international clinical studies across therapeutic areas
Enhance your career in clinical data management with opportunities for leadership, process improvement, and cross-functional collaboration
Work with a high-performing, remote global team using modern data management technologies
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