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Senior Clinical Data Associate (Sr. Cda)

3+ years
Not Disclosed
10 Nov. 25, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Senior Clinical Data Associate (Sr. CDA)

Location: Remote, India
Job ID: R-01331306
Employment Type: Full-Time
Category: Clinical Research
Work Model: Fully Remote | Standard Work Schedule (Mon–Fri)


About the Role

Trialmed, a global site network and the early-phase clinical solution supporting PPD, the clinical research business of Thermo Fisher Scientific, is hiring a Senior Clinical Data Associate to lead and support clinical data management activities across global research programs. This position is ideal for experienced professionals who are committed to delivering high-quality data, maintaining compliance, and contributing to critical clinical studies that advance global health.


Key Responsibilities

  • Support key study setup activities including database design, testing of data entry screens, and creation of Data Validation Manuals (DVMs).

  • Identify, resolve, and update data discrepancies within the data management system.

  • Generate, track, and resolve data clarifications and queries; contribute to CRF design as needed.

  • Review data listings for consistency, accuracy, and alignment with study protocols.

  • Serve as the subject-matter expert for assigned study-specific processes.

  • Provide training, guidance, and task direction to junior data management staff.

  • Contribute to the continuous improvement of global data management processes.

  • Prepare and deliver project status reports for internal and client-facing teams.

  • Perform Serious Adverse Event (SAE) and vendor data reconciliations.

  • Execute advanced data cleaning activities according to GCP, SOPs, and protocol requirements.

  • Apply sound judgment and analytical skills to resolve complex data issues.

  • Work independently on specialized tasks and support the development of new processes and techniques.

  • Engage with internal and external stakeholders, requiring strong communication, negotiation, and collaboration skills.


Education and Experience Required

  • Bachelor’s degree in life sciences, health sciences, or a related field (or equivalent qualification).

  • Minimum 3+ years of experience in clinical data management or a related discipline.

  • Experience with EDC platforms such as Medidata Rave and Veeva Vault preferred.

  • Equivalent combinations of education, training, and relevant experience may be considered.


Skills and Competencies

  • Strong understanding of clinical data management processes, global SOPs, and regulatory compliance.

  • Excellent attention to detail with strong analytical and numerical capabilities.

  • Proficiency in Microsoft Office and ability to learn new software tools quickly, including Generative AI.

  • Effective written and verbal communication skills with strong command of English.

  • Strong organizational and time-management abilities.

  • Ability to work independently as well as collaboratively with global teams.

  • High level of confidentiality in handling clinical and proprietary data.

  • Strong interpersonal skills, cultural awareness, and customer-focused mindset.

  • Familiarity with medical and clinical trial terminology, study protocols, and data validation workflows.


Working Conditions

  • Standard working hours: 1:00 PM to 10:00 PM IST.

  • Work options include remote, office-based, or hybrid depending on employee preference.

  • Must adhere to all Good Manufacturing Practices (GMP) and safety standards.


Why Join Us

By joining Trialmed, part of the PPD clinical research portfolio of Thermo Fisher Scientific, you contribute to advancing scientific innovation that impacts global health. This role allows you to collaborate with international teams, drive excellence in data management, and play a key role in early-stage clinical research.

Apply today and be part of a mission-driven team committed to creating a healthier, cleaner, and safer world through high-quality clinical research.