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Senior Clinical Data Associate

3+ years
Not Disclosed
10 Nov. 25, 2025
Job Description
Job Type: Full Time Hybrid 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 – Fully Remote (India)

Location: Mumbai, Maharashtra, India
Job Type: Full Time
Category: Clinical Research
Company: Trialmed, Early Phase Clinical Solution for PPD (Thermo Fisher Scientific)


About the Role

Trialmed, part of the global PPD® clinical research business of Thermo Fisher Scientific, is seeking a Senior Clinical Data Associate (Sr. CDA) to support high-impact clinical data management projects. This role offers the opportunity to collaborate with global teams, lead complex data processes, and contribute to research programs addressing critical global health challenges.

The Sr. CDA will support data management operations across multiple studies, ensuring data accuracy, compliance, and robust documentation throughout the lifecycle of clinical trials.


Key Responsibilities

  • Support study start-up activities, including database design, data-entry screen testing, and development of Data Validation Manuals.

  • Identify, investigate, and resolve data discrepancies to ensure high-quality data within clinical databases.

  • Generate, track, and manage data queries and clarifications across assigned studies.

  • Review and validate clinical data listings for accuracy, consistency, and protocol compliance.

  • Serve as a subject matter expert for study-specific processes and data management systems.

  • Provide training, mentoring, and direction to junior team members as needed.

  • Contribute to continuous improvement of global data management processes and standard practices.

  • Prepare and deliver project-specific data management status reports for internal teams and sponsors.

  • Perform reconciliations such as Serious Adverse Events (SAE) and vendor data checks.

  • Manage advanced data cleaning tasks following GCP guidelines, SOPs, and project requirements.

  • Independently execute complex assignments requiring strong judgment, initiative, and problem-solving skills.

  • Interact professionally with external stakeholders, demonstrating strong communication and negotiation skills.


Education & Experience Required

  • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Computer Science, or an equivalent academic background.

  • Minimum 3+ years of experience in Clinical Data Management or a related area within clinical research.

  • Experience working with EDC systems such as Medidata Rave or Veeva Vault.

  • Strong understanding of GCP, clinical trial documentation standards, and Data Validation processes.

A combination of education, formal training, and relevant experience will also be considered.


Skills & Competencies

  • Strong attention to detail and excellent analytical abilities.

  • Proficiency with Microsoft Office and interactive data management tools.

  • Excellent written and verbal communication in English.

  • Strong organizational skills with the ability to manage multiple priorities.

  • Ability to work effectively with global teams and cross-functional stakeholders.

  • Fast learner with adaptability to new technologies, including Generative AI tools.

  • Understanding of medical terminology, study protocols, and data management workflows.

  • Ability to maintain confidentiality of clinical and proprietary information.

  • Capability to work independently or collaboratively in remote or hybrid environments.


Work Conditions

  • Standard work schedule: 1:00 PM to 10:00 PM IST.

  • Flexible work options: Remote, Hybrid, or Office-based.

  • Role requires adherence to Good Manufacturing Practices (GMP) and organizational safety standards.


Why Join Trialmed?

By joining Trialmed, you play a critical part in delivering high-quality clinical data that supports global research, advances new therapies, and contributes to a healthier and safer world. If you are committed to quality, innovation, and operational excellence, this role offers long-term career growth within a leading global CRO.

Apply now and accelerate your career in Clinical Data Management.