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Sr Cda/ Cda Iii (Data Acquisition Specialist)

5-7 years
Not Disclosed
10 Nov. 25, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Sr. Clinical Data Associate (CDA III) / Data Acquisition Specialist

Location: Pune, India (Hybrid)
Updated: November 12, 2025
Job ID: 25103264
Company: Syneos Health


About the Role

Syneos Health is seeking an experienced Sr. Clinical Data Associate (CDA III) / Data Acquisition Specialist to support global clinical trials through advanced data acquisition and data management activities. This role requires strong expertise in Non-CRF data handling, external vendor data setup, and clinical database operations. The position involves leading CDAs, ensuring data quality, managing deliverables, and providing functional support to Project Data Managers across multiple studies.

This is a senior-level position focused on operational excellence, regulatory compliance, and streamlined study execution.


Key Responsibilities

Data Management and Study Operations

  • Lead Clinical Data Associates in Non-CRF data collection and data management tasks during study setup, conduct, and closeout.

  • Review and follow Data Management Plans (DMP), update as necessary, and ensure adherence to protocol requirements.

  • Create and execute User Acceptance Testing (UAT) for eCRFs, edit checks, roles, SDV matrices and data review listings.

  • Enter and verify lab normal ranges and maintain CDMS access documentation.

  • Perform discrepancy management, apply self-evident corrections, resolve queries, and ensure timely data cleaning.

Study Oversight and Quality Control

  • Conduct internal QC checks, SAE reconciliations, SAS mapping QC, and post-migration testing.

  • Ensure all CRFs, DCFs, and documentation are maintained according to Data Tracking Guidelines.

  • Review database specifications, annotated CRFs, and data structure documents.

  • Ensure external vendor datasets (central labs, eCOA, ePRO, IRT, sensors, PK data) align with the study database.

Leadership and Collaboration

  • Supervise junior CDAs; provide mentoring, training, and performance feedback.

  • Support Project Data Manager (PDM) activities, including metrics reporting and sponsor updates.

  • Act as the primary point-of-contact for Non-CRF data activities, coordinating with cross-functional teams and external vendors.

  • Lead communication with customer study leads regarding data issues and deliverables.

Documentation and Reporting

  • Create and review study-specific documents including DMPs, DVS, CRF/eCRF completion guidelines, and data transfer agreements.

  • Prepare ad-hoc data cleaning reports and validated listings.

  • Participate in sponsor meetings, audits, inspections, internal reviews, and cross-functional discussions.


Required Experience and Qualifications

Education

  • Bachelor’s degree in Biological Sciences, Life Sciences, Health Sciences, or a related discipline.

Professional Experience

  • 5 to 7 years of hands-on experience in Clinical Data Management within global clinical trials.

  • Demonstrated experience in:

    • External vendor data setup and Non-CRF data management

    • Central lab data processes

    • eCOA, ePRO, patient diary systems

    • Device/sensor data testing

    • Data transfer agreements and external data setup

    • IWRS/IVRS testing and study startup activities

Technical Skills

  • Proficiency in EDC platforms such as Oracle Clinical, Rave, or Inform.

  • Strong understanding of relational database management systems.

  • Knowledge of clinical data standards, ICH-GCP, medical terminology, and regulatory expectations.

  • Advanced MS Word, Excel, and general Windows application skills.

  • Strong keyboard accuracy and speed.

Soft Skills

  • Excellent communication, presentation, and interpersonal skills.

  • Strong analytical skills, organizational efficiency, and time management abilities.

  • Ability to work both independently and in cross-functional teams under tight timelines.

  • Leadership capability with experience mentoring and guiding junior team members.

Additional Requirements

  • Ability to manage multiple priorities and adapt to changing timelines.

  • Participation in audits and client meetings as required.

  • Minimal travel up to 25%.


About Syneos Health

Syneos Health is a fully integrated biopharmaceutical solutions organization supporting clinical development, medical affairs, and commercial activities across 110+ countries. Over the past five years, the company has contributed to 94% of FDA-approved novel drugs and 95% of EMA-authorized products.


Important Notes

This job description outlines core responsibilities but is not exhaustive. Syneos Health may assign additional tasks based on project or operational needs. All activities must comply with applicable SOPs, regulatory guidelines, and corporate policies, including ADA requirements for reasonable accommodations.


Summary

This position plays a critical role in Non-CRF data acquisition and clinical data management for global trials. The Sr. CDA/CDA III will lead key data processes, ensure quality deliverables, manage external vendor data, and contribute to the overall success of clinical operations.