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Sr Cda/ Cda Iii (Data Acquisition Specialist)

5-7 years
Not Disclosed
10 Nov. 27, 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 CDA / CDA III (Data Acquisition Specialist) – Pune, India

Location: Pune, India (Hybrid)
Job Type: Full-Time
Updated: November 12, 2025
Job ID: 25103264

Company Overview

Syneos Health® is a global, fully integrated biopharmaceutical solutions organization focused on accelerating clinical development and improving patient outcomes. With over 29,000 employees across 110 countries, we deliver innovative clinical, medical affairs, and commercial solutions, ensuring patients and customers are at the center of everything we do.

Why Join Syneos Health

  • Lead and mentor Clinical Data Associates (CDAs) in a dynamic, global clinical trial environment

  • Work with cross-functional teams including Data Management, Clinical Operations, Biostatistics, and external vendors

  • Gain exposure to multiple data types including Non-CRF, central lab, eCOA, ePRO, IVRS/IWRS, and device data

  • Opportunity to develop subject matter expertise and enhance leadership skills in data acquisition and management

Role Overview

The Sr CDA / CDA III (Data Acquisition Specialist) is responsible for leading Non-CRF data collection and management activities across multiple clinical studies. This role may also serve as a backup for the Project Data Manager (PDM), ensuring high-quality, compliant data delivery for global clinical trials.

Key Responsibilities

  • Lead and mentor CDAs in Non-CRF data collection and quality review activities

  • Perform data entry, discrepancy review, validation, and reconciliation for various datasets (lab, ePRO, IVRS, device data)

  • Conduct User Acceptance Testing (UAT) and post-migration testing for data capture systems

  • Implement and review external vendor data setups and transfer agreements

  • Collaborate with internal and external stakeholders to resolve data issues and ensure accurate, timely delivery

  • Generate study-specific reports including Discoverer, BOXI, and J-Review

  • Perform QC of Data Management Study Files (DMSF) and ensure adherence to SOPs, DMPs, and regulatory guidelines

  • Participate in audits, sponsor meetings, and cross-functional discussions

  • Act as Subject Matter Expert (SME) for Non-CRF data processes

  • Maintain proficiency in clinical data management systems and processes, including SAS mapping QC and edit checks

Qualifications & Requirements

  • BA/BS in biological sciences, pharmacy, or related healthcare/scientific discipline

  • 5–7 years of experience in Clinical Data Management, including Non-CRF and vendor data activities

  • Experience with central lab data, eCOA/ePRO, patient diaries, device testing, IXRS/IWRS, and data transfer agreements

  • Knowledge of DM practices, relational database systems, and EDC platforms (Oracle Clinical, Rave, or Inform preferred)

  • Strong understanding of clinical data, ICH/GCP guidelines, and medical terminology

  • Excellent organizational, communication, and leadership skills with ability to manage multiple priorities

  • Proficiency in MS Word, Excel, and other Microsoft Office applications

  • Ability to work independently and collaboratively within cross-functional teams

  • Minimal travel may be required (up to 25%)

Impact & Contribution

  • Ensure the accuracy and integrity of Non-CRF and external data for global clinical trials

  • Lead data management activities across multiple studies, providing mentorship and training to CDAs

  • Serve as a key point of contact for cross-functional and vendor coordination, ensuring efficient study execution

Syneos Health Highlights

  • Supported 94% of all novel FDA-approved drugs and 95% of EMA-authorized products

  • Managed over 200 clinical studies across 73,000 sites and 675,000+ trial patients

Learn more: syneoshealth.com

How to Apply

Interested candidates are encouraged to apply directly or join our Talent Network to be considered for this and other upcoming opportunities.