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.
Gujarat :
Ahmedabad | Ankleshwar | Baroda | Bharuch | Gandhinagar | Gujarat | Halol | Jhagadia | Mehsana | surat | Tarasadi | Vadodara | Vapi |Maharashtra :
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Delhi | India | New Delhi | PAN-India |Assam :
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Siliguri |Illinois :
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Anchorage | Barrow | Bethel | Juneau | Sitka | Wrangell |Massachusetts :
Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
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Netanya | Kfar Saba | Yavne | Tel Aviv | Be'Er Sheva |Remote :
McFarland | Green Way | Springville | Nairobi | Remote - South America (Latin Americal) | French | Melbourne | Remote, USA | Zaragoza | Medan | Lenexa | Switzerland | Remote - Africa | Bountiful | Remote | Castlebar | Leinster | Bishop | Lousiana | Thailand | Regulatory Labeling Manager (NA and LATAM Only) | Hungary | Texas | Riga | Faridabad | Remote - Europe | Belgium | Tulsa | Minnesota | Ireland | Remote - Middle East | Hammond | Manipal | Slovakia | Victoria | Blue Bell | Xzagreb |Republic of Colombia :
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Kyiv |Lima Region :
Lima |France :
Paris | Lyon |South Africa :
Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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