Sr CDA/ CDA III (Data Acquisition Specialist)

Syneos Health; Pune District; Hybrid; INR 1,200,000 - 1,800,000; Full time

Job summary

Syneos Health is seeking a Sr CDA / CDA III (Data Acquisition Specialist) to lead Non-CRF data collection and management across global trials. You will mentor CDAs, perform data entry, discrepancy reviews, and QA, and support project data management as needed.

Responsibilities include UAT testing, vendor data setups, and collaboration with internal teams to ensure accurate, timely study data delivery while adhering to SOPs and regulatory guidelines.

Qualifications

• BA/BS in biological sciences, pharmacy, or related discipline.
• Experience in non-CRF data management and vendor data activities.
• Knowledge of DM practices and EDC platforms (Oracle Clinical, Rave, Inform).

Responsibilities

• Lead Non-CRF data collection and quality review across studies.
• Perform data entry, discrepancy review, validation, and reconciliation.
• Conduct UAT and post-migration testing for data capture systems.
• Collaborate with vendors and stakeholders to resolve data issues.
• Generate study reports and ensure timely, compliant data delivery.

Skills

Non-CRF data collection

Data management

Vendor data activities

UAT testing

Data entry

SAS mapping QC

EDC platforms

Leadership

Education

BA/BS in biological sciences or pharmacy

Tools

Oracle Clinical

Medidata Rave

Inform (regulatory systems)

Job description

Sr CDA / CDA III (Data Acquisition Specialist)

Location: Pune, India (Hybrid)

Job Type: Full-Time

Updated: November 12, 2025

Job ID: hidden_mobile4

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
• 57 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