Syneos Health Hiring for Clinical Data Associate I Role: CDM Jobs 2026

ByPharma Hiring Hub

Syneos Health is recruiting for the role of Clinical Data Associate I (Archival Activity) in Hyderabad, offering a flexible hybrid work model. This role is an excellent opportunity for professionals with 1–2 years of experience in clinical data management, EDC systems, archival processes, and query management.

As a global biopharmaceutical solutions organization, Syneos Health works across clinical development, medical affairs, and commercialization, partnering with major pharma and biotech companies worldwide. With operations in 110+ countries and involvement in a majority of recent FDA and EMA approvals, this position provides exposure to global clinical trials and high‑quality, regulatory‑compliant data management environments.

This is an ideal career move for candidates looking to gain deeper experience in clinical data archival, documentation workflows, audit‑ready data handling, and collaboration within a global clinical operations team.

Syneos health hiring

Job Overview

  • Position: Clinical Data Associate I (Archival Activity)
  • Department: CDM
  • Location: Hyderabad (Hybrid)
  • Experience: 1 to 2 Years
  • Qualification: B.Pharm, M.Pharm,M.Sc
  • Job Type: Full-Time

Key Responsibilities – Clinical Data Associate I (Archival Activity)

  • Perform data management (DM) quality checks and internal QC activities for Electronic Data Capture (EDC) studies, ensuring data accuracy, consistency, and compliance with study requirements.
  • Contribute to archival processes, assist in basic query management, and support QC activities as part of maintaining audit‑ready study documentation. (1–2 years of experience preferred.)
  • Handle essential administrative tasks related to data management, including documentation, coordination, and filing.
  • Demonstrate strong communication skills while working with cross‑functional teams to support ongoing study operations.
  • Assist in tracking overall project progress, maintaining timelines, and issuing periodic status reports to stakeholders.
  • Help complete activities needed for database finalization, ensuring the clinical database and associated project documents are transferred to the sponsor in accordance with standards.
  • Assist in identifying and confirming study milestone achievements as per the project plan.
  • Create electronic storage media for EDC studies in line with standard operating procedures (SOPs), ensuring secure and compliant document handling.
  • Take part in internal meetings and support internal/external audits when required, providing necessary documentation and assistance.
  • Maintain and file all relevant documents in the Data Management Study File (DMSF) to ensure completeness and audit readiness.
  • Support the archival of study documents, ensuring proper organization and long‑term storage.
  • Demonstrate knowledge of important data review milestones such as interim analyses, dry runs, and data cuts, contributing effectively to timeline‑driven activities.

Required Skills & Qualifications

  • Understanding of the clinical trial database lifecycle and associated data processes
  • Clinical Data Management (CDM)
  • Archival and documentation activities
  • Basic query management
  • Working with EDC systems (Electronic Data Capture)
  • Quality control (QC) related to clinical data
  • Strong communication skills (written & verbal)

Why Join Syneos Health?

Over the last five years, Syneos Health has partnered on the development of the vast majority of global regulatory approvals—including 94% of all newly FDA‑approved drugs and 95% of EMA‑authorized products, while contributing to 200+ clinical studies conducted across 73,000 sites and involving more than 675,000 trial participants. This track record reflects Syneos Health’s unmatched expertise and deep involvement in shaping modern clinical research.

At Syneos Health, every team member—regardless of role—is encouraged to take initiative, challenge traditional ways of working, and contribute meaningfully in a fast‑paced, competitive, and constantly evolving environment. It’s a place where innovation, collaboration, and continuous learning come together to drive breakthroughs in clinical development.

If you’re looking to grow your career with a truly global, impact-driven organization, Syneos Health offers the ideal environment to learn, lead, and innovat

How to Apply

Interested candidates should apply only through the official company career website using the link provided below.

Apply Here

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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FAQ – Clinical Data Associate I (Archival Activity)

1. What does a Clinical Data Associate I (Archival Activity) do at Syneos Health?

A CDA I supports clinical data management activities, focusing on archival, EDC quality checks, documentation, query management, and preparing data for final database lock and transfer to the sponsor.

2. What experience is required for this role?

Clinical Data Management (CDM)
Archival activities
Basic query management
EDC systems
Quality control (QC)

3. What educational background is preferred?

B.Pharm / M.Pharm
BSc / MSc (Life Sciences)
Biotechnology or Clinical Research degree
Any equivalent scientific qualification

4. What are the key responsibilities of this role?

Participating in audits and internal meetings
Performing EDC quality checks and internal QC
Supporting archival and document filing in the DMSF
Assisting in database finalization activities
Creating electronic storage media per SOPs
Tracking project progress and preparing status reports

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