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Clinical Data Associate Iii (Immediate Joiners)

Syneos Health
Syneos Health
3-5 years
preferred by company
10 Jan. 8, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Clinical Data Associate III (Immediate Joiners)
Location: India – Remote
Job ID: 25104627
Industry: Clinical Research | Clinical Data Management
Employment Type: Full-time
Experience Required: 3–5 Years
Updated On: January 5, 2026


Job Overview

Syneos Health®, a global biopharmaceutical solutions organization, is hiring Clinical Data Associate III professionals for immediate joining. This role is critical to managing end-to-end clinical data management activities for complex global clinical trials while mentoring junior team members and supporting project data managers.

The ideal candidate will have strong hands-on experience across study conduct and closeout phases, deep expertise in EDC systems, and the ability to work independently in a remote, fast-paced clinical research environment.


Key Responsibilities

Clinical Data Management & Study Execution

  • Execute clinical data management activities for complex clinical trials in compliance with study-specific Data Management Plans (DMPs), SOPs, and regulatory guidelines.

  • Perform User Acceptance Testing (UAT) for EDC systems, including screens, edit checks, listings, roles, and SDV configurations.

  • Review discrepancy outputs, manage queries, apply self-evident corrections, and resolve data issues as per Data Validation Specifications (DVS).

  • Conduct SAE, lab, PK/PD, ECG, IVRS/IRT, and vendor reconciliations.

  • Run data cleaning, quality review, and status reports to ensure data accuracy and integrity.

Quality Control & Compliance

  • Perform internal QC checks, peer reviews, SAS mapping QC, and post-migration testing.

  • Review and maintain CRF/eCRF designs, annotated CRFs, completion guidelines, and data dictionaries.

  • Ensure proper filing of documentation in the Data Management Study File (DMSF).

  • Participate in internal, sponsor, and third-party audits and meetings.

Leadership & Collaboration

  • Coordinate and guide Clinical Data Associates assigned to the project.

  • Provide project-specific and system training to CDAs.

  • Act as Project Data Manager (PDM) backup for selected activities, including sponsor interactions.

  • Collaborate closely with cross-functional teams including Biostatistics, Clinical Programming, Safety, Medical Writing, and Coding teams.


Required Qualifications

Education

  • Bachelor’s degree (BA/BS) in Life Sciences, Biological Sciences, Pharmacy, or a related healthcare discipline.

Experience

  • 3–5 years of hands-on experience in Clinical Data Management.

  • Strong experience in study conduct and closeout phases.

  • Proven expertise with EDC systems such as Inform, Oracle Clinical, and Medidata Rave.

Technical & Functional Skills

  • Proficiency in query management, discrepancy management, data cleaning, and manual data review.

  • Knowledge of database lock, casebook freeze, site closure, and interim/dry run data cuts.

  • Experience with vaccine and oncology therapeutic areas preferred.

  • Familiarity with ICH-GCP guidelines, medical terminology, and coding processes.

  • Working knowledge of CPT/Metrics is an advantage.

Soft Skills

  • Strong written and verbal communication skills.

  • Excellent organizational, time management, and multitasking abilities.

  • Ability to work independently in a remote setup while meeting tight timelines.

Tools & Systems

  • Proficiency in MS Word, Excel, Windows-based systems, and clinical data platforms.


Why Join Syneos Health

  • Work with a global organization involved in over 94% of novel FDA-approved drugs.

  • Exposure to large-scale global trials across multiple therapeutic areas.

  • Career development through structured training, mentorship, and progression opportunities.

  • Inclusive, people-first culture with a strong focus on professional growth and work-life balance.


Additional Information

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

  • Responsibilities listed are not exhaustive and may evolve based on business needs.

  • Syneos Health is an equal opportunity employer committed to diversity, inclusion, and compliance with global employment regulations.


About Syneos Health
Syneos Health is a leading integrated biopharmaceutical solutions organization operating across 110+ countries with over 29,000 professionals worldwide. The company partners with innovators to accelerate the development and commercialization of life-changing therapies.