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Clinical Data Associate Iii (Immediate Joiners)

Syneos Health
Syneos Health
3-5 years
Not Disclosed
10 Jan. 1, 2026
Job Description
Job Type: Full Time 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

Job Title: Clinical Data Associate III – Immediate Joiners
Category: Clinical Data Management (CDM) / Clinical Research
Location: Remote, India
Employment Type: Full-Time
Job ID: 25104627


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating the delivery of therapies and improving patient outcomes worldwide. With a presence in 110 countries and over 29,000 employees, we provide advanced solutions across clinical development, medical affairs, and commercial operations.

Our Clinical Development model places patients and clients at the center of everything we do, driving innovation, efficiency, and excellence in clinical trial execution. We foster an inclusive culture where diverse perspectives and expertise thrive.


Role Overview

We are seeking a Clinical Data Associate III to join our global team for immediate onboarding. This role supports complex clinical trials with high proficiency, providing guidance to other Clinical Data Associates (CDAs) and ensuring data accuracy, integrity, and regulatory compliance across multiple therapeutic areas, including Vaccine and Oncology trials.


Key Responsibilities

  • Execute all clinical data management (CDM) activities for assigned complex trials in accordance with the Clinical Data Management Plan (CDMP).

  • Maintain awareness of project scope, timelines, and contractual requirements, providing status updates to Project Managers and Biometrics Project Managers.

  • Conduct User Acceptance Testing (UAT) for data entry screens, edit checks, and Targeted Source Data Verification (SDV) configurations.

  • Enter, validate, and reconcile lab results, pharmacokinetic (PK/PD) data, ECG, IVRS, and other study datasets.

  • Manage discrepancy resolution, query handling, and data cleaning; perform manual and automated QC checks for EDC and paper-based studies.

  • Participate in database design review, CRF/eCRF design, edit check creation, and SAS mapping QC.

  • Prepare and maintain documentation in the Data Management Study File (DMSF).

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

  • Support Project Data Manager (PDM) in updating Data Management Plans, CRF Completion Guidelines, and Data Transfer Requests.

  • Generate reports, including Discoverer, BOXI, J-Review, and other ad-hoc data listings.

  • Participate in internal/external audits, team meetings, and training sessions.

  • Provide guidance and mentorship to junior CDAs.


Qualifications & Experience

  • Education: BA/BS in Biological Sciences, Life Sciences, or related discipline.

  • Experience: 3–5 years in Clinical Data Management supporting complex trials, preferably in Vaccine and Oncology therapeutic areas.

  • Hands-on experience with Inform EDC, Rave, Oracle Clinical, or similar CDMS.

  • Proven expertise in query management, discrepancy management, SAE reconciliation, lab/vendor reconciliation, PK/PD data handling, and data cleaning.

  • Knowledge of clinical trial processes (Phases II–IV), ICH-GCP guidelines, and regulatory compliance.

  • Familiarity with medical terminology, CRF/eCRF design, and coding processes.

  • Proficiency in MS Office (Word, Excel, PowerPoint), email, and electronic documentation systems.

  • Excellent communication, interpersonal, organizational, and multitasking skills.

  • Ability to work independently and collaboratively in a remote, cross-functional environment.

  • Experience with clinical trial startup, closeout activities, and metrics tracking preferred.


Why Join Syneos Health

  • Work on global clinical trials impacting thousands of patients worldwide.

  • Gain exposure to complex data management workflows across multiple therapeutic areas.

  • Participate in career development programs, mentorship, and peer recognition initiatives.

  • Contribute to high-quality, regulatory-compliant clinical data that supports drug development and patient safety.

  • Join a diverse, inclusive, and collaborative work culture that values innovation and continuous improvement.


Equal Opportunity Employer: Syneos Health is committed to building a diverse and inclusive workplace. Candidates with transferable skills are encouraged to apply. Reasonable accommodations are available to individuals with disabilities during the recruitment process.