Senior Clinical Data Associate (Immediate Joiners)
Location: India – Remote
Job ID: 25104628
Industry: Clinical Research | Clinical Data Management
Employment Type: Full-time
Experience Required: 5+ Years
Updated: Yesterday
Syneos Health®, a globally recognized biopharmaceutical solutions organization, is seeking experienced Senior Clinical Data Associates for immediate joining. This role is ideal for seasoned clinical data management professionals who can independently manage end-to-end data management activities for global clinical trials while leading and mentoring Clinical Data Associates (CDAs).
The Senior Clinical Data Associate will play a key role in study startup, conduct, and closeout activities and may act as a backup to the Project Data Manager (PDM), ensuring high-quality data delivery in compliance with global regulatory standards.
Clinical Data Management & Leadership
Lead and oversee clinical data management activities across global clinical trials.
Supervise, mentor, and review the work of Clinical Data Associates, ensuring quality and compliance.
Act as a subject matter expert (SME) for data management platforms, processes, and study-specific requirements.
Support and back up the Project Data Manager (PDM) for designated study activities, including sponsor interactions.
Study Execution & Quality Control
Review and maintain study-specific Data Management Plans (DMPs), Data Validation Specifications (DVS), CRF/eCRF completion guidelines, and data transfer agreements.
Perform and review User Acceptance Testing (UAT) for databases, edit checks, listings, roles, and SDV configurations.
Manage discrepancy and query resolution, including self-evident corrections, re-queries, and global rulings.
Perform SAE reconciliation, vendor data reconciliation (lab, ECG, PK/PD, IRT/IVRS), and metrics reporting.
Oversee data cleaning activities, database freeze, and database lock.
Cross-Functional Collaboration
Liaise with Clinical Programming, Biostatistics, Clinical Operations, Safety, and external vendors.
Participate in internal, sponsor, and third-party meetings, audits, and inspections.
Provide EDC and project-specific training to internal and external stakeholders.
Documentation & Compliance
Ensure accurate and timely filing of documents in the Data Management Study File (DMSF).
Perform QC reviews of DMSF and TMF during study conduct and after QuickStart® Camp.
Ensure all activities comply with ICH-GCP, SOPs, corporate business practices, and regulatory requirements.
Education
Bachelor’s degree (BA/BS) in Life Sciences, Biological Sciences, Pharmacy, or a related healthcare discipline.
Experience
Minimum 5+ years of hands-on experience in Clinical Data Management.
Proven experience across study startup, conduct, and closeout phases.
Strong client-facing experience, acting as a primary point of contact, with the ability to work independently.
Mandatory Technical Skills
Edit Check and Database UAT
SAE reconciliation
Local and central laboratory data review
Vendor data reconciliation (Lab, ECG, PK/PD, IRT/IVRS)
Metrics and CPT reporting
Database freezing and locking
Strong communication and stakeholder management skills
Preferred / Good-to-Have Skills
Oracle Clinical, Medidata Rave, or Inform EDC systems
Listing UAT and manual/programmed data listing review
DMW (Data Management Workbench), SDQ (Smart Data Query)
Pinnacle 21, post-production changes (PPC)
Coding knowledge and TMF review experience
Additional Competencies
Strong knowledge of ICH-GCP, clinical data standards, and medical terminology.
Excellent organizational, analytical, and time-management skills.
Ability to lead teams, mentor junior staff, and manage multiple priorities under tight timelines.
Proficiency in MS Word, Excel, Windows-based systems, and clinical data platforms.
Work with an organization involved in over 94% of novel FDA-approved drugs and 95% of EMA-authorized products.
Exposure to large-scale, global, high-impact clinical trials.
Strong career development culture with continuous training and leadership opportunities.
Inclusive and diverse global work environment supporting professional growth and flexibility.
Syneos Health is a fully 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.
Minimal travel may be required (up to 25%).
Job responsibilities may evolve based on business needs.
Syneos Health is an equal opportunity employer committed to diversity, inclusion, and accessibility.
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