Syneos Health Work from Home Clinical Data Associate I Hiring

Are you looking for a remote Clinical Data Management opportunity? Syneos Health, a global leader in biopharmaceutical solutions, is hiring Clinical Data Associate I (Central Lab DM)

to work remotely from India. This is an exciting opportunity for professionals with 1-2 years of Clinical Data Management experience to join a top-tier clinical research organization.

Job Details

 Position: Clinical Data Associate I

Location: Remote (Work from Home – India)

Department: Clinical Data Management (Central Lab DM)

Job ID: 25002203

Job Summary

This role is responsible for supporting all clinical data management activities in complex clinical trials. The candidate will demonstrate high proficiency and offer guidance to other Clinical Data Associates (CDAs), ensuring sample data integrity and timely communication across teams.

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Job Responsibilities

Sample Data Management Responsibilities

• Ensure eCRF informed consent is reconciled before shipment for analysis, as applicable.

• Communicate discrepancies in sample collection data with monitors, sites, and sponsors; resolve issues promptly.

• Coordinate timely communication of sample shipment data to sponsors per study shipping schedule.

• Provide detailed updates on sample data cleaning across assigned studies.

• Review Edit Check documents and Data Transfer Agreements.

• Collaborate with Data Acquisition Specialists on vendor and CRO metadata requirements.

• Perform User Acceptance Testing (UAT) for sample data checks.

• Develop specifications for sample-related edit checks.

• Review and query external data such as PK, PD, Biomarker, and Tissue Samples in real-time.

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General Data Management Responsibilities

• Review Clinical Data Management Plans (CDMPs) and maintain contract awareness.

• Create and input test data for UATs, perform UAT for data entry screens, edit checks, SDV configuration, etc.

• Handle data discrepancies by generating queries or applying permissible global rulings per DMP guidelines.

• Review data validation listings and resolve queries; enter lab normal ranges.

• Complete and manage CDMS-specific access forms or spreadsheets.

• For paper-based studies:

  • Process Data Clarification Forms (DCFs) and CRF database edits.

  • Conduct QC checks and manage document control and filing.

• For EDC studies:

  • Conduct internal QC, perform DM quality reviews, and create electronic storage media.

• Maintain proficiency in DM tools and SOPs via regular trainings (e.g., CDA Knowledge College).

• Conduct SAS mapping QC and document discrepancies.

• Train and coordinate tasks for fellow CDAs.

• Ensure consistency across external datasets (labs, eDiaries, PK, IRT) and the clinical database.

• Perform SAE reconciliation and peer review.

• Generate and review data cleaning and status reports.

• Conduct QC of Data Dictionary and create data cleaning reports and listing specifications.

• Participate in post-migration testing, meetings, and audits.

• Review and provide input on CRFs, database design, and Data Validation Specifications (DVS).

• Serve as backup Project Data Manager (PDM) when required.

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Qualifications

Education & Experience

• Bachelor’s degree in biological sciences, natural sciences, or a related health care field.

• Prior experience in clinical data management or clinical research preferred.

• Familiarity with DM systems such as Oracle Clinical, Medidata Rave, or Inform is advantageous.

Skills & Competencies

• Strong knowledge of clinical data, GCP, and ICH guidelines.

• Proficiency with MS Windows, MS Word, Excel, and Outlook.

• Good understanding of medical terminology.

• Excellent verbal and written communication and interpersonal skills.

• Strong organizational, planning, and time management abilities.

• Able to multitask and work independently or in cross-functional teams.

• Detail-oriented and capable of adapting to shifting priorities.

Other Requirements

• Must comply with company SOPs, business practices, and assigned duties.

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

How to Apply?

Ready to take the next step? Apply now to join Syneos Health’s world-class Clinical Data Management team.

👉 Apply Here

About Syneos Health

With 29,000+ employees across 110 countries, Syneos Health has contributed to 94% of FDA-approved drugs in the last 5 years. Join a company committed to transforming lives through clinical innovation and research excellence.

Quick Job Summary

Company	Syneos Health
Current Openings	Clinical Data Associate I
Required Education	BSc, MSc (Life Sciences, Biotechnology, Microbiology), BPharm, MPharm
Experience Required	1-2 years in Clinical Data Management
Location	Work from Home (India)