Clinical Data Specialist
Company: Fortrea
Job Location: Bangalore, India
Work Model: Remote
Employment Type: Full-Time
Job Requisition ID: 264324
Application Deadline: August 15, 2026
Job Overview
The Clinical Data Specialist will be a key member of the Clinical Data Management project team, primarily responsible for clinical data review, query generation and resolution, data reconciliation, data listings, and data-quality activities.
The role supports the Data Management Lead in delivering high-quality clinical data according to client specifications, project timelines, GCP requirements, and productivity targets.
The position may also contribute to Data Management Plans, Data Review Guidelines, edit-check specifications, eCRF specifications, database setup, testing, and database lock activities.
Key Responsibilities
Clinical Data Review & Quality
Review clinical trial data according to Data Management Plans (DMPs) and Data Review Guidelines.
Identify erroneous, missing, incomplete, or inconsistent clinical data.
Generate and resolve data queries to address identified issues.
Track queries through resolution and ensure data quality and integrity.
Perform data reconciliation activities.
Run additional programs, special listings, and discrepancy reports to support clinical data review.
Generate and QC data listings for internal data-review activities.
Data Management & Study Support
Support the Data Management Lead in project delivery.
Assist with development of:
Data Management Plans
Data Review Guidelines
Edit Check Specifications
eCRF Specifications
Contribute to the setup, maintenance, and closure of project Data Management activities.
Participate in project meetings and collaborate with project team members.
Assist with data management system setup based on project requirements.
Maintain required Data Management documentation.
Support eTMF maintenance and other administrative Data Management activities.
Database & Edit Check Testing
Review Edit Check Specifications and database specifications.
Create or assist in creating dummy data for testing.
Test edit checks and database screen functionality.
Support testing of SAS reports and data listings.
Identify and communicate issues found during testing.
Reporting & Sponsor Support
Prepare study status reports for Sponsor meetings.
Generate reports and listings based on specific Sponsor requirements.
Support data review and reconciliation reporting.
Maintain accurate project trackers and documentation.
Database Lock & Project Closeout
Assist with Database Lock and Unlock activities.
Support required documentation and quality checks during lock/unlock processes.
Ensure Data Management activities are completed according to project timelines.
Training & Team Collaboration
Support training of new team members on project-specific Data Management processes.
Collaborate effectively with other project team members.
Participate in meetings and provide timely updates.
Demonstrate a constructive problem-solving approach when dealing with deadlines, incomplete information, or unexpected issues.
Compliance & Quality
Ensure project activities are conducted according to:
Clinical trial protocols
Fortrea Global Harmonized SOPs
GCP requirements
Project-specific Data Management Plans
Applicable quality standards
Follow study timelines and meet agreed project deliverables.
Maintain productivity and quality targets.
Escalate data-quality or project issues when required.
Minimum Qualifications
University/College degree in:
Life Sciences
Health Sciences
Information Technology
Related discipline
Allied health professional certification from an accredited institution may also be considered.
Fluent English communication skills, both written and verbal.
Required Experience
3–5 years of relevant Clinical Data Management experience with increasing levels of responsibility.
Experience in one or more therapeutic areas.
Knowledge of clinical data management practices.
Strong understanding of clinical trial data review and query management.
Knowledge of medical terminology is preferred.
Scientific/clinical background is preferred.
Strong time-management skills.
Ability to meet project timelines and productivity metrics.
Strong written and verbal communication skills.
Ability to work effectively within a team environment.
Strong organizational and interpersonal skills.
Ability to collaborate with peers and cross-functional project teams.
Strong problem-solving skills with a deadline-focused approach.
Preferred Qualifications
Familiarity with Fortrea's organizational structure.
Knowledge of Fortrea SOPs and internal processes.
Experience with clinical data management systems and related tools would be advantageous.
Experience with data listings, reconciliation, edit checks, and database testing is beneficial.
Core Skills
Clinical Data Management | Clinical Data Review | Query Management | Query Resolution | Data Reconciliation | Data Quality | DMP | Data Review Guidelines | Edit Checks | eCRF | Database Testing | Data Listings | SAS Reports | Database Lock/Unlock | eTMF | GCP | Clinical Trials | Therapeutic Areas | Medical Terminology | Clinical Research | Sponsor Reporting | Data Management Systems
Experience – 1-Line Summary
3–5 years of Clinical Data Management experience with hands-on exposure to clinical data review, query management, reconciliation, edit checks, data listings, database testing, eTMF, and database lock activities.
Salary Package – Market Estimate
The Fortrea JD does not disclose an official salary range. Based on the Bangalore market for Clinical Data Management professionals with 3–5 years of experience, a reasonable expected package is approximately ₹6–10 LPA CTC, with candidates having strong EDC/CDM, SAS, database, and clinical-trial experience potentially targeting ₹8–12 LPA.
Expected market range: ₹6–10 LPA
Strong/experienced candidate: ₹8–12 LPA
Potential upper range: ₹12+ LPA for highly relevant CDM experience and specialized technical skills.
Note: These figures are market estimates and are not an officially confirmed Fortrea salary range.
Work Environment
Remote / Home-based
Office-based work may also be required depending on business needs.
Flexible working shifts may be required.
Overtime and weekend work may occasionally be required.
Candidate should be comfortable working according to business/project requirements.
Ideal Candidate Profile
The ideal candidate should have 3–5 years of hands-on Clinical Data Management experience with strong exposure to clinical data review, query generation/resolution, reconciliation, edit-check testing, data listings, database testing, eTMF, and database lock/unlock activities.
Candidates with experience in clinical trials, EDC/CDM systems, SAS listings/reports, therapeutic-area knowledge, GCP, and Sponsor-facing project work would be particularly well suited for this role.
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