Fortrea Hiring Clinical Data Specialist in Bangalore – CDM Jobs 2026

Fortrea is inviting applications for the position of Clinical Data Specialist in Bangalore, India. This opportunity is aimed at professionals with 3–5 years of Clinical Data Management (CDM) experience who have hands-on exposure to clinical data review, query management, reconciliation, eCRFs, edit checks, SAS listings, and database lock activities.

The role offers an opportunity to work with clinical research teams and contribute to the quality, accuracy, and integrity of data generated during clinical trials. Candidates with a background in Pharmacy, Life Sciences, Health Sciences, Information Technology, or related disciplines may be considered based on their relevant experience and skills.

Fortrea Clinical Data Specialist – Job Overview

About the Clinical Data Specialist Role

Clinical Data Specialists play an important role in making sure that information collected during a clinical trial is complete, consistent, and suitable for analysis. In this position, you will be involved in different stages of clinical data management, from reviewing incoming trial data and handling discrepancies to supporting database testing, reconciliation, and database lock activities.

You will work closely with Data Management Leads and other clinical project functions. The role requires strong attention to detail because even small inconsistencies in clinical trial data can affect the overall quality of a study.

Key Responsibilities

The selected candidate may be responsible for the following activities:

• Review clinical trial data in accordance with approved Data Management Plans.
• Perform clinical data review and identify discrepancies requiring further investigation.
• Generate, monitor, and resolve clinical data queries.
• Perform reconciliation activities using appropriate listings and data sources.
• Prepare and review special data listings when required for clinical projects.
• Review Edit Check Specifications and Database Specifications.
• Support the development and review of eCRF specifications.
• Assist with preparation and maintenance of Data Management Plans.
• Perform quality checks of clinical data listings and reports.
• Create dummy data for edit check testing and database validation activities.
• Test database functionality and review relevant SAS reports or listings.
• Maintain accurate Clinical Data Management documentation.
• Support eTMF-related documentation and maintenance activities.
• Prepare sponsor status reports and provide project updates when required.
• Support Database Lock and Unlock activities.
• Work collaboratively with cross-functional clinical research teams.
• Assist with onboarding and training of new team members.
• Follow applicable SOPs, protocols, ICH-GCP requirements, and regulatory expectations.

Educational Qualifications

Candidates should have a university degree in a relevant discipline. Suitable educational backgrounds may include:

• B.Pharm
• M.Pharm
• Pharm.D
• B.Sc. in Life Sciences
• M.Sc. in Life Sciences
• Biotechnology
• Microbiology
• Biochemistry
• Clinical Research
• Health Sciences
• Information Technology
• Allied Health Sciences

A relevant degree combined with practical Clinical Data Management experience can be particularly valuable for this position.

Required Experience

This is an experienced-level Clinical Data Management opportunity. Applicants should have approximately 3–5 years of relevant Clinical Data Management experience.

Experience in the following areas can be beneficial:

• Clinical Data Review
• Clinical Data Cleaning
• Query Management
• Clinical Trial Data Validation
• Data Reconciliation
• eCRF Review
• Edit Check Review and Testing
• Database Lock and Unlock
• SAS Listings
• Clinical Trial Database Activities

Skills Required for Fortrea Clinical Data Specialist

The role requires a combination of technical knowledge, clinical research understanding, and strong communication skills. Candidates should be comfortable working with clinical trial data and identifying inconsistencies or missing information.

• Strong understanding of Clinical Data Management principles.
• Excellent written and verbal English communication skills.
• Good knowledge of clinical research terminology and processes.
• Strong analytical and problem-solving ability.
• Good attention to detail and a quality-focused approach.
• Ability to review and interpret clinical data.
• Understanding of ICH-GCP guidelines.
• Ability to manage multiple project activities and timelines.
• Good teamwork and collaboration skills.
• Ability to communicate effectively with project stakeholders.

Preferred Technical Knowledge

Knowledge or practical exposure to the following areas can strengthen your profile for this position:

• Clinical Data Review Guidelines
• Data Management Plans (DMP)
• Database Specifications
• SAS Listings
• Edit Check Testing
• Clinical Trial Reconciliation
• eTMF Documentation
• Sponsor Communication
• Clinical Research Operations
• Clinical Database Testing
• Data Cleaning and Discrepancy Management

Why Consider a Career with Fortrea?

Working in Clinical Data Management at a global clinical research organization can provide exposure to different clinical development programs, sponsors, therapeutic areas, and project teams. For professionals who want to build a long-term career in CDM, an experienced Clinical Data Specialist role can provide opportunities to strengthen both technical and project-management skills.

Depending on the project and business requirements, professionals may gain exposure to:

• Global clinical research projects
• International sponsor teams
• Clinical Data Management processes
• Multiple therapeutic areas
• Cross-functional clinical teams
• Clinical database activities
• Professional development and learning opportunities
• Career progression within clinical research operations

Who Should Apply?

This opportunity is particularly relevant for Clinical Data Management professionals who already have hands-on experience in clinical trial data review and data cleaning activities.

If you have worked with queries, eCRFs, edit checks, reconciliation, SAS listings, database testing, or database lock activities, this position may align well with your existing experience.

How to Prepare for the Application

Before applying, make sure your resume clearly highlights your actual Clinical Data Management experience. Mention specific activities you have handled rather than listing only general responsibilities.

For example, if you have experience with query management, reconciliation, edit check testing, or database lock, include these skills clearly in your resume. Also highlight your experience working with cross-functional teams, sponsors, clinical databases, and relevant CDM documentation.

How to Apply for Fortrea Clinical Data Specialist Job?

Eligible candidates who meet the required experience and qualification criteria can apply through the official Fortrea careers portal.

Important Note

Applicants are advised to carefully review the eligibility requirements and job description on the official Fortrea careers page before submitting their application. Recruitment requirements, job status, and application availability may change according to the company’s hiring process.

Final Thoughts

The Fortrea Clinical Data Specialist opening in Bangalore is a strong opportunity for professionals looking to continue their career in Clinical Data Management. With responsibilities covering data review, query management, reconciliation, database testing, documentation, and database lock activities, the role can provide valuable experience across several important areas of clinical trial data management.

If your background includes 3–5 years of Clinical Data Management experience and you are comfortable working with clinical trial data and CDM processes, consider reviewing the official job requirements and submitting your application through Fortrea’s career portal.