Fortrea is hiring for the position of Sr Clinical Data Specialist in Bangalore. This is a full-time opportunity for professionals with experience in Clinical Data Management who are interested in supporting clinical research projects and the delivery of high-quality clinical trial data.
The role focuses on clinical data review, query management, data reconciliation, quality control, and identification of data inconsistencies. Depending on project requirements, the position may also involve supporting Data Management Plans, database design, data review guidelines, validation checks, and project timelines.
Candidates with 4–6 years of Clinical Data Management experience and a university or college degree can apply. Experience with Electronic Data Capture (EDC) systems is preferred.
Fortrea Recruitment 2026 – Job Highlights
| Particulars | Details |
|---|---|
| Company | Fortrea |
| Position | Sr Clinical Data Specialist |
| Job Requisition ID | 265129 |
| Location | Bangalore |
| Job Type | Full Time |
| Work Mode | Office and/or Home-Based |
| Experience | 4–6 Years |
| Qualification | University / College Degree |
| Experience Area | Clinical Data Management |
| EDC Experience | Preferred |
| Application Deadline | 30 September 2026 |
About Fortrea
Fortrea is a clinical research organization supporting clinical development and research activities across the life sciences industry.
The Sr Clinical Data Specialist role is part of the project team responsible for clinical data review and data management activities. The position contributes to maintaining data quality and integrity while helping projects meet defined timelines, productivity requirements, and client specifications.
Job Description
The Sr Clinical Data Specialist supports the delivery of clinical trial data by reviewing clinical data, generating and resolving queries, performing reconciliation, and identifying trends or inconsistencies that may require further investigation.
The role can also support the preparation of Data Management Plans, Quality Management Plans, data review guidelines, database design activities, and data validation checks.
For selected projects, the professional may take on additional operational responsibilities as a Lead Data Reviewer, including technical oversight of data management activities.
Sr Clinical Data Specialist
The position requires a strong understanding of clinical data management processes and the ability to work with project teams across different disciplines. The selected candidate will be expected to maintain data quality while working within project timelines, productivity metrics, and agreed specifications.
Eligibility Criteria
Candidates should meet the following requirements:
- University or college degree, preferably in Life Sciences, Health Sciences, Information Technology, or a related subject.
- 4–6 years of experience in Clinical Data Management.
- Relevant work experience combined with education that is equivalent to a bachelor’s degree may be accepted in lieu of a bachelor’s degree.
- Some knowledge of clinical trial processes, clinical operations, biometrics, data management, and system applications supporting clinical research.
- Ability to manage time effectively and meet project timelines and productivity requirements.
- Ability to work collaboratively within a project team.
- Good organizational, communication, and interpersonal skills.
Preferred Qualifications
The following qualifications and experience are preferred:
- Knowledge of medical terminology.
- Scientific knowledge or a scientific educational background.
- Two or more years of Electronic Data Capture (EDC) experience.
- Familiarity with Fortrea’s organizational structure and Standard Operating Procedures (SOPs).
- Good oral and written communication skills.
Skills and Qualifications
Candidates should have strong capabilities in the following areas:
- Clinical Data Management.
- Clinical trial data review.
- Query generation, resolution, and tracking.
- Data reconciliation.
- Clinical data quality control.
- Data review and discrepancy management.
- Understanding of Data Management Plans.
- Knowledge of data management tools, systems, and processes.
- Ability to identify missing, erroneous, incomplete, or implausible data.
- Aggregate data review at patient, site, and project levels.
- Strong attention to detail.
- Time management and organizational skills.
- Effective written and verbal communication.
- Teamwork and cross-functional collaboration.
Key Responsibilities
The Sr Clinical Data Specialist may be responsible for:
- Reviewing clinical trial data according to applicable Data Management Plans and standardized procedures.
- Identifying erroneous, missing, incomplete, or implausible clinical data.
- Running diagnostic programs, special listings, and reconciliation discrepancy reports to support data review.
- Generating, resolving, and tracking queries related to identified data issues.
- Performing aggregate reviews at patient, site, and project levels.
- Identifying data trends related to patient safety, compliance, and other areas requiring investigation.
- Conducting quality control checks to ensure required data quality standards are achieved.
- Reviewing project documents such as protocols, CRFs/eCRFs, eDiary materials, and related data management documentation when assigned.
- Supporting the development of Data Management Plans and Quality Management Plans.
- Assisting with database design reviews.
- Annotating CRFs/eCRFs according to project specifications.
- Supporting the creation and maintenance of data review guidelines.
- Ensuring data review processes remain consistent with clinical data models and applicable CRF/eCRF conventions.
- Assisting with the development and testing of edit checks, data validation checks, diagnostics, and special listings.
- Supporting Lead Data Managers or Lead Data Reviewers with project timeline development.
- Communicating with project leads and cross-functional team members to support contracted milestones.
- Ensuring service and quality requirements are delivered according to the Data Management Plan and agreed scope of work.
- Informing the Lead Data Reviewer about potential budget overages and supporting the Change Order Log process where applicable.
- Performing quality control of data management activities and study documentation.
- Supporting client or internal audits and helping resolve identified issues within appropriate timelines.
- Addressing client comments with the relevant study team.
- Mentoring or coaching project staff on project-specific and standardized data management processes.
- Performing other related responsibilities assigned by management.
Work Location and Work Environment
The position is based in Bangalore and is listed as a full-time role.
The job posting specifies an office and/or home-based work environment, providing flexibility depending on the applicable work arrangement.
Salary / CTC
The salary or CTC for the Sr Clinical Data Specialist position has not been specified in the provided job posting. Candidates should refer to official Fortrea recruitment communication for compensation-related details.
Selection Process
The detailed selection process has not been provided in the vacancy information. Candidates who meet the eligibility requirements can apply online through the official Fortrea careers portal and follow further instructions from the recruitment team.
How to Apply for Fortrea Recruitment 2026
Interested and eligible candidates can submit their application online through the official Fortrea careers portal.
Position: Sr Clinical Data Specialist
Job Requisition ID: 265129
Location: Bangalore
Job Type: Full Time
Application Deadline: 30 September 2026
Candidates should review the complete job requirements before submitting their application and ensure that all information provided is accurate.
Important Details Before Applying
- Company: Fortrea
- Position: Sr Clinical Data Specialist
- Requisition ID: 265129
- Location: Bangalore
- Job Type: Full Time
- Work Environment: Office and/or Home-Based
- Experience: 4–6 Years
- Qualification: University / College Degree
- Primary Experience: Clinical Data Management
- EDC Experience: 2+ years preferred
- Application Deadline: 30 September 2026
- Application Mode: Online
Important Note
Candidates should carefully verify their qualifications and Clinical Data Management experience before applying. Vacancy status, deadlines, eligibility requirements, and recruitment conditions may change. Applicants are advised to check the latest information on the official Fortrea careers portal before submitting an application.
FAQs – Fortrea Recruitment 2026
1. What position is Fortrea hiring for?
Fortrea is hiring for the position of Sr Clinical Data Specialist.
2. Where is this Fortrea job located?
The position is based in Bangalore.
3. What qualification is required?
A university or college degree is required, preferably in Life Sciences, Health Sciences, Information Technology, or a related subject. Relevant education and work experience equivalent to a bachelor’s degree may also be considered.
4. How much experience is required?
Candidates should have 4–6 years of Clinical Data Management experience.
5. Is EDC experience required?
EDC experience is listed as a preferred qualification, with two or more years of Electronic Data Capture experience preferred.
6. What are the main responsibilities of a Sr Clinical Data Specialist?
The role includes clinical data review, query generation and resolution, reconciliation, quality control, data trend analysis, support for Data Management Plans, validation checks, audit support, and collaboration with clinical research project teams.
7. Can the job be performed from home?
The job posting specifies an office and/or home-based work environment.
This version keeps the experience, qualification, EDC preference, work arrangement, responsibilities, and deadline aligned with the supplied Fortrea posting.