Fortrea Hiring – Clinical Data Coordinator I | Bangalore

Fortrea, a global Contract Research Organization (CRO), is hiring for the role of Clinical Data Coordinator I at its Bangalore location. This opportunity is suitable for professionals with 3+ years of experience in Clinical Data Management (CDM) who are looking to grow their career in clinical data coordination and trial data operations.

The role focuses on supporting clinical trial data review, discrepancy management, data quality checks, and coordination with cross‑functional study teams to ensure accurate and timely data delivery. Candidates will work in a structured, compliance‑driven environment aligned with global clinical research standards.

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🏢 About Company

Fortrea is a leading global Contract Research Organization (CRO) that focuses on delivering clinical development solutions for the life sciences industry. The company supports pharmaceutical, biotechnology, and medical device organizations across the entire clinical trial lifecycle, from study design to data delivery.

Fortrea is known for its strong expertise in clinical data management, biostatistics, site monitoring, centralized monitoring, and regulatory-compliant trial execution. With a global presence and experienced teams, Fortrea works on international clinical studies across multiple therapeutic areas.

📊 Job Overview

• Position: Clinical Data Coordinator I
• Department: Clinical Researcj
• Location: Bangalore,India
• Experience: 3+ years
• Qualification: B.Pharm, M.pharm
• Job Type: Full-Time
• Last Date of application: Not provided

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📋 Key Responsibilities – Clinical Data Coordinator I at Fortrea

• Ensure that electronic data received from external vendors includes all required protocol parameters, is in the correct format, and is mapped accurately to the correct patients and database fields.
• Support the Lead Data Manager (LDM) in preparing Data Transfer Agreements (DTA) and Data Transfer Specifications (DTS) for vendor data, when required.
• Review data discrepancies generated from study‑specific edit checks related to external/vendor data and manage queries to resolve data issues.
• Assist the LDM in performing validation checks on electronically transferred data for a selected group of patients to ensure correct data loading.
• Support the review of external data edit checks, external data status reports, and external data listings to confirm data quality and completeness.
• Coordinate with Clinical Trial Managers (CTM) and Clinical Research Associates (CRA) to collect local laboratory normal ranges from study sites.
• Investigate and resolve inconsistencies in laboratory normal ranges, maintain proper documentation, and ensure updates are accurate.
• Enter local lab normal ranges into the database and perform quality control (QC) checks to ensure ranges are correctly linked to patient lab results.
• Support communication with vendors and clients regarding data transfer issues, data discrepancies, and validation concerns, under the guidance of senior team members.
• Perform additional tasks and responsibilities as assigned to support study data management activities.

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🎓 Eligibility Criteria

• You should have a degree from a university or college in Life Sciences, Health Sciences, Information Technology, or a related field.
• A certification in an allied health profession (from a recognized institution) is also acceptable.
• If you don’t fully meet the education requirement, relevant work experience may be considered instead.
• You must be comfortable communicating in English, both spoken and written, as this role involves regular documentation and communication.
• You should have at least 3 years of experience in one of the following areas:
  • Pharmaceutical industry
  • Biotechnology
  • Medical devices or diagnostics
  • Clinical trials or clinical research
• An equivalent combination of education and experience will also be considered, as long as you can successfully perform the role’s responsibilities.

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🧠 Required Skills

• Basic understanding of medical terminology is helpful, but not mandatory.
• Strong organizational and planning skills, with the ability to think clearly and solve problems when issues arise.
• Good spoken and written communication skills, with the ability to interact professionally and confidently with internal teams and sponsors.
• Ability to handle multiple tasks at the same time, even when working under pressure or tight timelines.
• Comfortable using Microsoft Office tools such as Word, Excel, and Outlook.
• Good technical aptitude, with willingness to learn new systems and tools.
• Ability to maintain data confidentiality and handle sensitive information responsibly when working with colleagues at all levels.
• Basic understanding of ICH‑GCP principles and the importance of compliance in clinical trials.

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⭐ Job Role Insight

The Clinical Data Coordinator I role is a key support position in clinical research. In this role, you help ensure that clinical trial data coming from labs and external vendors is accurate, complete, and properly recorded in study databases.

You work closely with Lead Data Managers, clinical teams, and vendors to review data, resolve discrepancies, and maintain high data quality throughout the study. This role also involves handling lab normal ranges, data transfers, quality checks, and documentation, which are critical for regulatory compliance and patient safety.

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🎯 Who Should Apply

• You have 3+ years of experience in clinical trials, data management, lab data handling, or external vendor data.
• You come from a background in Life Sciences, Health Sciences, IT, or an allied health field.
• You enjoy working with clinical data, checking for accuracy, and fixing data issues.
• You are comfortable coordinating with clinical teams, data managers, and vendors.
• You like organized work and can handle multiple tasks without missing details.

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💰 Salary & Work Model Insight

• Salary:The salary for this role is competitive and experience‑based. Final compensation depends on your years of experience, skills, and interview performance, in line with industry standards.
• Work Model: This role follows a hybrid / office‑based model in Bangalore, depending on project needs. You may work both from the office and remotely at times.

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💡 Preparation Tips

• Learn the basics of Clinical Data Management, especially external vendor data and lab data handling.
• Be clear on why data quality, accuracy, and compliance are important in clinical trials.
• Revise ICH‑GCP fundamentals and why they matter in clinical research.
• Understand lab normal ranges, data discrepancies, and simple data validation concepts

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🔗 Application Process

Interested candidates should apply only through the official company career website using the link provided below.

Important Disclaimer

This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official website before applying.

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FAQ – Clinical Data Coordinator I