Biotechnology Jobs at Fotrea | Apply Now for the Clinical Data Coordinator Role
Fortrea is inviting applications for the role of Clinical Data Coordinator – I at its Mumbai location. This full-time position offers an exciting opportunity for professionals with a background in life sciences, health sciences, or information technology to contribute to global clinical trials and data management processes. The role focuses on ensuring data integrity, reviewing external vendor data, managing discrepancies, and supporting protocol-driven data workflows. If you are passionate about clinical data management, vendor data review, and regulatory compliance, this role offers a strong platform to build and grow your career.
- Job Posting: Clinical Data Coordinator – I
- Location: Mumbai, India
- Job ID: 254474
About The Company
Fortrea is a global contract research organization (CRO) that spun off from Labcorp in mid-2023, now operating as an independent publicly traded company dedicated to accelerating drug and medical device development. With a team of approximately 19,000 employees and operations in over 90 countries, Fortrea offers comprehensive Phase I–IV clinical trial management, clinical pharmacology, post-approval patient access services, and innovative technology-enabled solutions.
Job Overview
As a Clinical Data Coordinator, you will support Local Data Managers (LDMs) with external vendor data review, ensuring adherence to departmental SOPs, guidelines, and global standards. The role demands high attention to detail to maintain consistency, resolve discrepancies, and ensure compliance with ICH-GCP principles.
Key Responsibilities
- Review electronic vendor data for protocol compliance, correct formatting, and accurate patient mapping.
- Assist in developing Data Transfer Agreements and Specifications for vendor data transfers.
- Perform query management for discrepancies identified through edit checks.
- Validate electronically transmitted data samples for accuracy before loading.
- Review external data, perform edit checks, update listings, and review status reports.
- Collaborate with clinical staff (CTM/CRA) to obtain and verify local laboratory normal ranges.
- Perform data entry and quality checks for lab ranges, ensuring correct patient results mapping.
- Support communication with vendors and clients on data transfer or validation issues.
- Maintain accurate documentation and confidentiality while ensuring data quality.
- Handle additional duties as assigned.
Qualifications
- Education: University/college degree in Life Sciences, Health Sciences, Information Technology, or related field. Equivalent experience may be considered.
- Experience: Minimum 3 years in pharmaceutical, biotechnology, medical device/diagnostics, or clinical trial industries.
- Skills:
- Basic understanding of medical terminology.
- Strong organizational, planning, and critical-thinking skills.
- Excellent communication skills (written & verbal).
- Proficiency in Microsoft Office Suite.
- Ability to multitask and manage shifting priorities.
- Familiarity with ICH-GCP principles.
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Language Requirement: Fluent in English (spoken & written).
Last date to apply: November 30, 2025
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