Fortrea Life Science Clinical Data Specialist Jobs, Apply Online
About Fortrea:
Fortrea is a global contract research organization (CRO) headquartered in Durham, North Carolina, specializing in clinical development and patient access solutions. Spun off from Labcorp in 2023, Fortrea operates in over 90 countries with around 19,000 employees. The company offers end-to-end services across Phase I-IV clinical trials, clinical pharmacology, and post-approval support. With decades of experience, Fortrea has contributed to the development of numerous leading therapies across oncology, neurology, and rare diseases.
Job Description:
We are looking for a Sr Clinical Data Specialist to join our team in a client-dedicated role, supporting complex and innovative oncology studies.
Job Responsibilities:
In this client-facing position, you will take ownership of external data oversight, including data acquisition, integration, review, and reconciliation from various third-party vendors such as central labs, imaging, and eCOA providers. You will ensure external data is delivered in accordance with client quality standards, data integrity requirements, and study timelines. Acting as a key liaison between the client, vendors, and internal stakeholders, you will contribute to the development and execution of study-specific data strategies and play a critical role in ensuring the successful delivery of high-quality data for oncology clinical trials.
Qualifications (Minimum Required):
- University/college degree in life sciences, health sciences, or related fields.
Experience (Minimum Required):
- 1-3 years of experience in Clinical Data Management or working with Clinical Trial protocols.
- Proficiency in the clinical trial process, data management, clinical operations, biometrics, and relevant system applications.
- Strong time management skills with a focus on meeting project productivity metrics and timelines.
- Ability to work collaboratively in a team environment, demonstrating excellent communication and interpersonal skills.
- Solid organizational skills and a good understanding of medical terminology.
- Background in science or related scientific fields.
- Effective oral and written communication abilities in local language and in English.
Preferred Qualifications:
- Two or more years of Electronic Data Capture experience.
If you meet these requirements and are enthusiastic about contributing to a dynamic work environment, we encourage you to apply and be part of our team!
Keywords: Sr Clinical Data Specialist, Clinical Data Management, Clinical Trial Protocols, Data Management
