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As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Clinical Data Monitor, who is detail-oriented and organized professional to join our team in supporting critical clinical data management activities. This role involves handling study documentation, ensuring data accuracy, and maintaining compliance with regulatory standards. You will play an integral part in managing project files, performing data entry, and supporting operational tasks throughout the study lifecycle. This is a full-time, office-based position in Dallas, TX. If you join us, you will work with some of the worlds leading pharmaceutical, biotechnology, and medical device companies in a vital stage of clinical development: establishing the safety, tolerability, and pharmacokinetics of a new drug. Many are drawn to their profession because of its direct impact on patient care. If this is your case, you will not miss that working in Phase 1 trials. Whilst allowing you to practice your clinical skills and knowledge, youll be involved with the latest medical technologies and treatments, witnessing their development firsthand. When the drug you work with gets approved, you know youll touch many patients lives around the world. WHAT YOU WILL DO You will utilize your skills, knowledge, and clinical judgement to provide a high standard of clinical research. Other key responsibilities:
Understanding and following project-specific guidelines for scanning, indexing, data entry, tracking, and administrative tasks. Scanning and indexing study-related documents such as CRFs and other essential records. Entering clinical data into databases accurately using source documents and performing quality checks. Assisting with EDC user account activations, deactivations, and modifications under supervision. Supporting decommissioning activities, including QC of PDFs/media, preparing shipment packages, and tracking acknowledgments. Maintaining project files in eTMF/TMF and ensuring compliance with SOPs, GCP, and ICH guidelines. Performing archiving duties for both paper and electronic media and keeping accurate records of all tasks. All other duties as needed or assigned.
YOU NEED TO BRING...
BS degree in Life Science/Pharmacy or equivalent/related discipline is preferred. Fortrea may consider relevant and equivalent experience in lieu of educational requirements. 1-2 years' experience in a research environment or related experience. Strong attention to detail and accuracy. Excellent communication and organizational skills. Ability to work collaboratively with a team. Experience in clinical research or related field is a plus.
Work Environment:
Work is performed in a laboratory and/or a clinical environment with exposure to electrical office equipment. Occasional drives to site locations, occasional domestic travel. Exposure to biological fluids. Personal protective equipment required such as protective eyewear, garments and gloves.
Physical Requirements:
Ability to work in an upright and /or stationary position for 6-8 hours per day. Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists to operate lab equipment. Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. Ability to access and use a variety of computer software developed both in-house and off-the-shelf. Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. Regular and consistent attendance. Varied hours may be required.
The important thing for us is you are comfortable working in an environment that is:
Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue. Changing priorities constantly asking you to prioritize and adapt on the spot. Teamwork and people skills are essential for the study to run smoothly. Technology based. We collect our data directly into an electronic environment.
What do you get? Regular, full-time, or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers) 401(K) Paid time off (PTO) Employee recognition awards Multiple ERG's (employee resource groups)
Learn more about our EEO & Accommodations request here.
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Fortrea
paid time off, 401(k)
Oct 27, 2025