CDM Job at Fortrea | Apply Now
CDM job opportunities are growing rapidly in the clinical research industry, and Fortrea is currently hiring a Clinical Data Monitor, Phase I – Early Phase Clinical Research in Dallas, Texas. This full-time role offers candidates the chance to work with one of the world’s leading clinical research organizations while contributing to early-phase clinical trials for pharmaceutical, biotechnology, and medical device companies. Professionals looking for fortrea careers, jobs in Texas, and rewarding life sciences job opportunities can explore this exciting opening.
- Job Title: Clinical Data Monitor, Phase I – Early Phase Clinical Research – Dallas, TX
- Location: Dallas
- Time Type: Full time
- Application End Date: May 8, 2026
- Job Requisition ID: 262122
About the Company
CDM job seekers looking for global clinical research opportunities can explore this opening at Fortrea. As one of the largest Clinical Research Organizations worldwide, Fortrea operates Early Phase Clinical Research Units in both the United States and the United Kingdom. The company supports pharmaceutical, biotechnology, and medical device organizations through high-quality clinical research services and innovative trial solutions.
Professionals interested in fortrea careers can gain hands-on exposure to investigational drugs, emerging medical technologies, and early-phase clinical trial operations while working in a fast-paced and technology-driven environment.
CDM Job Description
CDM job responsibilities at FORTREA involve supporting core clinical data management activities while ensuring data accuracy, completeness, and regulatory compliance throughout the study lifecycle. The Clinical Data Monitor plays a critical role in maintaining study documentation, performing data entry, and assisting with operational activities across multiple projects.
This role contributes directly to early-phase clinical trials focused on evaluating the safety and pharmacokinetics of investigational drugs. Candidates pursuing life sciences job opportunities will collaborate with experienced research teams supporting leading pharmaceutical and biotechnology companies.
CDM Job Qualifications
CDM job applicants should meet the following qualifications:
- Bachelor’s degree in Life Sciences, or a related field preferred
- Relevant experience may be considered in place of a degree
- 1–2 years of experience in a research environment or related setting
- Strong attention to detail and accuracy
- Effective communication and organizational skills
- Ability to work collaboratively within a team
- Experience in clinical research is considered an advantage
Candidates searching for life sciences job opportunities with career growth potential may find this role highly valuable.
Work Environment
CDM job work conditions include laboratory and clinical research environments with exposure to electrical office equipment and biological fluids. Personal protective equipment such as gloves, garments, and protective eyewear may be required.
Additional work environment details include:
- Occasional domestic travel and drives to site locations
- Fast-paced clinical research setting
- Strict adherence to study protocols and timelines
- Constantly changing priorities requiring adaptability
- Team-oriented workflow with strong communication needs
- Technology-based data collection systems and electronic environments
Physical Requirements
CDM job candidates should be comfortable with the following physical requirements:
- Ability to remain in an upright and/or stationary position for 6–8 hours daily
- Frequent repetitive hand movements for operating lab equipment and computer systems
- Occasional crouching, stooping, bending, and twisting movements
- Ability to use multiple software systems and computer applications
- Light to moderate lifting and carrying of objects up to 15–20 lbs
- Regular and consistent attendance with varied working hours when required
Employee Benefits
CDM job opportunities at FORTREA offer comprehensive employee benefits for eligible full-time and part-time employees working 20 or more hours weekly, including:
- Medical, Dental, and Vision Insurance
- Life Insurance and STD/LTD coverage
- 401(K) benefits
- Paid Time Off (PTO)
- Employee Recognition Awards
- Employee Resource Groups (ERGs)
Candidates interested in fortrea careers can also gain valuable experience coordinating people, processes, and customer-service-related activities within clinical research operations.
Key Responsibilities
CDM job duties for this role include:
- Follow project guidelines for scanning, indexing, data entry, tracking, and administrative activities
- Scan, index, and manage study documents, including CRFs and essential records
- Enter and verify clinical data with high accuracy
- Assist with EDC account setup, updates, and deactivations
- Support decommissioning activities including PDF/media QC, shipment preparation, and tracking
- Maintain project files in eTMF/TMF according to SOPs, GCP, and ICH requirements
- Perform archiving duties for paper and electronic records
- Complete additional operational tasks as required to support study activities
Professionals exploring jobs in Texas within clinical research can benefit from the practical exposure and operational experience offered in this role.
Why Consider This CDM Job Opportunity?
CDM job openings like this provide an excellent opportunity for candidates interested in clinical data management, early-phase research, and clinical operations. This position allows professionals to build experience in a globally recognized clinical research organization while contributing to innovative drug development and emerging healthcare technologies.
For professionals searching for jobs in Texas, this role combines career growth, practical industry exposure, and the opportunity to work alongside leading pharmaceutical and biotechnology organizations.
