Clinical Research Associate 2 – Non Oncology

Fortrea

. Provide a high standard of care for participants in clinical trials and respond to emergency situations based on clinical research standards .

Posted 10/8/2026full-timeUnited StatesJuniorMid-Level💰 $100,000 - $112,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Clinical Monitoring, ensuring compliance with clinical research standards and data integrity while managing study sites and participant care. Proficient in handling emergency situations and adapting to changing priorities in a fast-paced environment.

Highest-signal resume keywords

Clinical Monitoring ExperienceInformed Consent ProceduresData Integrity ManagementSerious Adverse Event ReportingUniversity Degree or Nursing Licensure

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementCase Report Form ReviewData Collection ToolsFeasibility AssessmentProtocol Compliance

Soft Skills

TeamworkAdaptabilityPeople Skills

Tools & Technologies

Data Management SystemsElectronic Data Entry Software

Certifications & Qualifications

Nursing Licensure

Industry Keywords

Clinical Research StandardsEmergency SituationsStudy ProtocolMonitoring Source DocumentsProject Plans

About the role

Key responsibilities & impact

Provide a high standard of care for participants in clinical trials and respond to emergency situations based on clinical research standards
Perform routine monitoring and close-out of clinical sites
Maintain study files and conduct pre-study and initiation visits
Liaise with vendors and perform other assigned duties
Manage study sites according to project plans
Ensure study staff receive proper materials and instructions to safely enter patients into the study
Verify informed consent procedures and protocol requirements comply with applicable regulations
Ensure data integrity in Case Report Forms and other data collection tools by monitoring source documents
Monitor data for missing or implausible information
Manage registries according to project plans and undertake feasibility work when requested
Complete Serious Adverse Event reporting, narratives, reports, and follow-up
Perform CRF review and query generation and resolution in Fortrea or client data management systems
Assist with training new employees through activities such as co-monitoring
Coordinate designated clinical projects as a Local Project Coordinator and act as a local client contact when assigned
Perform other duties assigned by management
Travel frequently to client and site locations, including occasional domestic and international travel

Requirements

What you’ll need

University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
2 years of Clinical Monitoring experience
60% overnight travel
Comfortable working in a fast-paced environment where no deviations from the study protocol are allowed
Ability to handle constantly changing priorities and adapt on the spot
Teamwork and people skills
Ability to work in a technology-based environment and enter data electronically
Ability to sit for extended periods and operate a vehicle safely
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists
Occasional crouching and stooping, with frequent bending and twisting of upper body and neck
Ability to access and use a variety of in-house and off-the-shelf computer software
Light to moderate lifting and carrying of objects, luggage, and laptop computer up to 15–20 lbs
Regular and consistent attendance
Varied hours may be required