Clinical Research Associate II, Phase I - California

Fortrea; California; On-site; USD 100,000 - 120,000; Full time

Job summary

Fortrea is seeking a Clinical Research Associate with at least 1 year of clinical monitoring experience, preferably in Phase I, to support California-based trials. The role involves on-site monitoring, regulatory adherence, and coordination with vendors and study staff.

Responsibilities include ensuring proper informed consent, data integrity, and SAE reporting, with 40–50% overnight travel. The environment emphasizes fast-paced, compliant execution and teamwork across sites.

Qualifications

• 1+ year of clinical monitoring experience; Phase I experience preferred.

Responsibilities

• Monitor study sites for protocol compliance and data integrity.
• Manage site activities, perform pre-study and initiation visits, and assist with close-outs.
• Complete SAE reporting, narratives, and follow-up as required.

Skills

Clinical Monitoring

Site Monitoring

Teamwork

Regulatory Compliance

Travel Readiness

Education

University degree in allied health or nursing

Tools

EDC systems

Job description

Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience and reside in California.WHAT YOU WILL DOYou will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.Responsibilities :Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -Responsible for all aspects of site management as prescribed in the project plansGeneral On-Site MonitoringEnsure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the studyEnsure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirementsEnsure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible dataResponsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requestedComplete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEsIndependently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by managementAssist with training of new employees, eg. co-monitoringCoordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assignedPerform other duties as assigned by managementRequirementsUniversity or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)1+ years of Clinical Monitoring experiencePhase I experience40-50% overnight travelThe 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.Work Environment:Work is performed in an office environment with exposure to electrical office equipment.Frequent travel to clients/ site locations with occasional travel both domestic and international.Physical Requirements: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, 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.Target Pay Range: $100 - $120KApplications will be accepted on an ongoing basis.Learn more about our EEO & Accommodations request here .