FSP - Sr. CRAs & CRA 1/2 - Ophthalmology

Fortrea; Florida; Remote; USD 110,000 - 145,000; Full time

Job summary

Fortrea is seeking experienced CRAs with ophthalmology monitoring expertise for U.S. assignments. Regional travel with occasional outside travel is expected; Oncology and cardiology experience are a plus. We are recruiting Sr. CRAs as well as CRA1/CRA2 with 1–2 years monitoring experience.

You will monitor sites, ensure protocol compliance, manage data quality, and support training and project coordination. Remote work options may apply in a fast-paced, team-oriented environment.

Qualifications

• Bachelor's degree or equivalent in a related health field.
• 4+ years of clinical monitoring experience for Sr. CRAs.
• Ophthalmology monitoring experience is required.
• 60–70% overnight travel.

Responsibilities

• Monitor clinical sites, perform routine visits, and manage close-out activities.
• Lead site management per project plans and liaise with vendors.
• Ensure informed consent and protocol adherence; protect patient safety.
• Verify data integrity on CRFs and other collection tools; monitor for implausible data.
• Oversee registry management and assist with feasibility work as requested.
• Complete SAE reporting and follow-up with narratives and production of reports.
• Perform CRF review, queries, and data resolution per guidelines.
• Assist training of new staff and co-monitoring.
• Coordinate projects as Local Project Coordinator and be a client contact when assigned.
• Perform additional duties as assigned by management.

Skills

Ophthalmology Experience

Clinical Monitoring

CRA Experience

Education

Bachelor's degree or related allied health certification

Job description

Our FSP team is currently seeking experienced CRAs with Ophthalmology monitoring experience, major hub locations around the US will be considered. Regional travel with occasional outside travel at times. Oncology and cardiology experience also a plus. Seeking Sr. CRA level and CRA 1s and 2s (1-2 years of monitoring).

What You Will Do

You 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 plans
• General On-Site Monitoring
• Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
• Ensure 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 data
• Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
• Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
• Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
• Assist with training of new employees, eg. co-monitoring
• Coordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable) and may act as a local client contact as assigned
• Perform other duties as assigned by management

Requirements

• University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
• 4+ years of Clinical Monitoring experience for Sr. CRAs
• Ophthalmology experience is required
• 60-70% overnight travel

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.

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: $110 - $145K based on title

- Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.