FSP Sr. Clinical Research Associate II - East Coast - Ophthalmology

Fortrea; Georgia; Remote; USD 125,000 - 142,000; Full time

Job summary

Fortrea is seeking an Ophthalmology Sr. CRA with 4+ years of monitoring experience to support sites along the East Coast of the United States.

You will conduct site monitoring visits, ensure protocol compliance, manage data quality, and respond to urgent safety events in line with regulatory standards.

The role requires oncology experience, 30–50% overnight travel, a relevant degree, and the ability to thrive in a fast-paced, collaborative team setting.

Qualifications

• Bachelor's degree or related allied health field required.
• 5+ years of Clinical Monitoring experience.
• Oncology experience, early phase preferred.
• 30-50% overnight travel required.

Responsibilities

• Responsible for all aspects of 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.
• Site management as prescribed in project plans.
• General on-site monitoring activities.
• Ensure study staff are properly trained to safely enroll patients.
• Verify informed consent procedures and protocol adherence per regulatory requirements.
• Ensure data integrity on CRFs and other data collection tools.
• Manage registry activities and undertake feasibility work as requested.
• Complete SAE reporting and follow-up with narratives.
• CRF review, query generation and resolution per guidelines.
• Assist with training of new staff (e.g., co-monitoring).
• Coordinate clinical projects as Local Project Coordinator or client contact.

Skills

Clinical Monitoring

Quality & Compliance

Teamwork

Education

Bachelor's degree or related allied health

Tools

EDC systems

Job description

Our FSP team is currently seeking Ophthalmology Sr. CRAs with 4+ years of monitoring residing on the East Coast of the US.

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)
• 5+ years of Clinical Monitoring experience
• Oncology experience, early phase preferred
• 30-50% 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: $125 - $142K

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