FSP CRA 2 & Sr. CRA - Ophthalmology - Remote US

Fortrea; Williamstown (NJ); Remote; USD 130,000 - 142,000; Full time

Job summary

Fortrea is seeking an experienced Senior Clinical Research Associate (CRA) with 3+ years of site monitoring expertise in Ophthalmology to join our FSP team. The position supports monitoring activities across major hub locations in California, Texas, and the Southeast and Northeast US, with substantial travel requirements.

You will conduct monitoring visits, ensure regulatory compliance, manage site files, and collaborate with vendors to maintain data integrity and patient safety throughout the

Qualifications

• 3+ years of Clinical Monitoring experience.
• Overnight travel 30-50%.
• Ophthalmology experience required.

Responsibilities

• 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.
• 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.
• Ensure the protection of study patients by verifying informed consent procedures and protocol requirements.
• Ensure the integrity of data submitted on CRFs or other data collection tools.
• Responsible for registry management as prescribed in project plans; undertake feasibility work when requested.
• Complete SAE reporting and follow-up.
• Independently perform CRF review; query generation and resolution.
• Assist with training of new employees; co-monitoring.
• Coordinate designated clinical projects as a Local Project Coordinator and may act as a local client contact.
• Perform other duties as assigned by management.

Skills

Clinical Monitoring

Overnight Travel

Ophthalmology

Education

College degree

Job description

Our FSP team is currently seeking experienced Sr. CRAs with 3+ years of monitoring ! Ophthalmology expertise required. Open to major hub locations in California, Texas, and the South East & North East 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)
• 3+ years of Clinical Monitoring experience
• 30-50+% overnight travel
• Ophthalmology experience

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: $130 - $142K

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