FSP Clinical Research Associate 2

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8‑10 days on site per month, a mix of onsite and remote.

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 to ensure study staff have proper materials and instructions to safely enroll patients.
• Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to applicable regulatory requirements.
• Ensure the integrity of data submitted on Case Report Forms (CRFs) or other data collection tools by careful source documentation.
• Monitor data for missing or implausible entries.
• Responsible for all aspects of registry management as prescribed in the project plans.
• Undertake feasibility work when requested.
• Complete Serious Adverse Event (SAE) reporting, produce reports, narratives and follow‑up of SAEs.
• Independently perform CRF review; generate and resolve queries against established data review guidelines on Fortrea or client data‑management systems as assigned.
• Assist with training of new employees, e.g., 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).
• Minimum 2 years of clinical monitoring experience.
• Ability to travel up to 60 % overnight.
• Comfortable working in a fast‑paced environment where protocol deviations are not tolerated and timelines are critical.
• Adaptability to constantly changing priorities.
• Strong teamwork and interpersonal skills.
• Proficiency with technology‑based data collection in electronic environments.

Work Environment

• Office setting with exposure to electrical office equipment.
• Frequent travel to client/site locations, including occasional domestic and international trips.

Physical Requirements

• Ability to sit for extended periods and operate a vehicle safely.
• Repetitive hand movements of both hands with fast, simple, repeated motions of fingers, hands, and wrists.
• Occasional crouching, stooping, frequent bending and twisting of upper body and neck.
• Ability to access and use a variety of computer software (both in‑house and off‑the‑shelf).
• Light to moderate lifting and carrying (including luggage and laptop) with a maximum lift of 15‑20 lb.
• Regular and consistent attendance; varied hours may be required.

Pay

Target pay range: $100‑112 K. Position is remote‑eligible.

Applications are accepted on an ongoing basis.