Medical Device & Diagnostics - CRA 2 - US Remote

Fortrea; California (MO); Hybrid; USD 105,000 - 117,000; Full time

Benefits offered by this job

Medical, Dental, Vision, Life Insurance

401(K)

Paid time off (PTO) – Flex Plan

Employee recognition awards

Job summary

Fortrea is looking for an Experienced Device CRA 2 for their Medical Device & Diagnostics team, based in California, Missouri, or other major hub locations across the US. The role involves site monitoring, ensuring protocol adherence, and managing data integrity in clinical trials. Candidates need a degree in a related health profession and 1-3 years of clinical monitoring experience. The position requires 60-70% travel and offers competitive benefits including medical, dental, vision, and a target pay of $105-117K.

Qualifications

• 1-3 years of Clinical Monitoring experience is required.
• Candidates should be comfortable working in fast-paced environments and adapt to changing priorities.

Responsibilities

• Responsible for monitoring clinical sites and management as per project plans.
• Ensure data integrity and patient protection during studies.
• Coordinate clinical projects as a Local Project Coordinator.

Skills

Clinical Monitoring

Teamwork

Ability to adapt to changing priorities

Education

University or college degree in a related health profession

Job description

Job Overview

We are currently seeking Experienced Device CRA 2s to lead and support our Medical Device & Diagnostics team. Open to major hub locations across the US. 60-70% travel, 7-9 DOS per month.

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 monitoring and data review 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 reports, 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, 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)
• 1-3 years of Clinical Monitoring experience
• Open to various hub locations

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 a 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.

What Do You Get?

Benefits

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
• 401(K)
• Paid time off (PTO) – Flex Plan
• Employee recognition awards
• Multiple ERG’s (employee resource groups)
• Target pay range (based on title): $105-117K

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.

Remote applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.