Fortrea Is Hiring A Medical Device & Diagnostics Cra 2

Join our team as an Experienced Device CRA 2! This role is perfect for French-speaking professionals with sponsorship to travel into Canada, offering the opportunity to lead our Medical Device & Diagnostics team across major US hubs with extensive travel. ✈️🌎

About the Role

We are currently seeking a dedicated and skilled CRA to utilize clinical judgement, ensure high standards of participant care, and respond effectively to emergency situations within clinical trials.

What You Will Do

You will leverage your expertise to support our clinical research processes, ensuring compliance, data integrity, and participant safety.

Responsibilities

• Site Monitoring & Management: Conduct routine site visits, close-outs, maintain study files, and liaise with vendors.
• Protocol & Study Conduct: Ensure study staff are properly trained and adhere to protocol and regulatory requirements, safeguarding participant protection and data integrity.
• Data & Registry Management: Oversee data accuracy on Case Report Forms (CRFs), monitor for missing or inconsistent data, and manage registries as prescribed.
• SAE Reporting: Complete Serious Adverse Event reports, follow up, and generate necessary documentation.
• Data Review & Query Resolution: Review CRFs independently, generate queries, and resolve issues using Fortrea or client systems.
• Training & Coordination: Assist in training new staff, perform as a Local Project Coordinator when needed, and serve as a local client contact.
• Additional Duties: Perform other responsibilities as assigned by management.

Qualifications

• University/college degree or certification in a related health profession (e.g., nursing licensure)
• 1-3 years of clinical monitoring experience
• Willingness to work across various hub locations, with 60-70% travel expected (7-9 days of service per month)

Work Environment & Skills

Our environment is fast-paced and evolving, requiring adaptability, teamwork, and strong people skills. You will work primarily in an office setting with extensive travel and utilize advanced electronic data collection tools. 🚀

Key Attributes:

• Thrive in a rapid, detail-oriented setting where protocols and timelines are strictly enforced
• Ability to adapt to changing priorities seamlessly
• Excellent communication and collaborative skills
• Comfortable using technology and electronic data systems

Benefits & Compensation

Eligible full-time or part-time employees working 20+ hours/week can enjoy comprehensive benefits:

• Medical, Dental, Vision, Life, STD/LTD coverage
• 401(k) retirement plan
• Paid Time Off (PTO) with a flexible plan
• Recognition awards
• Multiple Employee Resource Groups (ERGs)
• Target Pay Range: $105,000 – $117,000 per year

Work Environment & Physical Requirements

Work Environment

This position involves working in an office setting with exposure to electrical equipment and frequent travel to client and study sites, both domestically and internationally. 🌍✈️

Physical Requirements

• Extended sitting and safe vehicle operation
• Repetitive hand movements for data entry and documentation
• Occasional crouching, stooping, bending, and twisting of the upper body
• Use of various computer software in-house and off-the-shelf
• Light to moderate lifting (up to 20 lbs.), including luggage and laptops
• Consistent attendance with flexible hours as needed

Location & Application Process

This position is remote, with applications accepted on an ongoing basis. 🌐

Learn more about our EEO & Accommodations policies and submit your application today!