Job summary
Job post source
This job is directly from Fortrea
Job overview
The Clinical Research Associate II at Fortrea focuses on Phase I clinical trials in Florida, ensuring high standards of care and compliance in clinical research.
Responsibilities and impact
The role involves monitoring clinical study sites, managing site activities, ensuring protocol adherence, handling serious adverse event reporting, data review, training new employees, and coordinating local clinical projects.
Compensation and benefits
The position offers a target pay range of $100-115K, comprehensive benefits including medical, dental, vision, life insurance, 401(K), paid time off, employee recognition awards, and access to multiple employee resource groups.
Experience and skills
Candidates need at least 1 year of clinical monitoring experience, preferably with Phase I trials, a relevant degree or certification such as nursing licensure, and must reside in Florida.
Work environment and culture
The work environment is fast-paced, technology-driven, requires strict adherence to protocols, adaptability to changing priorities, and strong teamwork and interpersonal skills.
Company information
Fortrea is a clinical pharmacology company focused on clinical trials and research, emphasizing high standards and participant care.
Job location and travel
The position is remote but requires residency in Florida.
Application process
Applications are accepted on an ongoing basis with information available about EEO and accommodation requests.
Unique job features
The job is distinguished by its focus on Phase I clinical trials, use of electronic data collection, and a dynamic, fast-paced environment requiring precise protocol adherence.
Company overview
Fortrea is a global contract research organization (CRO) that specializes in clinical drug and device development, providing comprehensive services from Phase I through IV clinical trials, regulatory guidance, and patient access solutions. The company, headquartered in Durham, North Carolina, was spun off from Labcorp in July 2023 and now operates as a public company listed on Nasdaq. With over 19,000 employees in more than 90 countries, Fortrea leverages its extensive experience and technology-enabled solutions to advance healthcare and support pharmaceutical and biotechnology companies in bringing new therapies to market.
How to land this job
Position your resume to highlight your Clinical Research Associate experience with a focus on Phase I clinical trials and site monitoring responsibilities, emphasizing your ability to manage study sites and ensure protocol compliance.
Emphasize skills in clinical judgment, emergency response, data integrity, SAE reporting, and experience with electronic data capture systems, as these are critical to the role at Fortrea.
Apply through multiple platforms including Fortrea’s corporate career site, LinkedIn, and reputable clinical research job boards to maximize your visibility for this position.
Connect with current Fortrea Clinical Pharmacology team members or Clinical Research Associates on LinkedIn; use ice breakers such as commenting on recent Fortrea clinical trial advancements or asking about their experience with Phase I studies at Fortrea.
Optimize your resume for ATS by including keywords from the job description such as 'Phase I experience,' 'clinical site monitoring,' 'SAE reporting,' 'protocol compliance,' and 'electronic data capture' to ensure your resume passes automated screenings.
Utilize Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application channels, and find LinkedIn contacts to network with, allowing you to focus your time on interview preparation and skill enhancement.
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