Job summary
Job post source
This job is directly from Fortrea
Job overview
The Ophthalmology CRA II & Sr. CRAs role at Fortrea involves leading and supporting clinical trial monitoring to ensure high standards of care and data integrity in ophthalmology studies across various US locations.
Responsibilities and impact
The job includes monitoring clinical study sites, managing site activities, ensuring protocol adherence, handling adverse event reporting, performing data review, training new employees, and coordinating clinical projects.
Compensation and benefits
The position offers a target pay range of $105-140K, 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 should have a university or college degree or certification in a related health profession, 1-3+ years of clinical monitoring experience, and preferably ophthalmology experience; flexibility to work in various US hub locations is required.
Work environment and culture
The work environment is fast-paced, technology-based, with a strong emphasis on teamwork, adaptability, and strict adherence to study protocols and timelines.
Company information
Fortrea is a company specializing in clinical research outsourcing, providing full-service support for clinical trials with a focus on quality and compliance.
Job location and travel
The role is remote with open hub locations across the US West Coast, Central, and East Coast regions.
Application process
Applications are accepted on an ongoing basis with information on EEO and accommodations provided by the company.
Unique job features
The job features electronic data collection and the opportunity to work in a dynamic, fast-paced clinical research environment with a focus on ophthalmology.
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 monitoring experience, especially any work related to ophthalmology or similar therapeutic areas, emphasizing your ability to manage study sites and ensure protocol compliance.
Focus on demonstrating your skills in site management, data integrity verification, SAE reporting, and your adaptability in fast-paced, technology-driven environments as outlined in the job description.
Apply through multiple channels such as Fortrea’s corporate careers page, LinkedIn job postings, and other reputable clinical research job boards to maximize your application visibility.
Connect with current Fortrea employees in the clinical monitoring or ophthalmology divisions on LinkedIn, initiating conversations by referencing recent company news, asking about team culture, or inquiring about the challenges and expectations for CRAs at Fortrea.
Optimize your resume for ATS by incorporating keywords from the job description like 'clinical monitoring,' 'ophthalmology,' 'site management,' 'SAE reporting,' and 'protocol compliance' to ensure it passes automated screening.
Use Jennie Johnson’s Power Apply feature to automate tailored applications across multiple platforms, identify and reach out to relevant Fortrea contacts on LinkedIn with personalized messages, and optimize your resume for ATS, freeing you to focus on preparing for interviews and networking.
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