Job summary
Job post source
This job is directly from Fortrea
Job overview
The Clinical Research Coordinator at Fortrea is responsible for overseeing the operational conduct of assigned studies, ensuring compliance with regulatory requirements and maintaining participant safety.
Responsibilities and impact
Daily responsibilities include study set-up, coordination of critical events, protocol review, and ensuring client expectations are met while maintaining quality control throughout the study process.
Compensation and benefits
Employees are eligible for comprehensive benefits including medical, dental, vision, life insurance, 401(K), paid time off, and employee recognition awards.
Experience and skills
Candidates should have a university degree in a related field or equivalent experience, along with 3-4 years of experience in a research environment and knowledge of drug development processes and ICH guidelines.
Career development
Fortrea offers opportunities for personal growth and professional development within a collaborative workspace.
Work environment and culture
The company values teamwork, adaptability, and a fast-paced environment focused on quality and technology-based solutions.
Company information
Fortrea is a leading global contract research organization with decades of experience in clinical development across various therapeutic areas, operating in approximately 100 countries.
Team overview
The Clinical Research Coordinator will work closely with Project Managers, Principal Investigators, and operational staff, potentially mentoring junior team members.
Job location and travel
This position is office-based in Dallas, TX.
Application process
Interested candidates should apply through the Fortrea website, ensuring they provide necessary documentation as specified in the job posting.
Unique job features
This role offers the opportunity to work on Phase 1 trials, directly impacting patient care and witnessing the development of new medical technologies.
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 showcase your clinical research experience, emphasizing your operational accountability and ability to adhere to regulatory and protocol requirements, which are crucial for the Clinical Research Coordinator role at Fortrea.
Highlight your skills in study set-up, participant coordination, and protocol review, as these responsibilities are central to the position and demonstrate your readiness to manage complex studies effectively.
Apply through multiple platforms, including Fortrea's corporate site and LinkedIn, to maximize your exposure and increase your chances of landing an interview for this role.
Connect with professionals in Fortrea's clinical research division on LinkedIn to gather insights about the position and the company culture. Ice breakers could include asking about their experience with a specific study or expressing your interest in their recent projects.
Optimize your resume for Applicant Tracking Systems (ATS) by incorporating keywords from the job description, such as 'clinical research,' 'protocol compliance,' and 'participant safety,' to ensure your application passes initial screenings.
Utilize Jennie Johnson's Power Apply feature to streamline your job application process, ensuring that your resume is tailored, your applications are submitted through the right channels, and you are connected with the right people in your network to enhance your job search.
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