Clinical Research Associate

2 days ago


Maidenhead, Windsor and Maidenhead, United Kingdom Fortrea Full time
Company Overview: Fortrea is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. Our mission is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need.

We are actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our commitment is to diversity and inclusion in the workforce, and we do not tolerate harassment or discrimination of any kind.

We make employment decisions based on the needs of our business and the qualifications of the individual. We strive for excellence in all aspects of our work and welcome talented individuals to join our team.

Job Description: As a Clinical Research Associate at Fortrea, you will play a crucial role in the success of our clinical trials. Your primary responsibilities will include site management, data integrity, and regulatory compliance. You will ensure that all clinical trial procedures are conducted in accordance with ICH GCP Guidelines and applicable local regulations.

You will also be responsible for monitoring study sites, conducting source document review, and generating queries as needed. Additionally, you will participate in project team meetings, investigator meetings, and teleconferences.

Your expertise will help us deliver high-quality clinical trials, and your contributions will have a direct impact on bringing new treatments to patients worldwide.

Required Skills and Qualifications: To succeed in this role, you will require a university degree or certification in a related allied health profession. You must have a thorough understanding of ICH GCP Guidelines and local regulatory requirements.

A minimum of 2 years of clinical monitoring experience is required, with the ability to monitor study sites independently according to monitoring plans, project requirements, SOPs, and ICH GCP guidelines. You must be able to work with minimal supervision and have good planning, organization, and problem-solving abilities.

Benefits: As a member of our team, you will enjoy a competitive salary of $80,000 - $100,000 per year, depending on experience. You will also receive comprehensive benefits, including medical, dental, and vision insurance, as well as paid time off and holidays.

Our company values diversity and inclusion, and we offer equal opportunities to all candidates regardless of race, religion, color, national origin, gender, sexual orientation, age, veteran status, disability, or genetic information.

Estimated Salary: The estimated salary range for this position is $80,000 - $100,000 per year.

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