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Clinical Research Associate I

Fortrea

Maidenhead

On-site

GBP 80,000 - 100,000

30+ days ago

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Job summary

An established industry player is seeking a motivated Clinical Site Monitor to oversee clinical studies at various sites. This role presents an exciting opportunity to contribute to diverse projects while ensuring adherence to regulatory guidelines and company SOPs. The ideal candidate will possess a university degree or relevant experience in allied health fields, along with strong communication and organizational skills. Join a collaborative workspace where personal growth is nurtured, and make a meaningful impact in the field of clinical research. If you are passionate about overcoming barriers in clinical trials, this position is perfect for you.

Qualifications

  • 6 months of experience in Site Management or CRA roles.
  • Basic knowledge of Regulatory Guidelines and clinical trial processes.

Responsibilities

  • Oversee study site monitoring and ensure compliance with protocols.
  • Manage site activities including initiation, monitoring, and closeouts.

Skills

Communication Skills

Organizational Skills

Problem-Solving

Education

University/College Degree in Allied Health Fields

Tools

Data Integrity Checks

Job description

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. Conducting operations in ~100 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

Fortrea is seeking a motivated and detail-oriented Clinical Site Monitor to manage and oversee clinical studies at various sites. This role offers an exciting opportunity to work on diverse projects while ensuring compliance with regulatory guidelines, project plans and company SOPs.

Key Responsibilities:

  1. Oversee study site monitoring and ensure compliance with protocol requirements.
  2. Manage site activities, including site initiation, monitoring visits and closeouts.
  3. Ensure proper informed consent and patient protection.
  4. Perform data integrity checks and maintain study files.
  5. Assist with feasibility work, investigator recruitment and vendor coordination.
  6. Support senior team members and mentor new employees.
  7. Track and report Serious Adverse Events (SAEs) and support quality control efforts.

Qualifications:
  1. University/college degree or relevant experience in allied health fields.
  2. 6 months of experience in a related role (e.g., Site Management, CRA).
  3. Basic knowledge of Regulatory Guidelines and the clinical trial process.
  4. Strong communication and organizational skills.
  5. Valid driver’s license.

If you're ready to make a real impact in clinical research, apply now!

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com.

Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We encourage all to apply.

For more information about how we collect and store your personal data, please see our Privacy Statement.

If, as a result of a disability, you require a reasonable accommodation to complete your job application, pre-employment testing, job interview or to otherwise participate in the hiring process, please contact: taaccommodationsrequest@fortrea.com. Please note that this e-mail address is only for job seekers requesting an accommodation. Please do not use this e-mail to check the status of your application.
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