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Clinical Research Associate I

PharmiWeb.jobs: Global Life Science Jobs

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 across various sites. This role presents an exciting opportunity to engage with diverse projects while ensuring adherence to regulatory guidelines and company standards. As a key player in the clinical research team, you will manage site activities, protect patient rights, and maintain data integrity. Join a forward-thinking organization dedicated to transforming drug and device development, where your contributions will make a significant impact on patient care and clinical research. If you are passionate about making a difference in the healthcare landscape, this opportunity is perfect for you.

Qualifications

  • 6 months 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 visits, and closeouts.

Skills

Communication Skills

Organizational Skills

Problem-Solving

Education

University/College Degree in Allied Health Fields

Relevant Experience

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. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. 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 make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. 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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