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Clinical Research Associate

Clinical Research Associate

Reference: BBBH29093
Date posted: 30/04/2026
Job details
Specialism
Clinical Operations
Expertise
Clinical Trial Administrator
Location
California, USA
Job type
Contract
Salary
$75.00 to $85.00
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Description

Are you ready to drive the future of clinical research from behind the scenes? Looking to be in the heart of a company where precision meets purpose?

R&D Partners is seeking a motivated and detail-oriented Clinical Research Associate (CRA) to join our team. In this role, you will oversee and monitor clinical trial sites to ensure compliance with protocols, regulations, and quality standards. You will work closely with cross-functional teams to support study execution, site training, and recruitment efforts while maintaining high ethical and professional standards.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Visit clinical trial sites to assess and monitor their performance, ensuring they follow the study protocol and regulations.
  • Provide training and guidance to site staff on study procedures and expectations.
  • Support patient recruitment efforts and address site-related questions or concerns.
  • Review and verify study data for accuracy and completeness.
  • Ensure proper handling, storage, and documentation of investigational products.
  • Assist with regulatory submissions and maintain essential trial documents.
  • Prepare detailed reports on site visits, including any issues or corrective actions needed.
  • Collaborate with internal teams to ensure smooth project execution.
  • Maintain audit readiness by ensuring all required documents are accurate and up-to-date.
  • Support sites during audits and resolve any discrepancies in study data.

Key Skills and Requirements:

  • Strong attention to detail and commitment to quality.
  • Ability to manage multiple tasks and prioritize effectively in a fast-paced environment.
  • Excellent communication and interpersonal skills to build positive relationships with site staff and team members.
  • Knowledge of clinical trial regulations, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Comfortable using technology and adapting to new software tools.
  • Willingness to travel frequently to support site visits and project needs.
  • Proficiency in English and local language (if applicable).

Compensation:

  • $75 to $85 per hour.

For more information, please contact Elliott Croft.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you’ve read and understood our privacy policy, which informs you how we process and safeguard your data – https://www.r-dpartners.com/privacy-policy/

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Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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