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Site Care Partner (Lead CRA) - UK - FSP

TN United Kingdom

Uxbridge

Remote

GBP 50,000 - 70,000

Full time

Yesterday
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Job summary

A leading company in the UK is seeking a Site Care Partner (Lead CRA) to act as the main client contact for investigative sites. This home-based role requires regular travel across the UK and involves managing site activities, ensuring quality, and building relationships with investigators. The ideal candidate will have a background in a related field and strong communication skills.

Qualifications

  • At least 5 years of experience in a related field.

Responsibilities

  • Coordinate study start-up activities and manage site readiness.
  • Support issue resolution and maintain communication with sites.
  • Build positive investigator relationships and ensure compliance.

Skills

Communication
Problem Solving
Relationship Management

Education

Bachelor’s degree or RN in a related field

Job description

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Site Care Partner (Lead CRA) - UK - FSP, Uxbridge

Client: Parexel

Location: Uxbridge, United Kingdom

Job Category: Other

EU work permit required: Yes

Job Reference: bd22f90c5945
Job Views: 3
Posted: 15.05.2025
Expiry Date: 29.06.2025
Job Description:

When our values align, there's no limit to what we can achieve.

Parexel FSP has an exciting opportunity for a Site Care Partner (Lead CRA) in the UK. This is a home-based position with regular travel across the UK.

Job Summary:

The Site Care Partner (SCP) is the main client contact for investigative sites throughout a study's lifecycle. They are responsible for site start-up activities, building and maintaining investigator relationships, supporting site recruitment and operational success, and safeguarding quality and patient safety.

The SCP collaborates with stakeholders for site and country selection, provides local insights, and acts as the "face of the client" to ensure site support, issue resolution, and uphold the client's reputation.

Job Responsibilities:
  • Implement global site and study strategies by qualifying and activating sites.
  • Support country and site selection processes.
  • Coordinate study start-up activities, including site activation and training.
  • Manage site readiness for study initiation and monitor progress.
  • Support issue resolution and communication with sites and internal teams.
  • Oversee site recruitment and ensure enrollment targets are met.
  • Maintain communication with sites for updates and feedback.
  • Review monitoring reports and support documentation submissions.
  • Manage systems related to site activities.
  • Review and update site practices and performance metrics.
  • Ensure quality, compliance, and efficiency in site management.
  • Build positive investigator relationships and develop best practices.
  • Support study closeout activities and site performance evaluations.
  • Travel up to 50% regularly; proficiency in local language and English required.
Education:

Bachelor’s degree or RN in a related field, or equivalent experience (at least 5 years).

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