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Senior Clinical Research Associate

JR United Kingdom

York

Remote

GBP 50,000 - 56,000

Full time

2 days ago
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Job summary

A leading CRO is seeking a Senior Clinical Research Associate to oversee site management across clinical trials. The candidate will be instrumental in ensuring compliance, conducting site visits, and collaborating with investigators to enhance trial success. This remote role is ideal for those with a strong background in clinical research and patient management.

Qualifications

  • Minimum 3 years CRA experience required.
  • Equivalent experience will be considered.
  • Strong understanding of clinical research practices is essential.

Responsibilities

  • Manage investigator sites throughout the study lifecycle.
  • Conduct feasibility and monitoring visits, primarily for phases 1-3.
  • Review regulatory documents and ensure compliance.

Skills

Knowledge of medical terminology
Patient management
Drug therapy understanding
Clinical research methodologies

Education

Bachelor of Science in a health-related field

Job description

Senior Clinical Research Associate, York
Client:

RBW Consulting

Location:

Remote in UK

Job Category:

Other

Work Permit Required:

Yes

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:
  • Job Title: Senior Clinical Research Associate
  • Location: Remote in UK
  • Salary: £50,000 - £56,000 plus car allowance or company car
  • Company: Global CRO

RBW Consulting is seeking a Senior Clinical Research Associate to join a renowned CRO with a European culture, focusing on unmet disease targets and advancing clinical research. The role involves managing investigator sites through the study lifecycle, conducting site visits, preparing for meetings, and ensuring compliance and safety.

Key Responsibilities:

  • Manage investigator sites throughout the study lifecycle (start-up to close-out)
  • Conduct feasibility, initiation, monitoring, and closeout visits (mainly phase 1-3)
  • Attend investigator meetings and coordinate clinical supplies and safety follow-up
  • Perform source data verification and review case report forms
  • Review regulatory documents
  • Report and follow-up on adverse events
  • Assess patient recruitment and retention

Qualifications:

  • Bachelor of Science in a health-related field or equivalent
  • Minimum 3 years CRA experience
  • Knowledge of medical terminology and patient management
  • Basic understanding of drug therapy and clinical research methodologies

Application Process:

Please click ‘Apply’ or contact Joe Pearce for further information.

About RBW Consulting:

RBW Consulting is a life sciences talent and strategic consultancy dedicated to supporting health innovations. We value diversity, support our employees, and are committed to equal opportunity employment. We prioritize talent and potential over resumes and strive to build a diverse workforce.

Note: If you are not a passport holder of the country for the vacancy, you might need a work permit. Check our Blog for more information.

Applications should be submitted via the 'Apply now' button. Do not provide bank or payment details when applying.

Created on 04/06/2025 by JR, United Kingdom

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