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H

Clinical Research Associate

High5 Manchester (5 km)

Service Care Solutions

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Priority Recruitment Manchester (5 km)
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32 - 40 hour

Time Recruitment Solutions Ltd

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Time Recruitment Solutions Ltd Manchester (5 km)
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39 to 43
32 - 40 hour
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H
Clinical Research Associate
High5 Manchester (5 km)
Status Open
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What we ask

Education

No minimum education required

What we offer

Salary

Job description

Clinical Research Associate

Manchester, England, United Kingdom

Full Time


The Clinical Research Associate will support Oncology studies and cover sites across the UK

Apply today and forge a career with greater purpose, make an impact and never stop learning!

Responsibilities

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
  • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
  • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
  • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
  • Collaborate and liaise with study team members for project execution support as appropriate.

Requirements

  • Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
  • In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Life science degree educated or equivalent industry experience
  • Flexibility to travel to sites as required

About the employer

High5
Apply now

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Apply now

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