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H

Clinical Research Associate

High5 Brighton (10 km)

J

Site Manager

JAVA Recruitment Ltd Brighton (10 km)
300
32 - 40 hour

TPF Recruitment

Senior Payroll Administrator

TPF Recruitment Brighton (10 km)
28,000 to 35,000
32 - 40 hour


Solution Search Limited - Construction

Site Manager

Solution Search Limited - Construction Brighton (10 km)
300 to 320
32 - 40 hour

Brakes

Trainee HGV Driver

Brakes Brighton (10 km)
32 - 40 hour

Southdown

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Southdown Brighton (10 km)
13.82
32 - 40 hour

B&B Construction Recruitment Ltd

Facade Site Manager

B&B Construction Recruitment Ltd Brighton (10 km)
65,000 to 68,000
32 - 40 hour

First Recruitment Services

Technical Support Associate

First Recruitment Services Brighton (10 km)
25,000
32 - 40 hour

Swift Recruit

Class 2 HIAB

Swift Recruit Brighton (10 km)
20.52 to 28.72
32 - 40 hour

CPR Recruitment

Site Manager

CPR Recruitment Brighton (10 km)
250
32 - 40 hour

Connect GRP UK

Loft Installer / insulation / Handyman

Connect GRP UK Brighton (10 km)
240
32 - 40 hour

G

Fabric Operative

Gold Group Brighton (10 km)
30,450
32 - 40 hour

Brandon James

CDM Principal Designer

Brandon James Brighton (10 km)
45,000 to 55,000
32 - 40 hour

U

Registered Manager - Sussex

Unicare Complex Care Brighton (10 km)
38,000 to 40,000
32 - 40 hour

K

Traffic Marshall

KDK Recruitment Limited Brighton (10 km)
15 to 15.01
32 - 40 hour
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H
Clinical Research Associate
High5 Brighton (10 km)
Status Open
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What we ask

Education

No minimum education required

What we offer

Salary

Job description

Clinical Research Associate

Brighton, 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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