Covance CRA II – ONCOLOGY in Leeds United, United Kingdom

Job Description:

Company: Covance

Location: Home based CRA (Nationwide monitoring)

Closing Date: October 17

Type: Permanent

Salary (£): Competitive

Benefits Full CRA benefits including Car, Private Healthcare & Pension

CRA II – ONCOLOGY

Summary:

CRA II position available to work directly through our CoSource division with a large Pharmaceutical company in the cutting edge area of Oncology, specifically immunotherapy. As an experienced CRA you’ll be involved in initiation, routine & close out visits. Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE!

Requirements

CRA II:

  • Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines

  • Excellent understanding of Serious Adverse Event reporting

  • Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in the UK.

USPs of CRA II role:

  • Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit’ targets

  • You will be invited to attend monthly Oncology meetings at the UK HQ

  • Join a stable team of 30 CRAs across the UK and benefit from outstanding training and development, both initially and throughout your career

  • Join a company where people tend to stay for 6-10 years rather than 1-3!

  • Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance.

  • ONCOLOGY Focussed

Duty Highlights:

As a CRA II you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files. Responsibilities include:

  • All aspects of site management as prescribed in the project plans

  • Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks

  • Negotiation of study budgets with potential investigators and collaboration with Covance legal department with statements of agreements

  • Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.

  • Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems

Other Information:

This CRA II role is a full time & permanent position employed through Covance.

Key words:

CRA II, GCP, Clinical Research Associate, Oncology, Northwest, Birmingham, London, Manchester, Liverpool, Clinical Monitor, Immunotherapy, Cheshire, Cancer Clinical trials

Requisition ID: 70371BR

Job Category: Clinical Research Associate

Locations: United Kingdom - Harrogate, United Kingdom - Leeds, United Kingdom - London, United Kingdom - Maidenhead

Shift: 1

Job Postings: Company: Covance

Location: Home based CRA (Nationwide monitoring)

Closing Date: October 17

Type: Permanent

Salary (£): Competitive

Benefits Full CRA benefits including Car, Private Healthcare & Pension

CRA II – ONCOLOGY

Summary:

CRA II position available to work directly through our CoSource division with a large Pharmaceutical company in the cutting edge area of Oncology, specifically immunotherapy. As an experienced CRA you’ll be involved in initiation, routine & close out visits. Successful candidates will enjoy the benefits of working for a company that values a WORK / LIFE BALANCE!

Requirements

CRA II:

  • Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines

  • Excellent understanding of Serious Adverse Event reporting

  • Previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits) in the UK.

USPs of CRA II role:

  • Unlike some CRA roles you will not be pushed to satisfy unrealistic ‘monthly visit’ targets

  • You will be invited to attend monthly Oncology meetings at the UK HQ

  • Join a stable team of 30 CRAs across the UK and benefit from outstanding training and development, both initially and throughout your career

  • Join a company where people tend to stay for 6-10 years rather than 1-3!

  • Join a genuinely friendly and supportive company where they allow individuals to take ownership of their own performance.

  • ONCOLOGY Focussed

Duty Highlights:

As a CRA II you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files. Responsibilities include:

  • All aspects of site management as prescribed in the project plans

  • Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks

  • Negotiation of study budgets with potential investigators and collaboration with Covance legal department with statements of agreements

  • Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.

  • Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems

Other Information:

This CRA II role is a full time & permanent position employed through Covance.

Key words:

CRA II, GCP, Clinical Research Associate, Oncology, Northwest, Birmingham, London, Manchester, Liverpool, Clinical Monitor, Immunotherapy, Cheshire, Cancer Clinical trials

Education/Qualifications: .

Experience: .

EEO Statement:

EEO Employer Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.