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Job Details

Clinical Trials Monitor / Compliance Oversight Advisor - London

Company: University College London
Location: London, UK
Reference: 1782278
Closing Date: 31 Jan 19
Type: Full Time
Salary (£): Competitive
Benefits: Excellent

Job Summary:

The Joint Research Office (JRO) was established in August 2006. The Office has a central focus on providing research management and governance support to biomedical research studies across both Institutions and ensures researchers continue to contribute to the high scientific and cutting edge research that currently exists.

Requirements:

The JRO provides research support services to facilitate compliance with regulations for an extensive portfolio of clinical research studies conducted across the organisation(s). A particular focus within the JRO is clinical trials (CTIMPs) and the trials team is involved in a variety of trials functions such as sponsorship authorisation, negotiating sponsorship agreements, supporting regulatory authorisations, implementing a pharmacovigilance system to support the UCL and UCLH clinical trial portfolio, training researchers, project planning and management to ensure successful conduct of research from concept to trial completion and publication.

The Clinical Trials Monitor/Compliance Oversight Advisor will be responsible for ensuring oversight of the clinical trials portfolio sponsored by UCL. This post will also be responsible for ensuring trials are compliant with GCP, UK regulations and research frameworks.

 

Key Requirements

The successful applicant will hold a first degree in biomedical science or significant equivalent experience as well as proven ability to monitor biomedical projects to meet ICH GCP standards. 

Good working knowledge of EU pharmacovigilance requirements and Good Manufacturing Practice (GMP) is also essential for this post.

 

Further Details

A job description and person specification can be accessed at the bottom of this page. To apply for the vacancy please click on the ‘Apply Now’ button below.

If you have any queries regarding the vacancy please contact Helen Cadiou – Head of Quality Assurance on 020 3447 9940.

If you have any queries regarding the application process please contact Curtis Alleyne – Operations Manager (curtis.alleyne1@.nhs.netor 020 3447 2104). 

 

We particularly welcome applications from black and minority ethnic candidates as they are under-represented within UCL at this level.

We will consider applications to work on a part-time, flexible and job share basis wherever possible.

Apply for this job: Clinical Trials Monitor / Compliance Oversight Advisor - London

Contact Information:

Address:  Joint Research Office - Clinical Research Support
London

England

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