Clinical Research Associate/CRA - Oncology
- Experience Level
- Experienced (non-manager)
Covance is looking to recruit an experienced UK based monitor (experience in oncology essential) to work in the role of Senior Clinical Research Associate. This role offers excellent exposure to all cancer types.
This Position is: Permanent and Home Based
About the department: The Oncology team has worked on over 500 studies. We are working on several high profile molecular target cancer therapies, traditional chemotherapy as well as those involving targeted therapies with small molecules, immunotherapy and vaccine, virus and gene therapies. The Oncology Clinical Operations team is a smaller business unit so you have genuine opportunities to grow and take on more responsibility whilst knowing you are part of strategically placed Global CRO. Team member expertise is matched to projects where possible and we offer a positive and friendly working environment. Strong team spirit where staff are all pulling together as a cohesive unit with a genuine contribution to global Oncology research.
The successful applicant will be responsible for coordinating Phase I-IV clinical trials in Europe
Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits.
Assist with document submissions to local authorities
To identify potential sites for a proposed study in conjunction with the Project Team, and conduct feasibility assessment of sites as required
Ensure that all study related communication including e-mail is tracked, printed and filed as required
To track patient recruitment by contacting investigators as specified for the study, and discuss potential study risks and opportunities with the Project Manager and liaise with all other appropriate departments within Covance to ensure the smooth running of the study
Full time permanent position in the UK
Applicants must be able to work full time in the UK without restrictions
Please send your CV and cover letter to email@example.com
Please note this is a permanent role and we cannot consider agency submissions or freelancers for these roles
UK accredited Life Sciences degree or nursing qualification is essential
Previous experience of monitoring multiple sites for commercial Oncology studies is a must (Please make your experience clear in your application)
Significant work experience within the CRA job function
Understanding of the principles of ICH GCP and regulatory requirements
Good oral and written communication, organisational skills and personal presentation
The ability to communicate effectively in English
Experience working within a team environment under time and resource pressures
Proven experience in clinical trials with knowledge of SOPs, regulatory reporting requirements and accepted practices
Confident dealing with external and internal clients and providers
It is essential that you have independent monitoring experience in the UK with extensive expertise in the Oncology therapeutic area.
key words oncology, monitoring, clinical research associate
Please contact Marc Joseph on 01753 216664 for further information.
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