Ref #: 26904

Employment type: Permanent - Full-Time

Location: West Midlands in the UK

Posted: 27-Apr-2021

Description

The Senior CRA role
• Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
• Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
• Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
• Managing sponsor generated queries efficiently and responsible for study cost effectiveness
• Dependent on level of experience you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects

What you need
• 3 to 5 years of site monitoring experience in phase I-III trials as a CRA
• UK-based experience and UK working eligibility
• Knowledge of ICH GCP guidelines and expertise to review and evaluate medical data
• Degree (BA/BS/BSc) in life sciences or qualified nurse preferable
• Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
• Ability to produce accurate work to tight deadlines within a pressurized environment

What we offer
• Excellent salary package
• Company benefits to include car allowance, pension, health insurance, pension, etc.
• Scope for career progression
• Great technology to work from home
• Family friendly

For more information, please contact me at Elisabeth.Knighton@DOCSGlobal.com


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