Pharma Senior CRA - Midlands

As an organisation, they are currently running 760 trials through phases I - IV and throughout all of these trials, they are working towards increased Patient Centricity and are committed to providing a best-in-class Patient Experience.

 

Responsibilities:

  • To assist with feasibility studies.
  • Co-ordinate the collection of essential documentation in accordance with ICH/GCP.
  • Assist Project Manager/CRA Manager with establishing and implementing the query resolution process.
  • To ensure that the Investigator maintains all essential documents and that study related documents.
  • TMF filing and review.
  • Manage timely compilation and submission of Ethics Applications and assist in Regulatory applications where required.

 

Requirements:

  • A strong understanding of the clinical process.
  • Previous experience as CRA
  • Early phases experience.
  • Ideally CRO / Pharma experience.

 

This is one of several positions I am currently recruiting for so do please get in touch for a confidential discussion around your current situation and what your ideal next move would be.

 

To make an application please feel free to apply via this website, I am also available on LinkedIn to message regarding the role and will accept all invitations that refer to this advert - look for Dominic Mitchell at RBW Consulting.

 

Please note that owing to the high volume of applications we receive for our roles, if you have not received a response within 48 working hours, do please consider your application unsuccessful.

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