Freelance CRA - Home Based UK - Oncology

This role will see you monitoring activities at clinical study sites to assure adherence to Good Clinical Practices (GCPs), SOPs, and study protocols across a range of therapy areas.



  • Review regulatory documents as required and prepare site visit reports. 
  • Responsible for multiple projects and must work both independently and in a team environment. 
  • May participate in the study development and start-up process including reviewing protocols, designing and/or reviewing CRFs, preparing Informed Consent forms, developing study documents, organizing and presenting at investigator meetings, working with management on monitoring strategy, and/or developing project-specific CRA training. 
  • May participate in clinical training programs and maintain awareness of developments in the field of clinical research as needed. 



  • BSc in a Life Sciences subject 
  • At least 2 years monitoring experience or combination of on-site monitoring and clinical research coordinator experience. 
  • Customer service orientation. 
  • Sound knowledge of medical terminology and clinical monitoring process. 
  • In depth therapeutic and protocol knowledge as provided in company training. 
  • Ability to perform regionalized travel an average of 65%, depending on project needs. 
  • Excellent verbal and written communications skills. 
  • In depth therapeutic and protocol knowledge as provided in company training. 
  • Excellent interpersonal and organizational skills and attention to detail. 
  • Computer literacy, proficiency in MS Office.


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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