Part-time Contract - Oncology Monitoring

Responsibilities:

  • Conducting site visits, including pre-study, initiation, monitoring and termination;
  • Ensuring adherence to ICH-GCP and local regulations;
  • Ensuring the completion and collection of regulatory documents;
  • Performing source document verification and query resolution;
  • Oversee study drug management at clinical study sites;
  • Ensure Serious Adverse Event (SAE) reporting according to project specifications;
  • Mentoring junior team members as required.

 

Requirements:

  • A minimum of 2 years of monitoring experience in oncology
  • An advanced level of oncology knowledge
  • Completion of a science-related Bachelor’s degree
  • Excellent knowledge of medical terminology and clinical monitoring process
  • Strong ICH-GCPs knowledge

 

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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