Clinical Research Medical Oncologist

4 days ago


London, Greater London, United Kingdom Real Full time

**About Our Company**

At Real, we are a fast-growing research and consulting company dedicated to assisting with new discoveries in cancer drug development.

The Oncology Medical Monitor will join a team of experienced oncologists, each independently overseeing assigned studies from various locations, including the UK or selected European locations.

This role can be based remotely and requires collaboration with cross-departmental medical monitoring activities to drive best practices across the organization.

Job Summary

We are seeking a highly skilled Clinical Research Medical Oncologist to provide scientific and medical guidance to Oncology project teams, ensuring scientific and client/project goals are met.

The successful candidate will assume Medical and Safety oversight for clinical trials conducted, providing medical input when needed and working collaboratively with other professionals.

  • Provide scientific and medical guidance to Oncology project teams to ensure scientific and client/project goals are met.
  • Act as Medical Monitor for multiple clinical studies, responsible for all clinically related protocol questions, eligibility questions, adverse event evaluation and safety concerns, dosing modification, patient study decisions, medical review of study data, leading data and/or safety monitoring committee teleconferences when applicable.
  • Interact with biostatistics, pharmacokinetics, pharmacovigilance, and regulatory affairs professionals.
  • Contribute to the development and oversight of key internal and external documents related to clinical trial conduct, including clinical trial protocols, informed consents, case report forms, project plans, clinical study reports, and meeting abstracts or publications.
  • Train Oncology staff regarding clinical aspects of drug development, general medical knowledge relevant to the conduct and monitoring of oncology trials, and the mechanism of action and known risks of drugs under study.
  • Provide scientific, clinical, and oncology expertise during new project bid proposal development and defense presentations.
Qualifications
  • Board Certified MD in Oncology/Haematology.
  • Ideally PhD in a relevant research field.
  • Clinical experience in Oncology & active participation in clinical trials.
  • Post-graduate Qualification in Clinical Pharmacology / Pharmaceutical Medicine.
  • Good Clinical Practice (GCP) and familiarity with regulatory requirements.
  • Experience working in either a CRO, biotech, or pharmaceutical company.

Estimated Salary: £80,000 - £120,000 per annum, depending on experience and location. This salary range reflects the industry standard for this position in the UK and European locations.



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