- Provision of scientific and medical guidance to project teams to ensure that scientific / client / project goals are achieved.
- Act as Medical Monitor for multiple clinical studies, advising upon protocol and eligibility questions, adverse event evaluation and safety concerns, dosing modification, medical review of study data and leading data review and / or safety monitoring conferences.
- Contribution to the development of key documents such as study protocols, ICFs, CRFs, project plans etc.
- Training staff on the clinical aspects of drug development, general medical knowledge related to the conduct and monitoring of oncology trials and the mechanism of action and known risks of drugs under study.
- Local medical registration with a license to practice.
- Oncology experienced gained in both a healthcare setting and in industry.
- Board certification in Oncology or Haematology.
- Pharmacovigilance experience.
- Willing to travel internationally for a few days each month.
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Medical Monitor, Oncology
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Float Clinical Team Coordinator
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Clinical Trial Co-ordinator
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Clinical Trial Co-ordinator
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Medical Monitor, Oncology - London, United Kingdom - CK Group
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Description
CK Group are looking for a Medical Manager, Oncology to join a long-established and well recognised Clinical Research Organisation specialising in Oncology. This will be a field based role in the UK, Ireland, Sweden, Italy or Spain.RESPONSIBILITIES:
As Medical Manager, Oncology you will provide medical and safety oversight for assigned studies.
Key duties will include:
As Medical Manager, Oncology you will require:
BENEFITS:
Competitive salary plus excellent benefits.
Apply:
It is essential that applicants hold entitlement to work in the country you will be working in. Please quote job reference in all correspondence.