Global Head of Medical Affairs Oncology Diagnostics job in Cambridge, England

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First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

First Name*

Last Name*

Email*

Phone Number*

Country*

Are you an employer or a jobseeker?*

Message

Job type: Permanent

Discipline: Medical Advisor

Location: United Kingdom

This vacancy has now expired. Please see similar roles below...

ProClinical is advertising a vacancy for Global Head of Medical Affairs Oncology Diagnostics position with a global biopharmaceutical company. The organisation focuses on developing treatments in the fields of oncology, cardiovascular and metabolic disease (CVMD). This position offers an exciting opportunity to work with an innovative company whose medicines are used by millions of patients worldwide.

Job Responsibilities

Develop the global scientific and regulatory plan for patient identification solutions for Oncology products and partner with all relevant cross-functional stakeholders to execute the Oncology Diagnostics medical strategy
Develop KEE advocacy and KEE engagement plans in laboratory segments. Lead Scientific Advisory boards and other diagnostics activities at scientific events including major Congresses and Forums.
Interact with professional laboratory societies and advocacy groups for coordination of activities around biomarker education and awareness.
Design and lead medical educational programs with the objective to establish biomarker clinical utility in various HCP segments: oncologists, pathologies, geneticists.
Collaborate with Oncology Medical Affairs to develop and implement plans for RWE generation (ESR, epidemiology studies) in laboratory segments and facilitate their implementation worldwide.
Develop Scientific and Regulatory strategies for biomarker Lifecyle management and biomarker adoption on various testing platforms worldwide.
Support countries with development of local market specific solutions. Lead implementation of local bridging and quality assurance and accreditations studies required by local regulations.
Track guidelines and regulatory landscape for present and future Diagnostic testing in key markets.
Partner with external stakeholders in order to ensure diagnostics solutions are established in laboratories in time for launch

Skills and Requirements

Advanced degree preferred, with at least a Bachelor's in a science-based subject.
6+ years' global trial management experience in a clinical research environment, most of which should be in industry and in Oncology
Substantial experience in early phase therapeutic drug development and proven track record of success.
Multi-dimensional Clinical operations background with capability of devising plans for operational challenges such as site activation, patient enrolment, monitoring oversight, protocol deviation management, data cleaning, site/program budget negotiations, etc.
MS Office

To Apply

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.

In case you have difficulty in applying or if you have any questions, please contact Terence Au at 02038618605 or upload your CV on our website - www.proclinical.com/send-cv

A full job description is available on request.

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