Associate Director, Clinical Development job in Cambridge, England

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First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

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Phone Number*

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Job type: Permanent

Discipline: VP/Head of Clinical Operations

Location: United Kingdom

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

An opportunity has opened for an Associate Director, Clinical Development to join a global pharmaceutical company based in Cambridge. This role is perfect for a Global Study Leader/Clinical Program manager with an oncology background who is looking for the next step in their career.

Job Responsibilities

Leading cross functional teams of experts in the planning and delivery of a defined clinical program of studies
Work closely with individual study leaders to provide appropriate oversight of a program of studies on behalf of director clinical development (DCD)
Provides clinical operations expertise into the project (e.g. country selection, feasibility, operational input into design, external partner management) to support governance interactions and project start-up.
Support the DCD in providing clinical operations expertise into the development of new business case opportunities for review by governance bodies (cost, timelines, feasibility, risk)
Be early adopters for new ways of working and act as ambassadors for change when leading teams
Identifies and resolves issues within the clinical project ensuring the escalation of the issue to the appropriate individual/functional/governance group for resolution
Lead large or complex deliverables (i.e. indication) and the process to identify and solve operational issues and drive delivery to plan through internal or external partners (Alliance partners, Clinical Research Organizations (CROs), vendors and Academic Research Organizations).

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.
Excellent team building and collaboration skills, for both the Oncology team and the organization.

To Apply

In case you have difficulty in applying or if you have any questions, please contact Jack O'Neill at 0203 846 0646 or upload your CV on our website - www.proclinical.com/send-cv

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