Associate Director Statistical Programming Oncology job in City of London, 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?*

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Job type: Permanent

Discipline: Programming

Location: United Kingdom

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

Proclinical is actively seeking an Associate Director of Statistical Programming with a focus on Oncology. This role is integral to putting global statistical programming strategies into action. The successful candidate will work closely with the Clinical Development teams to ensure project deliverables timelines are met.

Responsibilities:

Work alongside the Director of Statistical Programming to put statistical programming strategies into place.
Help with the creation and application of a programming ecosystem.
Work with the Clinical Development teams and the organisation to meet all project deadlines.
Solely execute and oversee the creation and authorisation of programming deliverables.
Anticipate resource needs and work with management to ensure adequate long-term resource allocation.
Ensure quality control on all process and technical activities related to programming.
Participate in the development of a global programming standard library.
Cooperate with Biostatistics to develop, apply and maintain appropriate statistical applications.
Provide programming support to regulatory submissions.

Key Skills and Requirements:

Advanced degree in Mathematics, Computer Science, Biostatistics or other related discipline is preferred.
Proven working history in a pharmaceutical industry or another clinical research setting.
Strong understanding of statistical programming.
History in Oncology or infectious disease therapeutic areas and submission is preferred.
Project management experience.
Understanding of FDA, EMA, ICH, and global regulations and guidelines.
Solid knowledge of industry standards applicable to clinical study data and reporting on clinical trials, including CDISC standards.

If you are having difficulty in applying or if you have any questions, please contact Heidi Hennigan on h.hennigan@proclinical.com.

Apply Now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.