Statistics Director job in London

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A global biopharmaceutical company is advertising a vacancy for a Statistics Director position in a home-based capacity. The organisation focuses on developing treatments in the fields of oncology, cardiovascular & metabolic disease (CVMD) and respiratory fields, as well as actively participating in the fields of autoimmunity, neuroscience, and infection. This position offers an exciting opportunity to work with an innovative company whose medicines are used by millions of patients worldwide.

Job Responsibilities:

To lead the strategic, statistical thinking and contributions to the Development Plans, Regulatory Strategy, Health Technology Assessment and Commercial Presentation of company products.
Leadership to statistical staff on the product world-wide so that all work is carried out with regards to company standards and external regulations.
Through partnership with experts, developing design options and providing high quality decision support to enable the business to make informed decisions.
Quantifying the benefit, risk, value and uncertainty of the emerging product profile.
Setting the standards (and enforcing compliance) for statistical work within the product.
Holding CRO/Partners accountable for the high-quality standards of their deliverables.
Represent company and Statistics to Health Authorities and Reimbursement/Payer Organizations for specific projects/indications.
Promote, investigate, develop and implement novel statistical approaches, for relevant statistical issues and/or regulatory guidance and/or value demonstration.
Develop relationships with international opinion leaders, consultants and collaborative groups.
Mentor/coach and support the education and training of Statistics staff in the technical arena.

Skills and Requirements:

MSc/PhD in Statistics or Mathematics (containing a substantial statistical component) with experience in pharma/healthcare or other relevant area.
In depth knowledge of the technical and regulatory requirements related to the role.
Extensive experience of Development, programme design and data analysis and interpretation.
Experience of major regulatory interactions and/or submissions.
Demonstrable multitasking, project management, and execution skills.
Good interpersonal skills, including communication, presentation, persuasion, and influence.
Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
Proficiency with computer skills, such as 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 Emma Adams at +44 203 854 3893 or upload your CV on our website - www.Proclinical.com.

A full job description is available on request.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

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