Clinical Trial Design Methodology Expert - Cambridgeshire

Recruiter
CK Clinical
Location
Cambridgeshire
Posted
10 Feb 2018
Closes
15 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Stephanie Maccioni is working with an innovative global Pharmaceutical company for an experienced Clinical Trial Design Methodology Expert. This role would be on a permanent basis in their HQ in Cambridgeshire, it can also be based in other sites within the EU/US. The position is office based and includes an excellent salary plus benefits.

Main duties and responsibilities:
-As a key clinical trial methods expert you will provide consultancy to, and collaborate with, fellow statisticians as well as medical scientists and other key roles across the business.
-You will also lead and participate in more strategic activities such as capability build projects, which deliver broad improvements to the way clinical trials are designed and analysed.
-You are expected to develop and implement new methodology and interact with external scientists and regulators, through publications, presentations and cross-industry collaborations.
-You will provide 'just in time' consulting and mentoring primarily for clinical trial design questions, proactively identify new areas where Statistical Innovation can add value, develop collaborative relationships with the external scientific/academic community, as well as innovate in collaboration with groups.
-You will thus have the opportunity to use your statistical expertise to influence the design of key clinical trials that are instrumental both to patients and the wider scientific community.
-In addition, you will contribute to or lead capability build in one or more of the following statistical areas: Advanced/adaptive clinical trial design, multiplicity, subgroups and biomarkers, decision analytics.
-You will work regularly in a global, cross-skilled setting, with manager, colleagues and customers spread over 3 research sites.

Key Requirements:
-Strong track record of research and methodological development in Statistics, supported by scientific publications in first class statistical journals
-Documented ability of delivering innovative statistical solutions in an applied environment (preferably related to clinical trial design)
-High level of competence in global and cross-skilled collaborative working
-An urge to apply your scientific competence on practical problems, for the benefit of patients

A full job spec is available upon request

Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.

CK Group is an Equal Opportunities employer and welcomes applications from all who meet our selection criteria.

If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference CL41243 in all correspondence.

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