Dear Allstat,
Please find below two newly released jobs based in the South East for the
roles of Associate Director for a large pharma.
If you are interested in these positions and would like more information
please send an updated CV to [log in to unmask]
Associate Director, Statistical Programming
Created due to growth the Associate Director will provide statistical
programming leadership for multiple clinical research and development
projects across the Speciality Pharma portfolio of products at a global
level. They will collaborate with biostatistics in the implementation and
development of project plans ensuring timelines are met and quality is high.
This role is open to a highly technical and strong communicator who is
creative and delivery focused and able to work as part of a cross functional
team.
Key requirements:
Creation of analysis datasets
SAS expert
Phase I- IV experience
Vendor management experience would be an advantage
Previous experience mentoring or supervising a team
Creative and challenging
Associate Director, Biostatistics
The Associate Director, Biostatistics will contribute to product development
strategy and serve as a project representative in the registration and
communication activities. They will manage statistical issues in
communications with regulatory authorities and author statistical sections
of Protocol and Statistical Analysis Plan text. As an experienced
Biostatistician they will review regulatory documents such as CSR’s, as well
as summary documents and provide expert statistical consulting to
development teams.
Key Requirements:
Must have had experience as a statistical lead for a programme of studies
and devised clinical development plans
Academically qualified in Biostatistics or closely related field
Phase II- III experience, IV would be an advantage
Protocol development
Relationship builder, clear communicator and a diplomatic conflict manager
as they will work closely with Medical and Clinical.
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