Dear Allstat,
Biostatistics Manager - London
Highly competitive starting salary + Car allowance + Bonus +
Comprehensive benefits
My client is a leading pharmaceutical organisation currently expanding
their UK operations. We seek a skilled Biostatistician professional to
take responsibility for Biostatistics study design/analysis support for
a key compounds and therapeutic areas, operating independently and
handling technically demanding projects as a senior member of the
Biostatistics team. This role also offers the opportunity to lead and
manage a small team.
Role Responsibilities Include:
* Project work including participating in the development of
Clinical Development Plans (CDPs) and the protocol development
process, developing and implementing Statistical Analysis Plans (SAPs),
supervising CROs and interfacing with co-promoters, consulting
with clinical or regulatory affairs groups on strategic issues related
to compound development, study designs, analysis, resource needs and
future plans.
* Managing non-project work including infrastructure development
initiatives and involvement in committees working to develop SOPs and
SWPs to improve quality, efficiency and timeliness of work processes.
* Managing and developing team of direct reports using appropriate
formal and informal processes. Responsible for mentoring individuals
and ensuring efficient allocation of resources within own team.
* Pursuing individual professional development and continuing
education opportunities: reading statistical journals to stay
up-to-date on study design and analysis strategies, undertaking personal
research, attending meetings outside area of direct responsibility to
broaden knowledge base, and proactive involvement in professional
statistical or scientific societies.
Experience required:
* Masters degree in Biostatistics or related discipline required,
PhD preferred.
* Relevant experience in the pharmaceutical industry/CRO
environment.
* Demonstrated excellence in statistical skills across multiple
areas of pharmaceutical biostatistics, with specialised expertise in
some areas.
* Sound understanding of the clinical development process and the
inter-relationships between functional groups.
* History of working in complex team environments with
numerous/diverse stakeholders.
Skills required:
* Good organisation, time management and attention to detail
skills needed to work in a stressful environment under tight deadlines
while maintaining focus on details and quality.
* History of working in complex team environments with
numerous/diverse stakeholders.
* Ability to apply sound judgment and lead problem solving within
a team
* Strong verbal, written and interpersonal communication skills
needed to effectively lead a team toward a common goal
* Statistical programming skills
Non EU candidates requiring UK Visa sponsorship who meet the above
criteria are encouraged to apply.
To apply please forward your CV to [log in to unmask] with a
short cover note. Alternatively call Alan Brophy on 0207 255 66 00 for
further information and a confidential discussion of this opportunity.
Best Regards,
Alan Brophy
SEC Pharma, London
Tel: 0207 255 66 00
Fax: 0207 255 66 01
[log in to unmask]
SEC are an ISO9001:2000 accredited specialist recruitment company
working within the Pharmaceutical, Biotech and CRO industries. If you
are interested to learn more about further appointments within
Biostatistics or Statistical Programming across the UK and Mainland
Europe contact Alan Brophy on 020 7 255 6600 for a confidential
discussion.
SEC Recruitment Limited is acting as an Employment Agency and/or
Employment Business
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