Biostatistics Manager (London, UK)
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: alan.brophy [at] secpharma.com, with a short cover note.
URL: www.datashaping.com/jobs16818e.shtml
Please mention datashaping.com when applying. Thank you.
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