Dear Allstat,
Key People are currently recruiting for statisticians of all levels, but have the following two new vacancies:
1) Project Statistician paying up to £70k/year + benefits
South East England
PURPOSE OF THE JOB
Develops or assist in the development of protocol designs, clinical plans and data analysis plans in collaboration with physicians, veterinarians, and/or
medical colleagues. Responsible for working with research associates and scientists to establish a reporting database and for analyzing data for these types of studies.
RESPONSIBILITIES
• Operate in collaboration with study personnel to provide input on study protocol, design studies and write protocols for the conduct of each study.
• Assist in or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol, and
conducting the actual analysis once a reporting database is created.
• Collaborate with data management in the planning and implementation of data quality assurance plans.
• Maintain currency with respect to statistical methodology, to maintain proficiency in applying new and varied methods, and to be competent in
justifying methods selected.
• Participate in peer-review work products from other statistical colleagues.
• Collaborate with team members to write reports and communicate results.
• Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, or oral presentations in group
settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings.
• Respond to regulatory queries and to interact with regulators.
REQUIREMENTS
• Qualified to MSc level in a maths or statistics related discipline and proficient in SAS
• Interpersonal communication skills for effective customer consultation
• Teamwork and leadership skills
• Technical growth and application with working knowledge of experimental design and statistics
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables
• Resource management skills
• Business process expertise associated with critical activities (e.g. regulatory submissions)
2) Biostatistician - 12 months contract at excellent hourly rates
Germany
Working on phase 3 diabetes projects you will work closely with the Project Statistician and be full y responsible for the statistical elements of the protocol document, statistical analysis plan writing, validation of analysis programs and output QC, review of clinical trial documents and outputs. You will collaborate with the Lead Programmer and contribute to the validation of statistical programs for across trial analysis. Lastly, you are responsible for developing plans for across trial analyses and presentation of the EU/US regulatory submission packages (summary of clinical efficacy and safety).
Skills and experience required:
MSc / PhD in Statistics or Maths
At least 4 years experience in international clinical development of phase 2-3b studies
Excellent statistical methodological knowledge and excellent communication skills
MUST HAVE PREVIOUS EXPERIENCE IN DIABETES TRIALS
Fluent in English and knowledge of German would be an advantage, but not required.
If you are interested in either of these vacancies then please email Justin Gimblett at Key People on: [log in to unmask] or by telephone on +44(0)1727 817 617. You can see our other vacancies at www.keypeople.co.uk
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