CTC Resourcing Solutions is seeking a Senior Global Biostatistician to coordinate statistical work for clinical trials at their client, the world's leading provider of biopharmaceutical services. The position is permanent and can be based in Reading, UK, Dublin, Ireland, Strasbourg, France or be home-based within the EU. Responsibilities include developing analysis plans, performing statistical analyses, advising on database design, and managing projects. Qualifications sought include a PhD in biostatistics, strong SAS and statistical computing skills, and the ability to manage teams and projects. The compensation package includes a competitive salary, bonus, and benefits.
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Senior global biostatistician home based (eu)
1. Providing Flexible Resourcing Solutions
CTC Resourcing Solutions, founded in Basel, Switzerland in 1997, is a specialist staffing organisation based in
Basel, London and Munich, providing flexible resourcing solutions to the pharmaceutical industry across Europe,
with contract and permanent placements in clinical development, data management, statistics, regulatory affairs
and medical marketing.
For one of our clients, we are currently looking for a
Senior Global Biostatistician
Reference Number: 50-13-822-SGB-W
Type of placement: Permanent
Location: Reading, Berks
Dublin, Ireland
Strasbourg, France or home based (EU)
Our client is the word’s leading provider of biopharmaceutical services. With a network of > 27,000
professionals working in over 80 countries, it has helped develop or commercialise all of the top 50
best selling drugs on the market. Through its application of extensive therapeutic, scientific and
analytical expertise, our client helps biopharmaceutical and health sciences customers navigate the
increasingly complex landscape with more predictability to enable better outcomes.
Main Responsibilities:
ï‚· Coordinate the development of analysis plans, table shells, programming and table
specifications, the production of tables, listings and figures, data review and statistical analysis.
ï‚· Perform protocol development, sample size calculation, protocol and Case Report Form (CRF)
review.
ï‚· Advise data management staff on database design, validation checks and critical data.
ï‚· Write statistical sections of integrated reports.
ï‚· Provide expert statistical input into and review of statistical deliverables (i.e. analysis plans,
table shells, programming and table specifications, data review, tables, listings, figures and
statistical sections for integrated reports) and data management deliverables (i.e. database
design, validation checks and critical data).
ï‚· Fulfil the Lead role for single complex studies or groups of studies.
ï‚· Manage project budget and resource requirements. Understand the Scope of Work, budget and
quote assumptions, estimate the work completed, manage scope, and provide revenue and
resource forecasts for single studies.
ï‚· Perform the review of Request for Proposals (RFPs) and pricing; prepare proposal text and
attend bid defence meetings.
ï‚· Manage customer relationships.
ï‚· Provide training and guidance to lower level and new staff.
Qualifications and Experience:
ï‚· PhD in biostatistics or related field; Master's degree in biostatistics or related field; Bachelor's
degree in biostatistics or related field and relevant experience; or equivalent combination of
education, training and experience
ï‚· Excellent written and oral communication skills including grammatical/technical writing skills
ï‚· Excellent attention and accuracy with details
ï‚· Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials
ï‚· Strong individual initiative
ï‚· Strong organizing skills
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK
Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch
2. ï‚· Strong working knowledge of SAS computing package
ï‚· Familiarity with other statistical computing packages such as S+, SUDAAN, StatXact
ï‚· Strong commitment to quality
ï‚· Ability to effectively manage multiple tasks and projects
ï‚· Ability to lead and co-ordinate small teams
ï‚· Ability to solve moderately complex problems
ï‚· Ability to establish and maintain effective working relationships with co-workers, managers and
clients
Our offer:
ï‚· Competitive basic salary
ï‚· Bonus
Flexible benefits package including, but not limited to:
ï‚· Contributory Pension
ï‚· Private Health Insurance
ï‚· Permanent Health Insurance
ï‚· Life Assurance
ï‚· Additional benefits based on health and well-being
ï‚· 25 days holiday increasing with length of service
Should you be interested in the above position and wish to apply, please send your application with your CV,
quoting the above reference number, to our recruitment team at recruitment@ctcon.ch
CTC Clinical Trial Consulting, Studio F7, 80 Silverthorne Road, SW8 3HE London, UK
Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch