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
Statistical Scientist – Late Phase
Reference Number: 50-830-SS-W
Type of placement: Permanent
Location: Home based or Thames Valley, UK
Our client is the world’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.
As the market leader in leader in interventional IIIb/IV studies, the company offers the expertise and
experience in real-world and late phase research clients require in order to achieve their research
objectives. This includes but is not limited to the design and execution of the following studies:
• Registries: Patient, Disease, Product, Pregnancy
• Post-Approval and Phase IV Studies
• Observational Studies
• Phase IIIb/Expanded Access
• Market Access
• Quality Measurement and Improvement Initiatives
• Benefit Risk Management/RiskMAPS/REMS
• Safety & Surveillance
• Health Outcomes/Health Economics
• Quality of Life
• Patient Reported Outcomes (PRO)
Main Responsibilities:
Perform, advise, and review protocol development, sample size calculation, protocol and Case
Report Form (CRF) review.
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).
Fulfil the Lead role for a group of studies or integrated summaries.
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 groups of studies.
Lead the review of Requests for Proposals (RFPs) and Quality Improvement Programs (QIPs);
prepare proposal text and attend bid defence meetings for single studies.
Manage customer relationships.
Provide training and guidance to lower level and new staff.
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. Qualifications and Experience:
PhD in biostatistics or related field and 3 years relevant experience; Master's degree in
biostatistics or related field and 5 years relevant experience; or equivalent combination of
education, training and experience
Familiarity with moderately complex and some complex statistical methods that apply to clinical
trials and / or observational studies.
Strong working knowledge of SAS computing package
Familiarity with other statistical computing packages such as S+, SUDAAN, StatXact
Ability to effectively manage multiple tasks and projects
Proficient at solving complex scientific problems
Ability to lead and co-ordinate small teams
Ability to establish and maintain effective working relationships with co-workers, managers and
clients
Excellent written and oral communication skills including grammatical/technical writing skills
Excellent attention and accuracy with details
Strong individual initiative
Strong commitment to quality
Our offer:
Competitive basic salary
Bonus
Flexible benefits package including, but not limited to:
Contributory Pension (SIPP)
Private Health Insurance
Permanent Health Insurance
Life Assurance
Additional benefits based on health and well-being
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