1. 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 Resourcing Solutions, 117 Waterloo Road, SE1 8UL, London, UK
Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch
Providing Flexible Resourcing Solutions
CTC Resourcing Solutions, founded 1997, is a pan-European specialist staffing organisation with
offices in London, Basel 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
Associate Director, Biostatistics – Late Phase
Reference Number: 50-938-ADB-W
Type of placement: Permanent
Location: Thames Valley, UK
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.
Purpose:
Provide direction and guidance in carrying out project assignments, interfacing with clients and
applying advanced statistical methods to project work. Serve as a resource for the department,
ensuring scientific integrity in the application of statistical methodology to clinical trials. Assist the
Director in strategic planning and resource allocation for the department. Act as lead statistician on
major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the
conduct of analyses and preparing integrated clinical and statistical reports. Assist the Director in
proposal development, FTE allocation, budget projections, and client presentation, as needed.
Conduct independent research and teach courses in statistical methodology as resources require.
Main Responsibilities:
 Ensure the high quality and timeliness of deliverables for the late phase biostatistics department
in Europe.
 Participate as Lead Biostatistician on major project(s) including developing/reviewing protocols,
preparing analysis plans, and writing sections of joint clinical/statistical reports, ISSs, ISEs
and/or NDA sections, as required
 Assist in the following: sales meetings as required; overseeing proposal preparation; ensuring
that all proposals bid by the department have an adequate budget, and sufficiently detailed set
of budget assumptions.
 Represent clients at meetings with regulatory agencies or other regulatory meetings; may
participate as a member of a Data and Safety Monitoring Committee.
 Serve as a biostatistical consultant for other members of the department and staff members
from other Biostatistics departments within the company.
 Maintain knowledge and awareness of developments in biostatistics and clinical trial
methodology, and regulatory requirements that impact on analyses.

2. 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 Resourcing Solutions, 117 Waterloo Road, SE1 8UL, London, UK
Tel.: +44 207 193 9972 www.ctcon.ch info@ctcon.ch
 As approved, participate in independent research activities, teaching opportunities,
presentations, and preparation of manuscripts for publication.
 Coordinate and participate in process improvements and inter-office/interdepartmental task
forces; oversee collection and reporting of Biostatistics metrics, implementation of revised work
practices, new guidelines, and new software tools as they become available
Qualifications and Experience:
 PhD in biostatistics or related field and 5 years relevant experience; Master's degree in
biostatistics or related field and 7 years relevant experience
 Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials
 Strong working knowledge of SAS
 Excellent written and oral communication skills with good interpersonal skills
 Excellent problem solving skills
 Excellent presentation skills
 Sound judgment/decision making
 Ability to lead and motivate a team
Our offer:
 Competitive basic salary
 Car Allowance
 Bonus
Flexible benefits package including, but not limited to:
 Contributory Pension
 Private Health Insurance
 Permanent Health Insurance
 Life Assurance
 Additional benefits based on health and well-being
 25 days holiday increasing with length of service