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.

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