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Please reply to the details below, rather than to me Thanks Chintu -------------------------------------------------------------------------------------------------------------------------------------------------------- In the complex world of drug development, PharmaNet/i3 is exactly where you need to be. With offices in more than 30 countries around the world, PharmaNet/i3 has the resources to conduct any study; from a large multi-country, multi-language clinical trial today, to a smaller regional study tomorrow. PharmaNet/i3 works for you on trials of any size, anywhere around the world. Working in partnership with our client Boehringer Ingelheim, this unique role plays a key part in the continual support of one of our Functional Strategic Partnerships. As such we are able to offer all the advantages of working for a top-five CRO combined with the benefits of operating as an integrated member of a multi-functional client-specific clinical team. You will be responsible for: • As an authority in the field of statistical programming using SAS, providing statistical programming and other expert technical support to the sponsor, programmers, and other department staff as needed. • Supervise staff programmers and contribute to performance reviews. May have line management responsibilities. • Manage or lead assignments and programming personnel on single or multiple projects. • Assume overall responsibility for the successful execution of projects including adherence to timelines and budgets, as well as the quality of deliverables. • Ensures that activities and processes performed are conducted according to company and sponsor requirements. • Review Protocol, Statistical Analysis Plan (SAP), and shells for tables, listings and figures for projects. • Work directly with our client in the definition, execution, and review of statistical programming projects. • Partners with project statistician and programming team on the implementation of the statistical analysis. • Lead program validation for each project and assists with statistical quality assurance review. • Review deliverables before transfer to either internal or external client. • Solicit feedback on project profitability from manager or project manager in order to assess and address productivity issues. • Undertake statistical programming consultancy for sponsor company. • Lead strategic departmental development and mentorship activities, including training for department members. • Interact with other departments, such as Biostatistics and Project Management, to ensure a high level of sponsor satisfaction through successful execution of projects. • Lead department activities associated with internal & external audits. • Provides leadership in the development of efficient programming processes within the department. • Develop software for standard systems. • Lead technical initiatives at a local and global level. • Maintains ongoing awareness of developments in statistical programming techniques and regulatory developments relevant to clinical trials and ensures that colleagues are kept informed. And be able to meet the following requirements: • B.S. degree required, M.S. degree preferred. • Extensive experience in SAS programming for pharmaceutical projects demonstrated by the ability to lead multiple complex projects with large teams located across multiple sites. • Possesses strong project management skills. • Demonstrated working knowledge of clinical drug development and good programming • practices. • Proficient in industry standards, medical terminology, and clinical trial methodologies. In return you can expect: • The flexibility to be home or office based • A competitive remuneration package with excellent benefits. • A commitment to your development and training, with the opportunity to progress your career within a market leading and innovative organisation. • The opportunity to work within a successful and rewarding environment. To apply or find out more please contact Frances Wells at [log in to unmask] or call +44 (0) 1628 408444. Frances Wells Senior Recruiter, EMEA Please note new e-mail address [log in to unmask] Star House, 20 Grenfell Road, Maidenhead, Berkshire, SL6 1EH, UK P: +44(0)1628 408444 M: +44(0)7891 182660 [log in to unmask] | www.pharmanet-i3.com You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.