Senior Statistician

at  Worldwide Clinical Trials

WHO WE ARE

Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers.
Our talented team of 3,500+ professionals spans 60+ countries. We are united in cause with our customers to improve the lives of patients through new and innovative therapies.

YOUR EXPERIENCE

• Experienced professional statistician with a minimum of an MSc in Statistics
• Experienced in guiding/mentoring other statisticians
  To view our other roles, check out our careers page at www.worldwide.com/careers! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

WHAT YOU WILL DO

• Manage the statistics support to one or more projects/sponsor programs of work, ensuring that needs are fully met by expert and timely statistical consultancy and support.
• Provides expert review of study designs, analysis plans and reports.
• Assist sponsors in the design of clinical trials, including statistical sections of the study protocol, randomization methodology and writing statistical analysis plans.
• Liaise with internal departments, sponsors and other third parties regarding statistical issues and reporting requirements.
• Provide project support to the statistics reporting process through the specification/review of tables, figures and listings shells, writing/review of derived dataset specifications and the formatting of report documents and tabulations.
• Lead identifying system and process improvements, and develop and implement solutions to improve the efficiency and quality of clinical study data processing and reporting.

WHAT YOU WILL BRING TO THE ROLE

• Must be computer literate and numerate with a proven ability to adapt to various computer systems
• Hands-on expert level project statistician experienced in providing statistical leadership to projects within clinical research
• Expert in a broad range of statistical applications across all phases (I to IV) of Clinical Research with a thorough knowledge of regulatory standards, SAS and other software applications.
• Well developed consultancy and facilitation skills are required together with key competencies in customer focus, delivering on commitments, building strong relationships, communicating and influencing, embracing innovation and change, building capability and participative leadership