Sr. Biostatistician Outcome Software, Inc.
THIS JOB HAS EXPIRED Description
Largest CRO in the world with over 27,000 employees globally.
Ranked 6th in InformationWeek 500 Computerworld Magazine?s ?100 Best Places to Work in IT"
Ranked 25th in the inaugural World?s Best Multinational Workplaces list from the Great Place to Work Institute.
Outcome is the late phase and observational study division of Quintiles. We doubled in size last year
Recently went public with one of the most successful IPO?s in the past few years
Seasoned group of 10 who need a leader to drive the group forward and be the technical liaison to leadership.
Experience with process and quality improvement initiatives highly desired
Excellent benefits program including everything from discounts on health club memberships to up to $800 off computer, hardware/software for their home(after 2yrs of service).
Position can be based in either Cambridge, MA or Rockville, MD
Develop protocols, review case report forms (CRFs), and develop analysis plans. Write specifications for tables and analysis files. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Interpret analyses and write statistical sections of study reports.
Perform, advise, and review protocol development, sample size calculation, protocol and 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).
Fulfill 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 RFPs and QIPs; prepare proposal text and attend bid defense meetings for single studies.
Manage customer relationships.
Provide training and guidance to lower level and new staff.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Excellent written and oral communication skills including grammatical/technical writing skills
Excellent attention and accuracy with details
Familiarity with moderately complex and some complex statistical methods that apply to Phase I-IV clinical trials
Strong individual initiative
Strong working knowledge of SAS computing package
Familiarity with other statistical computing packages such as S+, SUDAAN, StatXact
Strong commitment to quality
Ability to effectively manage multiple tasks and projects
Ability to lead and co-ordinate small teams
Proficient at solving complex scientific problems
Ability to establish and maintain effective working relationships with coworkers, managers and clients
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
PhD or educational equivalent in biostatistics or related field and 3 years relevant experience; Master's degree or educational equivalent in biostatistics or related field and 5 years relevant experience; or equivalent combination of education, training and experience
Extensive use of telephone and face-to-face communication requiring accurate perception of speech
Extensive use of keyboard requiring repetitive motion of fingers
Regular sitting for extended periods of time
Primary Location: USA-Massachusetts-Cambridge
Other Locations: USA-Maryland-Rockville
Organization: USA02 - US Clinical Development Svcs
||Cambridge, MA |
THIS JOB HAS EXPIRED