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Senior Director, Global Biostatistics

DirectorDirectorFull TimeRemoteLeadTeam 501-1,000H1B SponsorCompany SiteLinkedIn

Location

United States

Posted

11 days ago

Salary

$160K - $260K / year

Seniority

Lead

No structured requirement data.

Job Description

Senior Director, Global Biostatistics

Veristat

Role Description Participating as a critical part of the Global Operations leadership team, the Senior Director, Biostatistics provides global leadership and strategic direction for the worldwide Biostatistics organization. They are responsible for the successful operation of the Biostatistics department, overseeing the statistical aspects of projects and project teams through the management of functional managers, internal staff, and interaction with Veristat’s executive leadership. - Oversees the development and optimization of departmental processes. - Implements project-specific strategies. - Develops and implements global functional strategies to increase productivity and quality. - Works closely with the head of Statistical Programming to coordinate all statistical and programming activities of client projects. Qualifications - Ph.D. or Master in Statistics, Biostatistics, math-related discipline, or related field, with applied statistics training relevant to clinical trials or health research. - 10 years of relevant work experience. - Strong global or cross-regional leadership experience, with a minimum of 5 years managerial/supervisory experience, preferably in a CRO environment. - Thorough knowledge of International Conference on Harmonization (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines. - Demonstrated ability to thoughtfully solve problems, exercise sound judgment, lead by example and influence without authority. - Demonstrated ability to think “big picture” and strategically leverage expertise, to serve as a consultant and business partner with internal and external customers. - Excellent written and oral communication skills including grammatical/technical writing skills. - Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials. - Working knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical/biotech companies. - Skilled in the use of computer technology, including SAS and other statistical applications, and ability to learn new applications. - Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a fast-paced, team environment. Requirements - Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process. Benefits - Remote working. - Flexible time off. - Paid holidays. - Medical insurance. - Tuition reimbursement. - Retirement plans.

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