Associate Director, Statistical Programming at Alexion PharmaceuticalsInc
Mississauga, ON, Canada -
Full Time


Start Date

Immediate

Expiry Date

21 Feb, 25

Salary

0.0

Posted On

23 Jan, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Location: Mississauga, Canada
Job reference: R-216761
Date posted: 01/09/2025
The Associate Director of Statistical Programming will be primarily responsible for overseeing statistical programming activities for multiple clinical studies, maintaining programming infrastructure and ensuring compliance with SOPs to produce quality and timely deliverables. They must possess extensive experience and proven skills in the use of SAS within a Statistical Programming environment and complete knowledge and understanding of the statistical programming processes, procedures, and roles. They will use knowledge of CDISC SDTM and ADaM standards to support Biostatistics in statistical analysis, including generating analysis data listing, tables, and figures and create all files necessary to support an electronic submission in the eCTD format. Additionally, the successful candidate will use hitheirtrong people management skills and supervisory skills to provide direct line management to the statistical programmers, identify training needs and opportunities for optimizing staff utilization and employing the most efficient practices.

Responsibilities

Serve as the Lead Programmer and Manager of the statistical programming efforts. This may include additional responsibilities including, but not limited to:

  • Develop and validate technical programming specifications for analysis datasets using Alexion or ADaM standards.
  • Independently develop and validate programs that generate analysis datasets based on Alexion or ADaM specifications.
  • Develop and validate technical programming specifications for protocol specific efficacy tables, listings, figures/graphs.
  • Independently develop and validate programs that generate protocol specific efficacy tables, listings, figures/graphs using Alexion specifications.
  • Ensuring that the filing of study documentation is maintained to the standard required according to processes and acceptable for audit.
  • Directly support the Clinical and Statistical Programming Director in all aspects of the management and development of the Statistical Programming team. Responsibilities will include, but are not limited to:
  • Participate in the ongoing review of the processes used by the Statistical Programming group to ensure processes are continually complied with and updated as necessary.
  • Create and/or review programming plans, and ensure appropriate resource allocation and prioritization.
  • Act as the primary department contact, when necessary, to ensure that department standards are implemented in all studies.
  • Manage adherence to all company policies, SOPs, and other controlled documents; and ensure all programming activities adhere to departmental standards

Assume direct line management responsibility of the statistical programmers, conducting performance reviews, setting and regularly reviewing objectives, providing guidance and mentoring, and developing and regularly reviewing training and career development plans as required.
Collaborate closely with Biostatistics, Clinical Data Management, Pharmacovigilance, Clinical Operations, and other functions within Alexion to address their needs for programming support.

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