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Lead Statistical Programming Manager

2 months ago

Toronto, Ontario, Canada Everest Clinical Research Services Inc Full time

Company Overview:

Everest Clinical Research Services Inc. is a comprehensive contract research organization (CRO) that offers a wide array of expertise-driven clinical research services to global pharmaceutical, biotechnology, and medical device sectors. We collaborate with renowned companies and engage with some of the most innovative drugs, biologics, and medical devices currently in development.

Established as an independent CRO in 2004, Everest has built a robust foundation as a center of excellence in statistical and data management. Leveraging this foundation, we have successfully evolved into a full-service CRO, with our headquarters situated in the Greater Toronto Area, Ontario, Canada, and additional locations in the Greater New York City Area, New Jersey, USA, Shanghai, China, and Taipei, Taiwan.

Our reputation in the industry is built on delivering high-quality results, exceptional customer service, and the flexibility to meet our clients' diverse needs. As a dynamic organization with entrepreneurial roots, Everest continues to experience remarkable growth and success.

Position Overview:

To sustain our ongoing success in the clinical research arena, we are looking for dedicated, skilled, and client-oriented professionals to fill the role of Senior Manager, Statistical Programming. This position can be performed remotely from anywhere in the USA or at our site in Bridgewater, New Jersey.

Key Responsibilities:

  1. Provide coaching, mentorship, and technical guidance to both direct and indirect subordinate Statistical Programmers and Biostatisticians.
  2. Conduct performance evaluations and create developmental plans for team members.
  3. Contribute to the development and maintenance of standards for database design and SAS datasets related to clinical trial data.
  4. Lead programming efforts for statistical reporting, ensuring adherence to established standards and timelines.
  5. Monitor compliance with programming standards and provide oversight on programming outputs.
  6. Stay updated on industry trends in data standardization and programming best practices.
  7. Assist in the recruitment and training of statistical programming staff.
  8. Participate in the development of statistical programming policies and guidelines.
  9. Engage in project management activities, ensuring timely delivery of programming tasks.
  10. Perform hands-on statistical programming and validation for various clinical trial phases.

Qualifications:

Candidates should possess a Master’s degree or higher in Statistics, Biostatistics, Computer Science, or a related field, along with a minimum of 9 years of experience in clinical trial data processing and statistical programming. A thorough understanding of industry standards and regulatory requirements is essential.

The ideal candidate will demonstrate strong leadership skills, the ability to manage complex programming tasks, and a commitment to maintaining high-quality standards in statistical reporting.