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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) delivering a wide array of expertise-driven clinical research solutions to global pharmaceutical, biotechnology, and medical device sectors. We collaborate with leading 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. Expanding upon this foundation, we have successfully evolved into a full-service CRO. Our headquarters are situated in the Greater Toronto Area, with additional locations in the Greater New York City Area, China, and Taiwan.

Renowned for our high-quality deliverables, exceptional customer service, and adaptability to client needs, Everest is a dynamic organization with entrepreneurial roots, consistently experiencing remarkable growth and success.

Position Overview:

To sustain our ongoing success in the dynamic field of clinical research, we are seeking dedicated, skilled, and client-oriented professionals to fill the role of Senior Manager, Statistical Programming.

Key Responsibilities:

  1. Provide coaching, mentorship, and technical guidance to both direct and indirect subordinate Statistical Programmers and Biostatisticians.
  2. Conduct performance evaluations and develop growth plans for team members.
  3. Contribute to the development and maintenance of standards for database design and SAS datasets for clinical trial data.
  4. Lead statistical programming and reporting efforts, ensuring quality and adherence to established standards.
  5. Oversee programming tasks and manage project timelines, ensuring effective communication with clients.
  6. Monitor compliance with industry trends and recommend improvements to programming practices.
  7. Participate in the creation of statistical programming SOPs and guidelines.
  8. Assist in the recruitment and training of statistical programming staff.
  9. Ensure proper archiving of statistical programming information upon project completion.
  10. Engage in high-complexity projects, resolving intricate statistical programming challenges.

Qualifications:

Candidates should possess a Master’s degree or higher in Statistics, Biostatistics, Computer Science, or related fields, along with a minimum of 9 years of experience in clinical trial data processing and statistical programming. A deep understanding of regulatory requirements and industry standards is essential, as is the ability to effectively manage and lead programming projects.

Strong leadership skills, technical judgment, and a commitment to achieving excellence are critical for success in this role.