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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 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 evolved into a full-service CRO, with our headquarters situated in the Greater Toronto Area, Ontario, Canada, and additional offices in key locations.

Known for our commitment to high-quality deliverables, exceptional customer service, and adaptability to client needs, Everest is a dynamic organization with an entrepreneurial spirit, consistently achieving remarkable growth and success.

Position Overview:

To sustain our momentum in the clinical research arena, we are in search of dedicated, skilled, and client-oriented professionals to take on the role of Senior Manager, Statistical Programming. This position can be performed remotely across the USA or at our designated office location.

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 creation and upkeep of standards for database design and SAS datasets related to clinical trial data.
  4. Lead statistical programming and reporting initiatives, ensuring the execution of programming tasks aligns with established standards.
  5. Oversee programming efforts for designated client clusters, ensuring compliance with industry standards.
  6. Stay informed on industry trends and advancements in data and programming practices, recommending improvements to existing standards.
  7. Assist in the recruitment and training of statistical programming staff.
  8. Facilitate the archiving of statistical programming information post-project completion.
  9. Engage in hands-on statistical programming and validation for various clinical trial phases and regulatory submissions.
  10. Provide training and mentorship to junior team members, fostering their professional development.

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 relevant experience. A deep understanding of clinical trial data processing, statistical programming, and regulatory requirements is essential. Strong leadership skills and the ability to manage complex projects are crucial for success in this role.