Lead Statistical Programming Expert

2 weeks ago

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

Everest Clinical Research Services Inc. is a leading contract research organization (CRO) providing comprehensive clinical research services to pharmaceutical, biotechnology, and medical device companies worldwide.

We are renowned for our high-quality deliverables, exceptional customer service, and flexibility in meeting client needs. Our dynamic and entrepreneurial organization continues to experience significant growth and success.

About the Role: Associate Director, Statistical Programming

As an Associate Director, Statistical Programming, you will play a pivotal role in managing clinical trial programs for our esteemed clients. You will provide technical and operational leadership to project teams, ensuring the delivery of high-quality, timely, and budget-compliant results.

Key Responsibilities:
  • Collaborate with senior management to oversee the execution of clinical trial programs, providing strategic direction and guidance to project teams.
  • Represent Everest in business development initiatives and client relationship management activities, fostering strong partnerships.
  • Develop and maintain robust statistical programming standards aligned with industry best practices and regulatory guidelines.
  • Mentor and coach a team of Statistical Programmers, providing technical expertise and guidance to ensure their professional growth.
  • Conduct quality control reviews of statistical programming deliverables, ensuring accuracy and adherence to established standards.
  • Stay abreast of emerging trends in data management and programming practices, recommending and implementing improvements to enhance efficiency and effectiveness.
Qualifications:

We seek a highly experienced and motivated individual with a proven track record in clinical trial data management and statistical programming.

  • Extensive experience implementing CDISC standards for SDTM and ADaM database development.
  • Strong understanding of regulatory requirements for electronic submissions of clinical trial data.
  • Exceptional communication, interpersonal, and leadership skills.
  • Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, or a related field.

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