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Key Responsibilities:
- Lead and support statistical programming aspects of clinical studies.
- Implement and ensure compliance with CDISC standards and regulatory requirements.
- Collaborate with study team members including statisticians and data managers.
Education and Experience:
- Bachelor's or Master's degree in CS, statistics, or related field with relevant experience.
- Oncology therapeutic area experience required.
- Knowledge of ICH, GCP, and clinical drug development process.
About ClinChoice:
- Global full-service CRO with over 28 years of experience.
- Over 4,000 professionals in more than 20 countries.
- Supportive culture focused on quality and professional development.
ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 28 years of experience and over 4,000 professionals in more than 20 countries, with a culture focused on quality, professional development, and supportive collaboration.