
Senior Statistical Data Analyst and CDISC Specialist
1 day ago
Job Opportunity:
We are seeking a highly skilled Senior Statistical Data Analyst and CDISC specialist to support our clinical trial programming activities. The ideal candidate will have expertise in statistical programming, data management, and regulatory compliance.
Main Responsibilities:
- Clinical Trial Programming: Develop and maintain high-quality SAS programs for clinical trials, ensuring accuracy and compliance with study specifications.
- CDISC Standards Implementation: Implement and maintain CDISC standards, including SDTM and ADaM, to ensure seamless data exchange and integration.
- Mentorship and Leadership: Provide guidance and support to junior team members on programming best practices, data management, and regulatory compliance.
- Collaboration and Communication: Work closely with cross-functional teams to ensure timely delivery of high-quality deliverables and effective communication of project progress.
Required Skills and Qualifications:
- Strong background in statistical programming, data management, and regulatory compliance.
- Proficiency in SAS programming, including experience with SDTM and ADaM.
- Excellent understanding of CDISC standards and ICH guidelines.
- Strong analytical and problem-solving skills, with ability to work independently and as part of a team.
Preferred Skills:
- Experience with other statistical software, such as R.
- Familiarity with various therapeutic areas and different phases of clinical trials.
- Experience presenting at conferences or publishing in professional journals.
About the Role:
This is an excellent opportunity for a seasoned statistical data analyst to take on a leadership role and contribute to the success of our clinical trial programming activities.
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