
Lead Consultant, Biostatistician Programmer
Ividata Life Sciences
full-time
Posted on:
Location Type: Hybrid
Location: Paris • France
Visit company websiteExplore more
Job Level
About the role
- Lead statistical support and act as the primary point of contact for all assigned study activities
- Ensure the scientific validity and quality of statistical deliverables
- Write and/or review major technical documents
- Program and/or validate statistical analyses
- Perform advanced analyses
- Contribute to the interpretation of results and the development of key messages
- Ensure regulatory compliance
Requirements
- Strong background in Biostatistics
- Proven expertise in SAS programming
- Master's degree (MSc) or PhD in Statistics
- Minimum 8 years' experience in the pharmaceutical industry or a CRO in a lead role
- Excellent command of SAS software
- Deep knowledge of CDISC standards
- Mastery of advanced statistical concepts
- Strong knowledge of Oncology
- Leadership
- Scientific rigor
- Excellent communication skills
- Fluent English (minimum C1 level)
Benefits
- People-focused values
- High-impact assignments
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
BiostatisticsSAS programmingadvanced statistical analysesstatistical deliverablesregulatory complianceCDISC standardsOncology
Soft Skills
leadershipscientific rigorcommunication skills
Certifications
Master's degree (MSc)PhD in Statistics