About the role
- Lead statistical analysis for clinical trials in immunology and inflammation
- Prepare and review Statistical Analysis Plans (SAPs) and project deliverables
- Ensure high quality database and data capturing
- Monitor progress against project milestones
- Conduct quality control of project deliverables
- May participate in regulatory discussions
Requirements
- 1-2 protocol leading experience (late phase, phase 2-3)
- SAS or R programming skills
- statistical analysis and reporting expertise
- must collaborate with sponsors when required
- ability to manage multiple projects and teams
- experience with clinical trial deliverables and documentation
- career development and progression
- supportive and engaged line management
- technical and therapeutic area training
- peer recognition
- total rewards program
- Total Self culture
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
SASRstatistical analysisstatistical reportingdata capturingquality controlproject deliverablesStatistical Analysis Plansprotocol leadingclinical trial documentation
Soft skills
collaborationproject managementteam management