Educational requirements:
- Bachelor’s degree in Life Science, Statistics, Mathematics, or Computer Sciences is required. Master’s degree preferred
Experience and skill requirements:
- Minimum of 5 years of SAS programming experience within a Pharma / Biotech or CRO
- Solid SAS programming skills and experience with CDISC, SDTM, ADaM and Pinnacle 21. Good programming skill in MACRO is needed.
- Experience in the analysis of complex oncology clinical trial data. Knowledge of immuno-oncology is a plus
- Excellent SAS programming skills (including a deep understanding of SAS analytical tools such as SAS/BASE, SAS/STAT and SAS/GRAPH)
- Strong knowledge of relevant internal and external standards and guidance for clinical development (CDISC, EMEA/FDA, ICH- GCP etc.)
- Prior experience filing a BLA or NDA preferred.
- Ability to manage multiple initiatives and shift priorities within a small company environment.
- Excellent interpersonal skills with the ability to work independently and collaboratively in a dynamic team environment.
Location Requirements:
This position can be based either in our Woburn office or be a remote role
- Our Woburn location welcomes hybrid work! Local candidates are expected to be on-site 2 days per week.
- Remote candidates (i.e., living beyond 65 miles of our Woburn HQ) must be open to 10-25% travel to our Woburn HQ, every 6-8 weeks or as business needs require.
Replimune is an equal opportunity employer.
Replimune now requires COVID vaccination disclosure for all US employees.