Senior Associate Scientist - Therapeutic Antibodies
Regeneron
18 days ago
On-site
Tarrytown, NY
Clinical Research and Development
Responsibilities (During a Typical Day Might Include):
- Perform potency testing of manufacturing, QC, and stability samples.
- Design, develop, and optimize binding and blocking ELISAs to support potency testing of lead protein therapeutics across research and clinical programs.
- Analyze and interpret data using GraphPad Prism and Excel; clearly summarize results for stakeholders.
- Maintain accurate laboratory documentation and data records, performing internal QC checks for team members.
- Prepare data summaries and presentations for internal reporting.
- Communicate project status and results effectively in written and verbal formats.
- Apply strong attention to detail (assays used for clinical testing and regulatory documentation); prior GLP experience is a plus (role is non‑GLP).
Qualifications:
- Bachelor’s or Master’s degree in a scientific discipline with typically 2+ years of relevant laboratory experience (ELISA-based immunoassay expertise highly preferred).
- Strong understanding of drug–ligand binding principles; ability to apply concepts to assay development and troubleshooting (primarily lab-based).
- Proficient in Excel and PowerPoint for data analysis and presentation; GraphPad Prism experience preferred.
- Proven ability to independently analyze, interpret, and summarize complex data with high accuracy.
- Exceptional attention to detail.
- Strong time-management, organizational, and multitasking skills; manage multiple projects in parallel.
- Ability to work independently with minimal supervision and collaborate in a team environment.
- Strong written and verbal communication skills, including presenting data to cross-functional stakeholders.
- Prior GLP/regulated lab experience is a plus (role is non‑GLP).
Application Instructions:
- Apply now.
- Perform potency testing of manufacturing, QC, and stability samples.
- Design, develop, and optimize binding and blocking ELISAs to support potency testing of lead protein therapeutics across research and clinical programs.
- Analyze and interpret data using GraphPad Prism and Excel; clearly summarize results for stakeholders.
- Maintain accurate laboratory documentation and data records, performing internal QC checks for team members.
- Prepare data summaries and presentations for internal reporting.
- Communicate project status and results effectively in written and verbal formats.
- Apply strong attention to detail (assays used for clinical testing and regulatory documentation); prior GLP experience is a plus (role is non‑GLP).
Qualifications:
- Bachelor’s or Master’s degree in a scientific discipline with typically 2+ years of relevant laboratory experience (ELISA-based immunoassay expertise highly preferred).
- Strong understanding of drug–ligand binding principles; ability to apply concepts to assay development and troubleshooting (primarily lab-based).
- Proficient in Excel and PowerPoint for data analysis and presentation; GraphPad Prism experience preferred.
- Proven ability to independently analyze, interpret, and summarize complex data with high accuracy.
- Exceptional attention to detail.
- Strong time-management, organizational, and multitasking skills; manage multiple projects in parallel.
- Ability to work independently with minimal supervision and collaborate in a team environment.
- Strong written and verbal communication skills, including presenting data to cross-functional stakeholders.
- Prior GLP/regulated lab experience is a plus (role is non‑GLP).
Application Instructions:
- Apply now.