The Associate Scientist II conducts experiments for drug discovery, focusing on early-stage research and NCE identification, and communicates results effectively.

The Manager, IP Trademarks Paralegal supports the IP department with trademarks, managing docket reports, and legal document management to ensure regulatory compliance.

This role involves statistical programming for clinical studies, collaborating with CROs, analyzing clinical data, and developing standards and processes.

The Senior Manager, Statistical Programming leads programming for clinical studies, ensuring timely analyses, overseeing CROs, and developing SOPs. Requires collaboration across teams and adherence to regulations.

The Pharmacovigilance Contractor will manage pharmacovigilance documents, ensure compliance, support inspections, and collaborate with cross-functional teams. The role emphasizes quality improvement and regulatory adherence.