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The Associate Director of Biostatistics will design and analyze clinical trials, lead statistical efforts, and mentor team members while ensuring regulatory compliance and collaboration with cross-functional teams.

The Senior Medical Writer will lead the development of clinical and regulatory documents, ensuring accuracy and compliance while collaborating with cross-functional teams to manage project timelines and improve writing processes.

The Associate Director, Study Start-Up leads feasibility activities for clinical trials and ensures efficient study start-up, collaborating across teams and optimizing processes.

Lead regulatory strategy and compliance efforts, ensuring biotechnological innovations align with regulations. Collaborate with teams for product development, manage submissions, and oversee quality assurance.

Lead the computer system validation and quality assurance efforts in biotech, ensuring compliance with regulatory standards, and managing the QA team.

The Senior Research Associate II will conduct cell culture experiments, support target validation for Parkinson's disease, and maintain detailed records.

The Senior Director of Drug Safety and Toxicology will lead safety assessments, manage toxicology studies, and author regulatory documents while ensuring compliance with guidelines during project phases.