Manage regulatory clinical trial applications and compliance efforts, ensuring biotechnological innovations adhere to regulations while collaborating with cross-functional teams for submissions and strategic planning.

The Director, Contracts Counsel at Eikon Therapeutics oversees contract workflow, drafts and negotiates various agreements, and leads a contracts team. The role emphasizes collaboration across all functions to streamline legal processes and drive operational efficiency.

The Associate Director, Study Start Up will manage clinical trial start-up activities, optimizing timelines, engaging cross-functional teams, and ensuring compliance with industry standards.

The Senior Director, Contracts Counsel will oversee contracting for Eikon, manage a contracting team, enhance workflows, and ensure legal compliance within a biopharmaceutical setting.

Oversee regulatory strategies for CMC aspects in pharmaceutical products, manage a team, and ensure compliance with regulatory agencies.

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

The Associate Director of Pharmacovigilance will lead pharmacovigilance activities, ensuring safety and efficacy of pharmaceutical products, managing vendor relationships, and promoting a culture of safety within the organization.

The Associate Director, Global Safety leads pharmacovigilance activities, ensuring safety and regulatory compliance, and collaborates with cross-functional teams to achieve project goals.

Lead strategy and implementation of enterprise systems for Finance, HR, Legal and Corporate Ops, aligning technology with business goals.