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The National Director will develop and execute a US thought-leadership engagement plan for Nephrology, collaborating closely with several teams to drive strategic priorities and manage resources.

Lead PV Scientist for assigned product(s), providing scientific oversight of signal detection/management, RMPs (core and EU), and aggregate safety reports (DSURs, PBRERs). Coordinate cross-functional safety activities, respond to regulatory requests, support filings, manage processes and improvements, and (where applicable) manage and mentor PV team members to ensure global pharmacovigilance compliance.

The Associate Director, PV Scientist will lead safety surveillance, manage risk plans, oversee aggregate safety reporting, and ensure compliance with global regulations while mentoring a team.

The Senior Manager oversees payer communications, develops medical materials for stakeholders, and collaborates across functions to ensure compliance in scientific communications surrounding multiple sclerosis publications.

Leads statistical programming activities and oversees analysis dataset specifications, ensuring adherence to standards and timelines. Collaborates with various teams and manages resources, delivering high-quality outputs for drug development projects.

The role involves leading U.S. Alzheimer's HCP Marketing strategy, developing brand plans, engaging with leadership, and fostering key relationships to improve patient outcomes.

The Study Manager leads biomarker and bioanalytical operations across clinical studies, ensuring high-quality data delivery and compliance during drug development.

The Sr. Associate II oversees quality assurance operations, supports compliance audits, coach teams, and leads investigations to improve processes and ensure product safety.

The Senior Analyst leads statistical programming activities, ensures quality and timely delivery of statistical outputs, authors specifications, manages programming deliverables, and collaborates with teams to implement data strategies.

The Manufacturing Engineer III supports solid dose manufacturing by troubleshooting equipment, improving performance, leading projects, and ensuring CQV activities are executed successfully.