Top Remote Pharmaceutical Jobs in Seattle, WA

The Director is responsible for developing and overseeing global engagement strategies with external stakeholders, ensuring effective communication and governance across functions.

The Manager, Global Product Quality oversees compliance with GMP and DEA regulations for controlled substances, ensuring quality and regulatory oversight throughout the product lifecycle and collaborating with cross-functional teams.

Lead Otsuka's digital content and social strategy, enhancing corporate digital presence through analytics, storytelling, and website governance. Manage social media strategies and executive presence while ensuring compliance and messaging accuracy.

The Senior Clinical Research Associate oversees site management and monitoring for clinical trials, ensuring compliance with GCP, patient safety, and quality execution of studies. Responsibilities include managing operational aspects, training site personnel, addressing protocol issues, and conducting monitoring activities.

The Feasibility Study Manager oversees global feasibility assessments, transforming questionnaires into surveys, verifying investigator readiness, managing survey execution, and ensuring successful project completion.

The Senior Director of PV Client Support manages client services, oversees team operations, sets strategic goals, and ensures compliance while fostering team development.

The GMP Auditor will plan and conduct GMP audits, serve as an SME on FDA regulations, and create documentation for clients.

Lead cross-functional teams to deliver project plans in molecular imaging, optimize processes, and modernize business operations reporting.

The Lead, Clinical Supply Chain Planning role involves planning and scheduling clinical batches, ensuring timely distribution of products, maintaining documentation, and collaborating with various teams to optimize supply chain processes.

This position is for potential future opportunities in the Commercial field at Day One Biopharmaceuticals. Candidates should submit their resumes for consideration as the company grows.

This role encourages interested candidates to submit resumes for future opportunities in various product development areas including clinical operations and regulatory science.

Day One Biopharmaceuticals invites candidates to submit their resumes for future opportunities in various operational roles, emphasizing a commitment to equal employment. No immediate openings are available.

The Senior Director of Marketing will design and implement marketing strategies for rare disease products, lead a team, ensure compliance, and manage budgets.

The Associate Director will manage commercial data assets, ensuring data quality and governance while liaising between stakeholders and data engineering teams.

The Senior Project Manager oversees project execution in drug development, ensuring alignment with company strategies, managing budgets, and facilitating cross-functional collaboration to meet objectives.

The Director of Upstream Product Marketing leads the commercial vision for Telix's late-stage PSMA imaging portfolio, shaping strategies, aligning teams, and driving growth initiatives while effectively communicating with stakeholders.

The Director of Upstream Product Marketing is responsible for driving early-stage commercial strategy for PSMA imaging products, market assessments, business case development, and cross-functional leadership.

The Operations Associate manages project launches, client onboarding, and cross-functional communication to ensure operational excellence and smooth client interactions.

The Sr. Director, Commercial Sales will drive business development, build client relationships, execute strategies, and collaborate with stakeholders to meet revenue targets in the cell and gene therapy sector.