Top Biotech Jobs in Spokane, WA

The Clinical Trials Manager oversees clinical studies, manages protocol compliance, develops study documents, supports site management, and assists in staff training and clinical trial updates.

The Value Stream Quality Manager oversees product lifecycle quality, ensuring compliance with regulations for biotechnology products. They manage quality control and improvement processes while collaborating cross-functionally with various departments to support both internal and external GMP productions.

The Territory Manager will develop and execute sales strategies for GE HealthCare's intra-operative ultrasound products, manage existing accounts, achieve sales targets, and maintain customer relationships.

Designers create equipment room layouts using AutoCAD, collaborating with Project Managers, ensuring compliance with standards, and producing quality documentation.

The Director of Corporate Partnerships will drive relationships with wholesalers and GPOs, maximizing opportunities and ensuring client satisfaction while collaborating with internal teams to align on strategic priorities.

The Business Development Manager will drive prospecting efforts, identify clients in life sciences, manage a sales pipeline, close deals, and interact with key stakeholders to achieve sales targets.

The Associate Genealogist will conduct genealogical research, manage tasks to meet deadlines, and communicate effectively with clients in German and English.

Conduct expert genealogical research, produce research logs and reports, manage client projects, and maintain high standards of quality and communication.

As a Sr. CRA II, you will monitor clinical trial sites, ensuring compliance with protocols, managing data integrity, and reporting adverse events. You'll also assist with training and coordinate local projects as needed, requiring 5+ years of clinical monitoring experience, particularly in oncology.

The Sr. CRA II is responsible for monitoring clinical trials in oncology, ensuring protocol adherence, data integrity, and site management. This role includes coordinating clinical projects, conducting site visits, and training staff.

The Sr. CRA II will oversee study site monitoring, ensure protocol compliance, manage data integrity, and coordinate clinical projects while traveling frequently.

The Senior Director leads portfolio and program management for global execution across clinical development programs, ensuring alignment with corporate objectives and resource optimization. This role requires strategic decision-making, governance oversight, and cross-functional collaboration with various teams to drive successful advancement of gene therapy programs.

Lead and mentor oncology program management teams, develop global product strategies, manage projects, and drive process improvements in drug development.

Collaborate with cross-functional teams to build and maintain Valo Health's large-scale computational platform for drug discovery, focusing on software infrastructure and architecture.

The Manager, Account Development increases market awareness and customer base through direct client contact, strategy implementation, and collaboration with the Business Development Team.

Lead a team of Client Success Managers to manage multiple pharmaceutical accounts, drive retention and expansion, execute growth plans, oversee campaign strategy and MLR approvals, collaborate cross-functionally, run QBRs, and ensure account health and revenue growth.