Senior Clinical Trials Specialist

Adaptive Biotechnologies seeks a Senior Clinical Trials Specialist to support diagnostic clinical trials for clonoSEQ, a minimal residual disease detection assay. The role involves managing trial protocols, coordinating with stakeholders, ensuring regulatory compliance, and serving as the primary contact for trial investigators and participating sites.

Responsibilities

• Maintain and support trial protocol requirements for MRD-related studies with Clinical Trial Managers
• Support MSL team in design and management of clinical trial collaborations
• Coordinate with internal and external stakeholders on specimen processing and data workflows
• Serve as primary contact for trial investigators regarding ordering, specimen handling, and reporting timelines
• Lead customer onboarding and create trial-specific collateral materials

Requirements

• Bachelor's degree or equivalent education and experience combination
• 2–4 years clinical trials, clinical services, or client services experience preferred
• Experience with GCLP trials or FDA-regulated environments preferred
• Strong customer and patient focus with demonstrated HIPAA knowledge
• Familiarity with laboratory and customer service systems such as LIMS and SFDC
• Meticulous attention to detail and data entry skills
• Ability to manage multiple concurrent tasks in a dynamic setting