Sr. Project Manager for LDT launch
Confirmed on the employer's own hiring board on Oct 31, 2026. First seen by Alion on Feb 13, 2026. Accuragen scores A on the Alion truth index.
AccuScan Sciences is a biotechnology company developing whole-genome-sequencing-based liquid biopsy tests for minimal residual disease detection and precision oncology applications. Our work sits at the intersection of genomics and precision oncology, with a focus on advancing diagnostic capabilities that can help inform patient care and clinical decision-making.
As Sr. Project Manager, you will help drive cross-functional programs that support the development and operational readiness of complex diagnostic initiatives. This role plays an important part in keeping teams aligned around shared goals, maintaining momentum across interconnected workstreams, and supporting effective coordination among scientific, operational, regulatory, and quality-focused stakeholders.
Responsibilities
- Maintain integrated project plans across cross-functional teams.
- Monitor deliverables and dependencies aligned to product objectives.
- Ensure adherence to development timelines and escalate risks as needed.
- Facilitate cross-functional project meetings and track action items.
- Manage the timeline for CLIA certification and CAP accreditation readiness.
- Coordinate cross-functional activities required for inspection preparedness.
- Align laboratory operational readiness with accreditation and inspection timelines.
- Proactively identify project risks and mitigation strategies.
- Maintain clear communication across stakeholders.
- Serve as central point of coordination for project-level reporting.
Requirements
Qualifications
· Bachelor’s degree required; PMP or equivalent certification is a plus.
· 8+ years of project or program management experience in biotech, diagnostics, or life sciences
· Experience with cross-functional milestone tracking and coordinating cross-functional teams required.
· Experience working with laboratory operations, regulatory, and quality teams required.
· Eligibility to work in the United States required.
· Experience supporting CLIA/CAP accreditation, LDT development, or regulated laboratory environments preferred.
· Experience supporting clinical development programs in oncology or molecular diagnostics preferred.