About this role
Role Overview
- Lead and develop a team of Clinical Laboratory Study managers (CLSM) for various therapeutic areas including Immuno-Oncology (IO)
- Key driver of precision medicine operational execution partnering with various teams to deliver high-quality samples and data
- Participate in cross-functional study teams and sub-teams across clinical and research departments
- Works with project manager and set-up manager of central/specialty lab and clinical study team to build lab database to address clinical trial sample collection needs, kits, testing and logistics
- Monitor acquisition of clinical trial samples and ensure compliance with ICF permissions
- Supports clinical study teams for technical and operational sample-related matters
- Manages FSP CLSM team for technical and operational support on their assigned therapeutic program and studies.
Requirements
- Bachelors degree
- Minimum of 8 years pharmaceutical experience in matrix interaction preferably in a pharmaceutical or biotech industry, or in academic or governmental cross-disciplinary teams
- Minimum of 5 years’ experience with Clinical Trials, focus on clinical sample collection.
- Extensive experience in Clinical laboratory operations, biospecimen logistics, and/or clinical study experience requested.
- Strong understanding of technical, clinical, and strategic aspects of laboratory operations delivery required.
- Clinical study knowledge, demonstrated by knowledge in science and technology.
- Demonstrated experience in stake holder management, leading internal and external meetings and solutioning skills.
Benefits
- health and wellness programs (including medical, dental, vision, life, and disability insurance)
- fitness centers
- 401(k) company match
- family support benefits
- equity awards
- annual bonuses
- paid time off
- paid leaves (e.g., military and parental leave)