Base: $151,500 to $252,500; bonus/equity: annual b...
Clinical diagnostic strategy implementation
Oncology clinical development
Clinical trial assay implementation
Drives the implementation of clinical diagnostic plans for therapeutic programs in early and late stage clinical development across Oncology, ensuring audit readiness
Job Summary
Drives the implementation of clinical diagnostic plans for therapeutic programs in early and late stage clinical development across Oncology, ensuring audit readiness.
Accountable for the development of the clinical study’s diagnostics biosample collection, processing and storage strategies and ensuring their logistical feasibility and cost effectiveness.
The US salary ranges take into account a number of factors including work location within the US market, the candidate’s skills, experience, education level and the market rate for the role.
Matching Summary
Drives the implementation of clinical diagnostic plans for therapeutic programs in early and late stage clinical development across Oncology, ensuring audit readiness.
Salary
Base: $151,500 to $252,500; Bonus/Equity: annual bonus and eligibility to participate in our share based long term incentive program; Benefits: health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave
Skills & Requirements
Must-have
clinical diagnostic strategy implementation
Oncology clinical development
clinical trial assay implementation
Human Biological Sample management
vendor and partner management
diagnostic assay development and validation
Nice-to-have
scenario planning
matrix management
line management
global diagnostic regulatory requirements
Key Requirements
Bachelor’s degree in biological sciences
7+ years of industry experience
Experience in clinical trial specimen management
Experience overseeing third‑party vendors
Professional experience within Oncology therapeutic area