Manager, Clinical Biomarker Operations

Scorpion Therapeutics; California (MO); Presencial; USD 143 000 - 178 000; Tempo integral

Resumo da oferta

Scorpion Therapeutics is seeking a Manager, Biospecimen Operations in Translational Medicine to lead end-to-end biomarker activities for phase III oncology trials. You will manage sample lifecycle, vendor coordination, and central lab startup, driving operational excellence.

The role requires BS/MS in life sciences with 7+ years in clinical research or diagnostic labs, plus experience in biomarker/CDx operations and NGS methods. Onsite in Redwood City, CA with travel opportunities.

Qualificações

• BS/MS in life sciences.
• 7+ years in clinical research or diagnostic labs.
• Experience in biomarker and CDx operations, especially in phase 1–3 oncology trials.
• Proficiency in sample management systems and NGS methods.
• Strong communication, planning, and multitasking skills.

Responsabilidades

• Oversee end-to-end biomarker activities including protocol review, sample lifecycle management, vendor coordination, central lab startup, and operational process optimization.
• Collaborate with cross-functional teams (Biomarker Leads, Clinical Ops, Data Management).
• Support regulatory submissions and CDx filings.
• Manage vendor qualification and audits.
• Provide metrics and updates for senior leadership.

Conhecimentos

Biomarker operations

Clinical research experience

Sample management

Regulatory submissions

Communication skills

Project management

Formação académica

BS/MS in life sciences

Ferramentas

TruTech

SLOPE

LIMS

Descrição da oferta de emprego

Role

Manager, Biospecimen Operations within Translational Medicine, supporting phase III oncology trials with biomarker operational expertise.

Responsibilities

• oversee end-to-end biomarker activities including protocol review, sample lifecycle management, vendor coordination, central lab startup, and operational process optimization
• collaborate with cross-functional teams (Biomarker Leads, Clinical Ops, Data Management)
• support regulatory submissions and CDx filings
• manage vendor qualification and audits
• provide metrics and updates for senior leadership

Requirements

• BS/MS in life sciences
• 7+ years in clinical research or diagnostic labs
• experience in biomarker and CDx operations, especially in phase 1–3 oncology trials
• proficiency in sample management systems (e.g., TruTech, SLOPE, LIMS) and NGS methods
• strong communication, planning, and multitasking skills
• Preferred: experience with Project Management tools, LIMS, and NGS for RAS mutation analysis

High-Value

oncology, phase 1-3 trials, biomarker/CDx operations, regulatory submissions, central laboratory oversight, real-time sample tracking, cross-functional collaboration.

WorkSetup

based in Redwood City, CA; salary range $143,000–$178,000 USD; onsite with possible travel.