Clinical Trial Manager II

Scorpion Therapeutics; Princeton (NJ); On-site; USD 120,000 - 160,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Trial Manager 2 to oversee global phase 2/3 oncology studies, including NSCLC and colorectal cancer trials with ivonescimab. You will manage site selection, feasibility, enrollment, monitoring, and closeout, collaborating with CROs to ensure data quality and regulatory compliance.

The role requires 6+ years in international trial management, strong GCP/ICH knowledge, and travel up to 20%.

Qualifications

• Bachelor's in life sciences or related field.
• 6+ years in international clinical trial management within pharma/biotech, with 5+ years managing phase II/III oncology trials.
• Strong understanding of GCP, ICH guidelines, and drug development processes.
• Ability to travel up to 20%.

Responsibilities

• Manage site selection, feasibility, enrollment, monitoring, and closeout.
• Partner with CROs for trial execution, data quality, and compliance.
• Develop and review trial documentation (e.g., ICFs, CRFs, plans).
• Oversee site performance, risk management, and regulatory adherence.
• Mentor team members and ensure inspection readiness.

Skills

International clinical trial mgmt

Oncology trials

Phase II/III oversight

GCP/ICH knowledge

Travel flexibility 20%

Education

Bachelor's degree in life sciences

Job description

Role: Clinical Trial Manager 2 overseeing global phase 2/3 oncology studies, including NSCLC and colorectal cancer trials with ivonescimab.

Responsibilities

• manage site selection, feasibility, enrollment, monitoring, and closeout
• partner with CROs for trial execution, data quality, and compliance
• develop and review trial documentation (e.g., ICFs, CRFs, plans)
• oversee site performance, risk management, and regulatory adherence
• mentor team members and ensure inspection readiness

Requirements

• Bachelor's in life sciences or related field
• 6+ years in international clinical trial management within pharma/biotech, with 5+ years managing phase II/III oncology trials
• strong understanding of GCP, ICH guidelines, and drug development processes
• ability to travel up to 20%

High Value

• Oncology (NSCLC, CRC)
• Phase 2/3
• global trial oversight
• CRO collaboration
• regulatory compliance
• GCP expertise
• experience in biologics or targeted therapies

Work Setup

• Travel as needed
• based in a flexible or international setting