Clinical Trial Manager

Scorpion Therapeutics; United States; Remote; USD 110,000 - 160,000; Full time

Job summary

Scorpion Therapeutics seeks a Clinical Trial Manager to oversee the operational execution of bladder cancer immunotherapy trials conducted with CG Oncology.

You will manage day-to-day trial activities, CRO/vendor oversight, site management support, start-up through closeout, and cross-functional collaboration, with domestic and international travel ~25%.

Qualifications

• Bachelor's degree in life sciences or health-related field.
• 5+ years in clinical research, with 2+ years in trial management or study leadership.
• Experience across all trial phases; global exposure preferred.
• Ability to travel about 25% domestically and internationally.
• Professional certification (ACRP or SOCRA) preferred.

Responsibilities

• Oversee day-to-day trial activities and timelines.
• Manage CRO/vendor performance and oversight.
• Support site management, data review, and risk mitigation.
• Coordinate start-up, conduct, and closeout activities.
• Ensure inspection readiness and regulatory compliance.
• Monitor budgets and study metrics.

Skills

Clinical trial management

CRO/vendor oversight

Budget monitoring

Study start-up/closeout

Regulatory compliance

Cross-functional collaboration

Education

Bachelor's in life sciences

Tools

CTMS

EDC

eTMF

Job description

Role

Clinical Trial Manager (CTM) overseeing operational execution of clinical trials in bladder cancer immunotherapy at CG Oncology.

Responsibilities

• manage day-to-day trial activities, oversee CRO/vendor performance, ensure compliance with timelines, quality, and regulations
• support site management, data review, risk mitigation, and study documentation
• coordinate study start-up, conduct, and closeout
• collaborate with cross-functional teams including Clinical Operations, Data Management, and Regulatory
• monitor budgets and study metrics
• ensure inspection readiness and quality standards

Qualifications

• Bachelor's in life sciences or health-related field
• 5+ years in clinical research, including 2+ in trial management or study leadership, preferably in oncology or sponsor-side environments
• experience supporting all trial phases, with global trial exposure preferred
• ability to travel ~25% domestically and internationally
• professional certification (e.g., ACRP, SOCRA) preferred

High-Value

Oncology (bladder cancer), immunotherapy, clinical trial management, study start-up to closeout, CRO/vendor oversight, remote work with travel.

Collaboration

works closely with the Clinical Project Manager and cross-functional teams.

Work setup

Fully remote, US-based with travel requirements.