Clinical Trial Manager (Oncology)

Scorpion Therapeutics; United States; Remote; USD 120,000 - 165,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Trial Manager to oversee the UTUC clinical trial from start-up to close-out, focusing on study execution, vendor oversight, and regulatory compliance.

The role involves managing CROs, study sites, protocol support, regulatory submissions, and study documentation, with periodic in-person collaboration and minimal travel.

Qualifications

• Bachelor's in life sciences
• 6-8 years clinical trial support experience including early phase and global trials
• 1-2 years CTM experience preferred
• Extensive knowledge of ICH/GCP and FDA regulations
• Proficiency with eTMF, CTMS, EDC
• Strong project management and communication skills

Responsibilities

• Oversee CROs, study vendors, and sites to ensure study execution
• Support protocol development, regulatory submissions, and study documentation
• Coordinate study activities and maintain audit readiness
• Track metrics and assist with budget management
• Travel limited to ~5-10% of time

Skills

Project management

Communication

Regulatory compliance

Education

Bachelor's in life sciences

Tools

eTMF

CTMS

EDC

Job description

Role: Clinical Trial Manager overseeing the UTUC clinical trial from start-up to close-out, focusing on study execution, vendor oversight, and regulatory compliance.

• manage CROs, study vendors, and sites
• support protocol development, regulatory submissions, and study documentation
• coordinate study activities, ensure audit readiness, and contribute to process improvements
• track metrics and support budget management
• minimal travel (~5-10%)

Requirements:

• Bachelor's in life sciences
• 6-8 years of clinical trial support experience, including early phase and global trials
• 1-2 years in a CTM role preferred
• extensive knowledge of ICH/GCP and FDA regulations
• proficiency with eTMF, CTMS, EDC
• strong project management and communication skills

HighValue:

• experience with early phase/registrational trials
• CRO/vendor management
• regulatory compliance
• electronic trial systems

WorkSetup:

• remote with periodic in-person collaboration