Clinical Trial Manager (CTM)

Scorpion Therapeutics; Brisbane (CA); On-site; USD 140,000 - 210,000; Full time

Job summary

Scorpion Therapeutics seeks a Senior Clinical Trial Manager to lead end-to-end management of assigned clinical trials in biopharma, focusing on drug development processes. You will oversee trial operations, manage CRO/vendor relationships, and ensure adherence to GCP, FDA, EMA, and ICH guidelines.

Collaborating with Data Management on CRFs and data deliverables, you will coordinate with study teams, site investigators, and stakeholders; monitor enrollment, trial progress, and budgets; and

Qualifications

• Must have strong understanding of regulatory guidelines (GCP, FDA, EMA, ICH).
• Excellent communication, organization, and problem-solving skills.
• Willingness and ability to travel ~25% to sites and meetings.

Responsibilities

• Oversee end-to-end trial operations and lifecycle management.
• Manage CRO/vendor relationships and ensure contract compliance.
• Collaborate with Data Management on CRFs and data deliverables; coordinate with study teams and investigators.
• Monitor enrollment, progress, and budgets; drive risk mitigation and issue resolution.
• Prepare for audits and inspections; ensure regulatory readiness and documentation.

Skills

Regulatory knowledge

Communication

Project coordination

Travel readiness

Education

Bachelor's degree in biological sciences

Job description

Role

Senior Clinical Trial Manager responsible for end-to-end management of assigned clinical trials in biopharma, with a focus on drug development processes.

Responsibilities

• oversee trial operations, manage CRO/vendor relationships, ensure compliance with GCP, FDA, EMA, and ICH regulations;
• collaborate with Data Management on CRFs and data deliverables;
• coordinate with study teams, site investigators, and stakeholders;
• monitor enrollment, trial progress, and budgets;
• prepare for audits and inspections;
• identify risks and implement solutions.

Requirements

• B.S. in biological sciences or related field;
• 5+ years of industry experience managing clinical trials independently;
• strong knowledge of regulatory guidelines;
• excellent communication, organization, and problem-solving skills;
• ability to travel (~25%).

Preferred

• experience in oncology, immunology, or inflammatory diseases;
• familiarity with targeted protein degradation modalities;
• experience in early-phase (Ph1-3) trials.

HighValue

full trial lifecycle ownership, vendor management, regulatory compliance, and cross-functional team leadership in a fast-paced, innovative biopharma environment.

Work Setup

onsite in Brisbane, CA; travel required.