Director, Clinical Operations

Scorpion Therapeutics; Watertown (MA); Hybrid; USD 160,000 - 230,000; Full time

Job summary

Scorpion Therapeutics seeks a Director of Clinical Operations to lead global Phase 2/3 hematology trials in a biopharma setting. You will oversee study execution, manage trial managers and vendors, and shape clinical strategies while ensuring GCP/ICH compliance.

The role requires 10+ years in trial management within biotech, pharma, or CROs, with strong leadership and communication skills and willingness to travel domestically and internationally. Hybrid work in Watertown, MA.

Qualifications

• BA/BS and 10+ years of trial management experience in biotech, pharma, or CROs.
• Deep knowledge of clinical development, GCP, and global regulations.
• Experience with electronic data capture (EDC) systems.
• Strong leadership and communication skills; ability to travel domestically and internationally.

Responsibilities

• Oversee global Phase 2/3 trials and study execution.
• Manage trial managers and vendors.
• Develop and implement clinical strategies.
• Ensure compliance with GCP/ICH and regulatory standards.
• Track KPIs to ensure timely delivery.
• Collaborate with medical, regulatory, data, and biometrics teams.
• Contribute to regulatory documentation and optimize study processes.

Skills

Trial management

GCP/ICH knowledge

Leadership

Regulatory knowledge

Communication skills

Travel willingness

Education

Bachelor's degree

Tools

EDC systems

Job description

Role

Director of Clinical Operations leading global Phase 2/3 clinical trials in a biopharma setting focused on hematologic diseases.

Responsibilities

oversee study execution, manage trial managers and vendors, develop and implement clinical strategies, ensure compliance with GCP/ICH and regulatory standards, and track KPIs for timely delivery. Collaborate with medical, regulatory, data, and biometrics teams; contribute to regulatory documentation; and optimize study processes.

Requirements

BA/BS, 10+ years of trial management experience within biotech, pharma, or CROs; strong knowledge of clinical development processes, GCP, and global regulations; proficiency in electronic data systems; leadership and communication skills; willingness to travel domestically and internationally.

Preferred

experience in orphan indications or oncology.

High-Value

leading Phase 2/3 hematology trials, global study oversight, vendor management, and cross-functional collaboration.

Work setup

hybrid in Watertown, MA, with travel.