Director, Clinical Data Management

Scorpion Therapeutics; California (MO); On-site; USD 211,000 - 264,000; Full time

Job summary

Scorpion Therapeutics in Redwood City, CA seeks a Director of Clinical Data Management to lead CDM tasks, ensure data quality and regulatory compliance, and oversee vendor relationships with CROs.

You will review CRFs, manage EDC systems, and drive Data Management Plans across early- and late-stage oncology trials, bringing 15+ years of trial experience and strong leadership in a fast-paced, high-energy environment.

Qualifications

• 15+ years of experience designing and executing clinical trials.
• Strong knowledge of clinical data standards and regulatory guidelines.
• Experience with data integrity, GxP, FDA/ICH compliance.
• Leadership experience in clinical data management.

Responsibilities

• Manage CDM tasks and vendor oversight across trials.
• Ensure data quality, accuracy, and regulatory compliance.
• Collaborate with CROs and cross-functional teams on CRFs and data flows.
• Oversee EDC systems and adherence to Data Management Plans.

Skills

CDM leadership

Regulatory knowledge

Vendor management

Education

MS or BS/BA or equivalent

Tools

EDC systems

Job description

Role: Director of Clinical Data Management at a biopharma oncology company focusing on RAS inhibitors

Core responsibilities include managing CDM tasks, vendor oversight, and ensuring data quality, accuracy, and compliance with GxP, FDA, and ICH guidelines. The role involves collaboration with CROs, data vendors, and cross-functional teams, including review and development of CRFs, management of EDC systems, and adherence to Data Management Plans.

Requirements:

• MS, BS/BA or relevant qualification;
• 15+ years of experience in designing and executing clinical trials, with strong knowledge of clinical data standards, medical coding, and regulatory guidelines.

Preferred:

• Oncology experience, especially in solid tumors, and 5+ years of line management.
• High-value specifics include expertise in early and late-stage trials, clinical database management, and a leadership role in a high-energy, innovative environment.

The position is based at headquarters in Redwood City, CA, with a salary range of $211,000–$264,000, and involves stakeholder management, regulatory compliance, and process development.