CDM Lead for Complex Clinical Studies

Scorpion Therapeutics; United States; On-site; USD 140,000 - 220,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Data Management (CDM) lead to oversee CDM execution at the project level for products or complex studies, including CRF/eCRF design, review of protocols, and vendor coordination.

You will mentor CROs and study teams on CDM requirements, support regulatory submissions, ensure data completeness and regulatory compliance, and drive CDM process improvements with vendors.

Qualifications

• PhD in life sciences/related; or MA/MS with 4+ years; BA/BS with 6+ years in CDM or data analytics/data management. Prefer PhD + 2+ years CDM/data management.
• Experience leading small projects/teams.

Responsibilities

• Act as CDM lead; oversee CDM execution at the project level (products or complex studies).
• Lead CRF/eCRF design; review study protocols and plan/implement CDM portions of clinical studies.
• Oversee vendors for data review, transfers and reporting; use routine/non-routine reports to track progress and meet timelines/quality.
• Guide/training for CROs, vendors, investigators and study coordinators on CDM requirements.
• Support regulatory submissions; assist with CDM questions for audits/inspections; lead special projects as needed.
• Oversee CDM process design/implementation with vendors (entry, QC, transfer, reporting, backup/recovery).
• Ensure data completeness/accuracy/consistency and adherence to CDM system processes for regulatory compliance.

Skills

CDM leadership

Regulatory knowledge

Project management

Mentoring

Communication

Education

PhD in life sciences/related

MA/MS with 4+ years in CDM

BA/BS with 6+ years in CDM

Job description

Scorpion Therapeutics is seeking a Clinical Data Management (CDM) lead to oversee CDM execution at the project level for products or complex studies, including CRF/eCRF design, review of protocols, and vendor coordination.

You will mentor CROs and study teams on CDM requirements, support regulatory submissions, ensure data completeness and regulatory compliance, and drive CDM process improvements with vendors.