Associate Director, Data Management

Scorpion Therapeutics; United States; Remote; USD 140,000 - 190,000; Full time

Job summary

Scorpion Therapeutics is seeking an Associate Director of Data Management to oversee clinical trial data quality and integrity in biopharma development, with a focus on rare disease programs and regulatory compliance.

You will lead start-up and execution of trials with CROs and internal teams, develop data management timelines, review data for discrepancies, and drive audits and inspections while guiding cross-functional teams in data-related activities.

Qualifications

• Bachelor's in life sciences or related field required.
• 8+ years of data management experience, including vendor management and EDC proficiency.
• Knowledge of clinical data standards (CDASH, SDTM) preferred.

Responsibilities

• Lead start-up and execution of trials with CROs and internal teams.
• Develop and manage data management timelines.
• Perform data review and discrepancy resolution.
• Lead audits and inspections.
• Guide cross-functional teams in data-related activities.

Skills

Data management

Vendor management

Cross-functional work

Education

Bachelor's in life sciences or related field

Tools

Medidata RAVE

EDC systems

Job description

Role:

Associate Director, Data Management overseeing clinical trial data quality and integrity within biopharma development, primarily in rare disease programs, with a focus on regulatory compliance and process improvements.

Responsibilities:

• lead start-up and execution of trials in collaboration with CROs and internal teams
• develop and manage data management timelines
• perform data review and discrepancy resolution
• lead audits and inspections
• guide cross-functional teams in data-related activities

Qualifications:

• Bachelor's in life sciences or related field
• 8+ years of data management experience, including vendor management and EDC systems proficiency (preferably Medidata RAVE)

HighValue:

extensive experience with clinical data standards (CDASH, SDTM), managing outsourced studies, GxP, ICH/GCP guidelines, and knowledge of coding dictionaries (MedDRA, WHODrug).

Collaboration:

work closely with clinical trial teams, vendors, and internal departments; reports to senior leadership.

Work setup:

Remote in San Diego with approximately 10% travel.