Senior Clinical Data Management Lead – SDTM/CDISC

Scorpion Therapeutics; San Diego (CA); On-site; USD 131,000 - 179,000; Full time

Benefits offered by this job

Health benefits

Bonus program

Equity compensation

Retirement match

Paid time off

Job summary

Scorpion Therapeutics invites an experienced data management leader to oversee data activities across clinical studies and programs. You will design eCRFs, coordinate user acceptance testing, and ensure high-quality data for regulatory submissions.

The role requires strong supervisory experience, deep knowledge of CDISC/SDTM standards, and proficiency with Medidata Rave. Collaboration with Medical, Regulatory, and QA teams is essential.

Qualifications

• BS/BA in computer science or related field with 8+ years pharma experience.
• 3+ years supervisory/lead experience.
• Proficiency with Medidata Rave.
• Knowledge of CDISC/SDTM and FDA guidelines.

Responsibilities

• Leads, performs, and oversees data management activities for clinical studies and/or clinical programs.
• Performs hands-on clinical data management tasks: reviewing protocols, designing eCRFs, coordinating UAT, documenting edit check specs, QC’ing external data transfers, data quality checks/discrepancy review, and ensuring database lock activities.
• Develops policies, SOPs, processes, and documents for data management.
• Provides technical expertise and training within Data Management and related teams.

Skills

Data management

Leadership

Project management

Analytical

Communication

Education

BS/BA in computer science or related

MS in related field

PhD

Tools

Medidata Rave

SAS

Business Objects

Job description

Scorpion Therapeutics invites an experienced data management leader to oversee data activities across clinical studies and programs. You will design eCRFs, coordinate user acceptance testing, and ensure high-quality data for regulatory submissions.

The role requires strong supervisory experience, deep knowledge of CDISC/SDTM standards, and proficiency with Medidata Rave. Collaboration with Medical, Regulatory, and QA teams is essential.