Clinical Data Manager

Scorpion Therapeutics; San Diego (CA); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Scorpion Therapeutics is seeking a Clinical Data Manager to lead data management activities for clinical trials in a fast-paced environment in San Diego. You will oversee CRO data management teams, develop study documents, and ensure data integrity across the trial lifecycle.

Responsibilities include managing data collection and quality control, designing CRFs and EDC/IRT/ePRO systems, coordinating data transfers, and supporting database lock.

Qualifications

• Minimum 2 years of Clinical Data Management experience; 3+ years preferred.
• Bachelor's degree in a scientific or medical field is required.
• Proficiency in clinical data systems and data management processes.
• Strong analytical, communication, and multitasking skills.

Responsibilities

• Oversee CRO Data Management teams.
• Develop high-quality study documentation including Data Management Plans.
• Oversee data collection, handling and quality control; facilitate filing in TMF.
• Design and maintain CRFs and data entry systems (EDC, IRT, ePRO).
• Develop data review strategies and coordinate data transfers.
• Monitor data review processes and support timely database lock.
• Collaborate with Clinical Operations, Safety, and Biostatistics, as well as external vendors.
• Identify and upscale risks; ensure adherence to GxP, ICH, CDISC, FDA guidelines.

Skills

Clinical Data Management

Analytical skills

Communication skills

Multitasking

Clinical data systems

Education

Bachelor's degree in a scientific or medical field

Tools

EDC systems

IRT systems

ePRO systems

Job description

Role

Clinical Data Manager responsible for overseeing data management activities for clinical trials, ensuring compliance with industry standards, regulations, and SOPs.

Responsibilities

manage CRO Data Management teams, develop high-quality study documentation including Data Management Plans, oversee data collection, handling, and quality control; facilitate filing in TMF; design and maintain CRFs and data entry systems (EDC, IRT, ePRO); develop data review strategies, coordinate data transfers, monitor data review processes, and support timely database lock. Collaborate with Clinical Operations, Safety, and Biostatistics teams, as well as external vendors; identify and upscale risks; ensure adherence to GxP, ICH, CDISC, FDA guidelines.

Requirements

minimum 2 years of Clinical Data Management experience (preferably >3 years in the role), Bachelor's degree in a scientific or medical field, proficiency in clinical data systems, strong analytical, communication, and multitasking skills.

Preferred

experience in Phase 3 trials.

HighValue

clinical trial data management, GxP, CDISC, electronic data capture, cross-functional collaboration, regulatory compliance.

WorkSetup

not specified; likely office-based or hybrid based on typical industry standards.