Senior Clinical Data Manager

Scorpion Therapeutics; Indiana (PA); On-site; USD 120,000 - 190,000; Full time

Job summary

Scorpion Therapeutics is seeking a Senior Clinical Data Manager to lead global data management for early-phase CNS programs, including orexin receptor targets. You will oversee data strategies, data systems (EDC, IRT, ePRO), and vendor relationships to ensure high-quality, compliant datasets for regulatory submissions.

The role requires 6+ years in clinical data management within pharma/biotech, expertise with CDISC/CDASH, and CRO oversight. Based in the US with occasional travel.

Qualifications

• Bachelor's or Master's degree in a related field.
• 6+ years of clinical data management experience in pharma/biotech.
• Expertise with CDISC/CDASH standards and regulatory requirements.
• Experience overseeing CRO/vendor relationships.

Responsibilities

• Lead global clinical data management activities.
• Develop and oversee data strategies for programs.
• Manage data systems (EDC, IRT, ePRO).
• Ensure CDISC/CDASH standards compliance.
• Oversee CRO/vendor collaborations.
• Support regulatory submissions.

Skills

Data management leadership

CDISC/CDASH

EDC platforms

Vendor oversight

Regulatory submissions

Education

Bachelor's or Master's degree

Tools

EDC software

ePRO systems

Job description

Role

Senior Clinical Data Manager supporting Centessa's neuro-focused early-phase programs, including orexin receptor 2 (OX2R) agonists for sleep disorders.

Responsibilities

• lead global clinical data management activities
• develop and oversee data strategies
• manage data systems (e.g., EDC, IRT, ePRO)
• ensure standards compliance (CDISC/CDASH)
• oversee CRO/vendor collaborations
• support regulatory submissions

Qualifications

• Bachelor's or Master’s degree
• 6+ years' clinical data management experience in pharma/biotech
• expert in clinical trial technologies
• experienced with CRO/vendor oversight
• familiar with regulatory requirements (Pre-IND to NDA/BLA)

Preferred

• experience in early-phase CNS or neurodegenerative trials
• supporting regulatory submissions

HighValue

• CNS/neuro indications
• early-phase (Ph1-3)
• global development
• electronic data systems
• CRO/vendor management
• regulatory support

WorkSetup

• based in the US
• with occasional travel