Senior Manager, Clinical Data Management
Corcept Therapeutics
August 15, 2026
On-site
Redwood City, CA
Clinical Research and Development
Responsibilities:
- Provide input into the design of data flow across EDC and non-EDC data sources across vendor network
- Manage data management service providers to ensure quality of deliverables and timelines are met
- Develop and contribute to processes enabling near-real-time data access for clinical trials
- Ensure data quality through implementation of CDISC compliance
- Review and assess data query resolution metrics; suggest process improvements
- Review study protocols to ensure data collection and CRF design meet study objectives
- Manage and oversee SAE and external vendor reconciliation between clinical and applicable databases
- Review clinical data for completeness, accuracy, and consistency
- Provide subject matter expertise to project team members throughout the project lifecycle
- Provide accurate and timely clinical data to internal and external customers upon request
- Manage development, testing, and maintenance of data management systems
- Support development and periodic review of Data Management SOPs, WIs, and templates
- Provide subject matter expertise for internal/external audits and inspections
- Maintain compliance with company and study-specific learning requirements
Preferred Skills/Qualifications/Technical Proficiencies:
- Relational databases, SAS, and clinical data management systems
- Knowledge of CDISC/SDTM (hands-on preferred)
- Hands-on experience with mainstream EDC systems (e.g., Rave, Medrio)
- Data visualization tools familiarity (e.g., Tableau, RShiny) a plus
- Regulatory guidelines: ICH, GCDMP, 21 CFR Part 11
- Strong management abilities for project/staff management of data management deliverables
Preferred Education/Experience:
- Bachelor’s or higher in science, math, or computer science
- 5+ years’ clinical data management experience (med device, pharma, or biotech)
- Experience in IT-related field
- Experience with oncology or rare disease clinical trials and CDISC therapeutic area standards
- Experience managing data flow and curating biomarker data
- Experience managing Data Management CROs and vendors
Application instructions:
- Applicants must be currently authorized to work in the United States on a full-time basis.
- Provide input into the design of data flow across EDC and non-EDC data sources across vendor network
- Manage data management service providers to ensure quality of deliverables and timelines are met
- Develop and contribute to processes enabling near-real-time data access for clinical trials
- Ensure data quality through implementation of CDISC compliance
- Review and assess data query resolution metrics; suggest process improvements
- Review study protocols to ensure data collection and CRF design meet study objectives
- Manage and oversee SAE and external vendor reconciliation between clinical and applicable databases
- Review clinical data for completeness, accuracy, and consistency
- Provide subject matter expertise to project team members throughout the project lifecycle
- Provide accurate and timely clinical data to internal and external customers upon request
- Manage development, testing, and maintenance of data management systems
- Support development and periodic review of Data Management SOPs, WIs, and templates
- Provide subject matter expertise for internal/external audits and inspections
- Maintain compliance with company and study-specific learning requirements
Preferred Skills/Qualifications/Technical Proficiencies:
- Relational databases, SAS, and clinical data management systems
- Knowledge of CDISC/SDTM (hands-on preferred)
- Hands-on experience with mainstream EDC systems (e.g., Rave, Medrio)
- Data visualization tools familiarity (e.g., Tableau, RShiny) a plus
- Regulatory guidelines: ICH, GCDMP, 21 CFR Part 11
- Strong management abilities for project/staff management of data management deliverables
Preferred Education/Experience:
- Bachelor’s or higher in science, math, or computer science
- 5+ years’ clinical data management experience (med device, pharma, or biotech)
- Experience in IT-related field
- Experience with oncology or rare disease clinical trials and CDISC therapeutic area standards
- Experience managing data flow and curating biomarker data
- Experience managing Data Management CROs and vendors
Application instructions:
- Applicants must be currently authorized to work in the United States on a full-time basis.