Director, Clinical Data Management

Role Summary

Director of Clinical Data Management reporting to the Sr. Director, Clinical Data Management. You will be responsible for all data processes related to assigned studies, overseeing data collection workflows across all data sources, ensuring the quality and integrity of all clinical data including CRF and edit check specifications, Data Management Plans, data systems validation and UAT, listings generation, and ensuring review of clinical data for completeness, accuracy, and compliance.

This role is based out of either our San Francisco, CA or Cambridge, MA office.

Responsibilities

• Day-to-day management of vendors involved in data management, to ensure quality of deliverables and that SET timelines are met
• Gather input from stakeholders and design data flow across data sources and across vendors
• Develop and review study plans and protocols to ensure that data collection designs meet study objectives (i.e., System Validation Plans, Data Management Plans, Data Transfer Plans, Data Review Plans, Data Monitoring Plans, and Data Coding Guidelines)
• Develop and review specifications for database build and validation, edit checks, external system integration, or other systems and processes related to data while enabling near-real time data access for Olema clinical trials
• Ensure quality of clinical data by review for completeness, accuracy and consistency in accordance with study plans
• Support SAE reconciliation between clinical and pharmacovigilance databases and external data reconciliation within the clinical database
• Provide Clinical Data Management subject matter expertise to study team members during all phases of the project life cycle, including internal and external audits and inspections
• Lead a team of data management professionals
• Assist in the development and periodic review of Data Management specific SOPs, WIs, and templates while assessing metrics and implementing suggested improvements

Qualifications

• Required: Bachelor’s degree or higher in science, biology, mathematics or computer science
• Preferred: CCDM certification
• Required: Experience across early to late-phase clinical trials; late-phase oncology experience required
• Preferred: Practical knowledge of MedDRA, WHODrug and/or another controlled thesaurus
• Preferred: Knowledge of Project Management Principles; a PMP certification is a plus
• Preferred: Deep expertise in Excel and MS Office tools
• Preferred: Relational database understanding and SQL knowledge
• Preferred: Understanding of data manipulation, for example using SAS, R, or Python/Pandas
• Required: 15+ years of experience in data management in the clinical trial industry (med device, pharma or biotech)
• Required: At least 5 years of experience managing data management professionals
• Required: In-depth understanding of clinical and data management regulations and guidelines: ICH, GCDMP, 21CFR Part 11, GDPR; functional knowledge of CDISC/SDTM/SDTMIG standards
• Required: Experience managing data management CROs
• Required: Deep experience in reviewing clinical data
• Required: Hands-on deep experience working with EDC systems (e.g., Rave, Veeva)
• Preferred: Data visualization tools (Spotfire, Tableau, RShiny, Dash)
• Preferred: Experience with management of data flow and curation of biomarker data
• Preferred: Experience with a programming language

Education

• Bachelor’s degree or higher in science, biology, mathematics or computer science
• CCDM certification preferred

Additional Requirements

• 5% travel