Lead Data Manager
Madrigal Pharmaceuticals · Conshohocken, PA · 2 wk ago
Information Technology$144k–$176k/yrFull-time
Key Responsibilities
- Serve as the Data Management lead for one or more clinical studies, accountable for end-to-end data management activities from study start-up through database lock.
- Develop and maintain study-level Data Management Plans (DMPs), CRF completion guidelines, edit check specifications, and other data management documentation.
- Lead EDC system setup, user acceptance testing (UAT), and database change control in collaboration with vendors and internal teams.
- Cover ongoing data review, query management, and data cleaning activities to ensure data integrity and completeness.
- Oversee external data handling, including laboratory, ECG, imaging, PK/PD, and ePRO integrations, ensuring timely reconciliation and issue resolution.
- Monitor study progress, track data metrics, and proactively identify and address data-related risks and delays.
- Lead database lock planning and execution, including review of data listings and coordination of cross-functional deliverables.
- Serve as the primary point of contact for CROs, EDC vendors, and functional partners for assigned studies.
- Ensure compliance with Madrigal SOPs, GCP, ICH, and regulatory requirements in all data management activities.
- Contribute to process improvement initiatives and provide input on departmental tools, templates, and standards.
- May provide training, mentoring, and oversight to junior data management staff.
Qualifications And Experience
- Bachelor’s degree in Life Sciences, Computer Science, or related field.
- Minimum of 5–7 years of experience in clinical data management within the pharmaceutical or biotechnology industry, including study-level lead experience.
- Demonstrated proficiency with EDC systems such as Medidata Rave, Oracle InForm, or Veeva CDMS.
- Strong understanding of clinical data standards (CDASH, SDTM) and data integration practices.
- Working knowledge of ICH GCP, FDA, and other regulatory guidelines relevant to clinical research.
- Prominent ability to manage vendor deliverables, timelines, and budgets.
- Excellent organizational, analytical, and problem-solving skills.
- Strong written and verbal communication skills with experience presenting data management deliverables cross-functionally.
- Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook).