Madrigal Pharmaceuticals is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH). The Clinical Data Coordinator is responsible for supporting the collection, management, and quality assurance of clinical trial data to ensure data integrity and regulatory compliance.
Assist in the setup, maintenance, and closeout of clinical study databases across multiple phases of development
Support Data Managers in ensuring data accuracy, completeness, and consistency throughout the clinical trial lifecycle
Perform routine data entry checks, generate and track data queries, and ensure timely resolution in collaboration with site personnel and vendors
Participate in the review and testing of electronic data capture (EDC) systems, case report forms (CRFs), and data validation specifications
Track receipt and review of external data sources (e.g., laboratory, imaging, PK/PD, ECG, ePRO) to ensure timely integration and reconciliation
Assist in the preparation of Data Management Plans (DMPs), edit check specifications, and data validation listings
Maintain documentation of data cleaning activities, ensuring compliance with SOPs, GCP, and regulatory requirements
Participate in data review meetings and contribute to database lock readiness activities
Support audit and inspection preparation by ensuring documentation accuracy and traceability
Perform other related duties as assigned in support of departmental and corporate goals
Qualification
Required
Bachelor's degree in Life Sciences, Computer Science, or related field
Minimum of 1–2 years of experience in clinical data management or a related clinical research role within the pharmaceutical or biotechnology industry
Working knowledge of clinical trial processes and regulatory guidelines (GCP, ICH, FDA)
Experience with one or more electronic data capture (EDC) systems such as Medidata Rave, Oracle InForm, or Veeva CDMS
Proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook)
Strong attention to detail and organizational skills
Excellent written and verbal communication skills
Ability to work collaboratively in a hybrid team environment and manage multiple priorities
Preferred
Familiarity with clinical data standards (CDASH, SDTM) preferred
Exposure to complex or adaptive clinical trial designs
Experience supporting Phase II or III clinical trials
Familiarity with data from external vendors (e.g., central labs, imaging, ECG, ePRO, PK/PD)
Experience in oncology, metabolic, or cardiovascular clinical trials preferred
Prior involvement in data reconciliation, SAE reconciliation, or data review listings generation
Benefits
Equity offers meaningful opportunity allowing our employees to share in the success they help create
All full-time employees receive equity, which we believe reinforces our ownership culture
Comprehensive benefits, including flexible paid time off, medical, dental, vision and life/disability insurance, and 401(k) offerings (i.e., traditional, Roth, and employer match) in accordance with applicable plans
Additional voluntary benefits like supplemental life insurance, legal services, and other offerings
Mental health benefits through our Employee Assistance Program for employees and their family
Other benefits in accordance with applicable federal, state, and local laws
Madrigal Pharmaceuticals is a biopharmaceutical company developing therapeutics for the treatment of cardiovascular-metabolic diseases.
