Clinical Data Coordinator

Madrigal Pharmaceuticals•Conshohocken, PA

9d•$73,200 - $89,500•Hybrid

About The Position

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. This role works closely with Data Managers, Clinical Operations, Biostatistics, and external vendors to facilitate accurate and timely database delivery for Madrigal Pharmaceuticals’ clinical development programs. The Clinical Data Coordinator contributes to data entry tracking, query management, and data cleaning activities in alignment with Good Clinical Practice (GCP) and company standards.

Requirements

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.

Nice To Haves

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.

Responsibilities

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.