Senior Clinical Data Manager – Lead for Trials

Madrigal Pharmaceuticals

Conshohocken (Montgomery County)

On-site

USD 129,600 - 158,400

Full time

14 days+
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Benefits offered by this job

Equity
Flexible PTO
Medical, dental, vision, life/disabilt
401(k)

Job summary

Madrigal Pharmaceuticals is seeking a Lead Data Manager to oversee data management for assigned clinical studies, ensuring high-quality, regulatory-compliant trial data. This role serves as the primary DM contact across cross-functional teams and vendors.

You will lead EDC setup and change control, develop DM Plans, monitor data quality, coordinate database locks, and drive process improvements within R&D. Requires 5–7 years in clinical data management, experience with Medidata Rave/Oracle

Qualifications

  • Bachelor's degree in Life Sciences, Computer Science, or related field.
  • 5–7 years of clinical data management experience, including lead responsibilities.
  • Proficiency with EDC systems (Medidata Rave, Oracle InForm, Veeva CDMS).
  • Strong knowledge of CDASH/SDTM and regulatory guidelines (ICH GCP, FDA).
  • Experience managing vendors, timelines, and budgets.

Responsibilities

  • Lead data management for one or more clinical studies from start-up to database lock.
  • Develop and maintain study-level Data Management Plans (DMPs) and CRF guidelines.
  • Oversee EDC system setup, UAT, and change control with vendors and internal teams.
  • Coordinate data review, query management, and data cleaning to ensure data integrity.

Skills

Leadership
Data management
Vendor management
EDC systems
Regulatory knowledge

Education

Bachelor's degree in Life Sciences, Computer Science, or related field

Tools

Medidata Rave
Oracle InForm
Veeva CDMS

Job description

Madrigal Pharmaceuticals is seeking a Lead Data Manager to oversee data management for assigned clinical studies, ensuring high-quality, regulatory-compliant trial data. This role serves as the primary DM contact across cross-functional teams and vendors.

You will lead EDC setup and change control, develop DM Plans, monitor data quality, coordinate database locks, and drive process improvements within R&D. Requires 5–7 years in clinical data management, experience with Medidata Rave/Oracle

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