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Part-Time Principal DM II

PharPoint Research • Durham, NC, US • published 2026-09-29 08:55:30.954339

Description

Description: **\*\*\*\*\* This is a part\-time, hybrid role based in either our Durham, NC or Wilmington, NC office \*\*\*\*\*\*** **BASIC SUMMARY:** Manage the technical and administrative development and execution of the data management functions of clinical trials for multiple and complex projects. Execute data management functions in accordance with Good Clinical Practice (GCP) and Standard Operating Procedures (SOPs). **ESSENTIAL DUTIES AND RESPONSIBILITIES:** * Manage and work concurrently on multiple protocols. * Manage coding activities involved with developing and maintaining a clinical trials database for analysis and/or transfer to sponsor. * Create case report forms (CRFs) and/or maintain oversight responsibility for CRF design in accordance with the protocol and established standards. * Develop project specific data management plans (DMPs) and other related documentation. * Review reports, listings, and other documents generated in data management for distribution to sponsor, investigators and their study support staff. * Design, validate, implement, and maintain projects in any clinical data management system used by the company. * Serve as the primary project contact...

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