Location
Fountain Valley, CA, United States
Posted
July 19, 2026
Job Description
Job Title: Source Document Specialist – Dermatology Clinical TrialsJob Description
The Source Document Specialist plays a key role in supporting dermatology industry-initiated clinical trials by developing, standardizing, and maintaining accurate source documentation. This position works closely with Clinical Research Coordinators and the Regulatory Coordinator to ensure that all study documents are complete, compliant, and inspection-ready in alignment with GCP, FDA regulations, and study protocols. The role is ideal for someone with clinical research experience who enjoys detail-oriented work, quality control, and collaborating within a high-volume, fast-paced research environment.
Responsibilities
+ Develop, create, and standardize source document templates based on study protocols and sponsor requirements.
+ Review study protocols, schedules of events, and case report forms (CRFs) to ensure source documents capture all required data points.
+ Mainta...
The Source Document Specialist plays a key role in supporting dermatology industry-initiated clinical trials by developing, standardizing, and maintaining accurate source documentation. This position works closely with Clinical Research Coordinators and the Regulatory Coordinator to ensure that all study documents are complete, compliant, and inspection-ready in alignment with GCP, FDA regulations, and study protocols. The role is ideal for someone with clinical research experience who enjoys detail-oriented work, quality control, and collaborating within a high-volume, fast-paced research environment.
Responsibilities
+ Develop, create, and standardize source document templates based on study protocols and sponsor requirements.
+ Review study protocols, schedules of events, and case report forms (CRFs) to ensure source documents capture all required data points.
+ Mainta...