Senior Clinical Trial Assistant Jobs

5+ years previous clinical research experience in clinical trial coordination, site management, and or vendor management.

Must have the ability to build and maintain positive relationships with management and peers

Manage the collection, review and approval of regulatory documents from clinical sites

Manages and tracks study specific payments

Manage ancillary vendors, such as a specialty lab

Review site visit reports, under the direction of the Clinical Program Manager or designee

Directly support under the guidance of Operational Leaders, Clinical Leaders, and Clinical Trial Managers. Specific responsibilities include:

Maintain and manage requests for access to and deactivation of study systems users.

Competency of the drug development process with knowledge of ICH-GCP is a plus

Strong interpersonal, organizational and planning skills along with excellent verbal and written communication skills

Distribute safety alerts and relevant documents, if required

Maintain and update study team and vendor contact information