Psicro

Clinical Study Coordinator

Cleveland, Tennessee, United States

Sponsorship not specifiedDetected 36 days ago

GCPSEOLogisticsClinical TrialsClinical ResearchResearchCommunicationCollaborationTime ManagementMentoringGxP

About the role

Milestone One is a Site Enabling Services organization with global headquarters in Zug, Switzerland.
Protocol-specific tasks will be determined by the Principal Investigator, considering all local and federal laws and regulations and upon review of competencies observed and documented by Milestone One.
In addition, mentoring staff and administrative tasks as assigned by the Milestone One Manager.

Facilitates the evaluation of proposed studies and ensures responses to feasibility questions are provided in due time.
Actively participates in patient recruitment/identification and evaluation for study inclusion by confirming eligibility according to the Inclusion and exclusion criteria.
Assists with plan development for new recruitment / retention tools, source documentation and other site tools to enhance quality and time management of research staff.
Assists the local research team in obtaining informed consent before study entry or any study-related procedures or tests being performed.
Assist with obtaining the required assessments at each visit per the protocol and notify the investigator of any critical values that need immediate attention or would prohibit or delay study treatment.
Assist with obtaining local and central laboratory testing, processing, and shipping per site SOP and study-specific lab manual.
Provides regular updates to the staff and investigators regarding study amendments.
Protocol and sponsor/CRO guidance will be followed if a study participant requires unblinding.

The Site/Study Coordinator supports a medical institution in clinical trial-related activities.

We understand what clinical study sites need and our overall mission is to support sites in stronger study delivery.

, general study conduct tasks, assistance with data entry into study related EDC systems, contact with CRO or sponsor representatives to schedule and conduct monitoring visits as well as resolve study specific issues at

This listing is sourced directly from Psicro's careers page and normalized into a canonical job model.