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Clinical Research Coordinator

Company: Medix---
Location: Fall River
Posted on: May 14, 2022

Job Description:

We are looking for a Study Coordinator with a minimum of 2-3 years in Clinical Research for a full time hybrid role. This is a long term contract position, and sponsorship will not be offered at this time.

Responsibilities
Reviews and develops a familiarity with protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality, privacy protections.
Determine the eligibility of study participants according to protocol guidelines.
Registers new patients onto studies in a timely manner.
Registers each participant in the billing matrix to ensure billing of study procedures to the appropriate funding source.
Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
Collects, spins, separates and prepares specimens when needed; ships requested specimens in a timely manner.
Collects and submits tumor tissue samples and pathology slides as required.
Provides in-service education and on-going communication to CRC peers and collaborating institutions with study updates.
Reviews medical records, enters, and tracks all patient data into the appropriate data collection systems.
Completes study documentation and maintains study files in accordance with COG, other consortium, or industry requirements and University policies and procedures including, but not limited to, consent forms, source documentation, narrative notes if applicable, case report forms, and investigational material accountability forms.
Works with the Regulatory Coordinator to submit all protocol modifications, amendments, and renewals to COG, NCI, the IRB, and Cancer Center within the required timelines
Prepares all materials for both institutional and cooperative group audits.
All other duties as assigned

Keywords: Medix---, Fall River , Clinical Research Coordinator, Healthcare , Fall River, Massachusetts

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