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Medasource · 12 hours ago

Clinical Research Coordinator

SLC Metro Area

Contract

Onsite

New Grad, Entry Level

$30/hr - $30/hr

Medasource is a company focused on clinical research, and they are seeking a Clinical Research Coordinator to manage multiple research protocols. The role involves liaising with local investigators and sponsors while ensuring compliance with research operations and regulations.

Health CareMedical

Growth Opportunities

Responsibilities

Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement

During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date

Performs routine operational activities for multiple research protocols

Liaise between site research personnel, industry sponsors, and Supervisor

Collaborates closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable

Coordinates schedule of assessments from initial submission of feasibility until study closeout

Reviews the study design and inclusion/exclusion criteria with physician and patient

Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements

Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data

Creates study specific tools for source documentation when not provided by sponsor

Collects, completes, and enters data into study specific case report forms or electronic data capture systems

Generates and tracks drug shipments, device shipments, and supplies as needed

Ensures timely and accurate data completion

Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations

Communicates all protocol-related issues to appropriate study personnel or manager

Attends study specific on-site meetings, investigator meetings, conference calls and monthly CRC meetings, as required

Reviews and responds to any monitoring and auditing findings

Qualification

Clinical research protocolsData collection toolsInformed consent proceduresAdverse event trackingCommunication skills

Required

Responsible for Coordinating multiple research protocols and serving as a liaison with local investigators and Sponsors

Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a fundamental understanding of human subject research

Practice and adhere to the 'Code of Conduct' philosophy and 'Mission and Value Statement'