Oncology Regulatory Research Coordinator II - FT - Days - Office of Human Research jobs in United States
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Memorial Healthcare System · 3 days ago

Oncology Regulatory Research Coordinator II - FT - Days - Office of Human Research

Memorial Healthcare System is dedicated to improving health and quality of life. They are seeking an Oncology Regulatory Research Coordinator II to coordinate and assist with the implementation of clinical research studies, ensuring compliance with regulations and standards.

Health Care

Responsibilities

Collaborates to ensure the compliance with local, state and federal regulations and standards
Assists with responding to and preparing for audits and participates in audits
Responsible for completing, organizing, and submitting Institutional Review Board (IRB) for phase 1 - 4 trials required by the sponsor
Conducts initiation, monitoring and close out visits with the sponsor
Processes and ships research specimens per protocol guidelines
Assists in training/mentoring of CRC I and other team members as required
Responsible for training and educating staff
Coordinates the preparation and delivery of departmental communications, presentations and marketing/educational materials
Manages the handling of adverse events, compliance and other participant-related issues
Handles resolution of data queries with sponsor

Qualification

Oncology Regulatory ExperienceClinical Research ExperienceEffective CommunicationCritical ThinkingCustomer ServiceMulti-taskingTeam Collaboration

Required

High School Diploma or Equivalent (Required)
Two (2) years of clinical research experience required
Candidates with Oncology Regulatory clinical research experience highly preferred
Collaborates to ensure the compliance with local, state and federal regulations and standards
Assists with responding to and preparing for audits and participates in audits
Responsible for completing, organizing, and submitting Institutional Review Board (IRB) for phase 1 - 4 trials required by the sponsor
Conducts initiation, monitoring and close out visits with the sponsor
Processes and ships research specimens per protocol guidelines
Assists in training/mentoring of CRC I and other team members as required
Responsible for training and educating staff
Coordinates the preparation and delivery of departmental communications, presentations and marketing/educational materials
Manages the handling of adverse events, compliance and other participant-related issues
Handles resolution of data queries with sponsor
Requires critical thinking skills, effective communication skills, decisive judgment and the ability to work with minimal supervision
Demonstrates ability to work effectively as a team member
Ability to multi-task

Company

Memorial Healthcare System

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Be at the heart of exceptional care.

Funding

Current Stage
Late Stage

Leadership Team

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Paul Gaden
Chief Executive Officer, Memorial Regional Hospital
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Rita Bunch
Chief Operating Officer, Memorial Regional Hospital
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