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

Memorial Healthcare

5d•Onsite

About The Position

At Memorial, we are dedicated to improving the health, well-being and, most of all, quality of life for the people entrusted to our care. An unwavering commitment to our service vision is what makes the difference. It is the foundation of The Memorial Experience. Summary: Coordinates and assists with the implementation of multiple clinical research studies. Candidates with Oncology Regulatory clinical research experience highly preferred.

Requirements

High School Diploma or Equivalent (Required)
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.
Two (2) years of clinical research experience required.

Nice To Haves

Candidates with Oncology Regulatory clinical research experience highly preferred.

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.