Oncology Regulatory Research Coordinator II - FT - Days - MCI Clinical Research
Memorial Healthcare•Pembroke Pines, FL
•Onsite
About The Position
Coordinates and assists with the implementation of multiple clinical research studies. Candidates with Oncology Regulatory clinical research experience highly preferred. This role 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.
Requirements
- High School Diploma or Equivalent (Required)
- Two (2) years of clinical research experience required.
- Oncology Regulatory clinical research experience highly preferred.
Nice To Haves
- Candidates with Oncology Regulatory clinical research experience highly preferred.
Responsibilities
- Assists in training/mentoring of CRC I and other team members as required
- Processes and ships research specimens per protocol guidelines.
- 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.
- 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.
- Manages the handling of adverse events, compliance and other participant-related issues.
- Handles resolution of data queries with sponsor.
- Responsible for training and educating staff.
- Coordinates the preparation and delivery of departmental communications, presentations and marketing/educational materials.
Benefits
- Veteran’s Preference
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED
