Clinical Trial Coordinator

1 week ago

Newport Beach, United States Wake Research Full time
Job Overview

Company Overview:
M3 Wake Research, part of the M3USA network, is a leading organization specializing in clinical research, providing an extensive range of investigational services to global pharmaceutical, biotechnology, and medical device companies. With a robust network of research sites nationwide, we are recognized as one of the largest independent clinical research organizations in the United States.

Since our establishment in 1984, we have successfully conducted over 7,000 clinical trials, consistently delivering high-quality data and exceeding the expectations of our sponsors. Our proprietary database of potential clinical trial participants enables us to effectively match studies with qualified candidates.

Position Summary:
The Clinical Research Coordinator (CRC) plays a vital role in the execution of clinical trials, working closely with the clinical research site management and the Principal Investigator (PI). While the PI oversees the overall trial conduct, the CRC is responsible for managing and coordinating daily activities related to the clinical study.

Key Responsibilities:

  • Assist the trial Investigator in evaluating and screening potential participants for study eligibility.
  • Maintain accurate case report forms, charts, and documentation.
  • Provide mentorship and training to junior clinical research coordinators and research assistants.
  • Ensure compliance with established research protocols and applicable regulations throughout all clinical activities.
  • Collect and input data as required.
  • Support management in the selection and onboarding of new hires.
  • Assist with the initiation, management, and closure of studies as needed.
  • Demonstrate flexibility in handling various study assignments.

Qualifications:

  • 1-2 years of experience as a Clinical Research Coordinator.
  • Current certification/license in phlebotomy in the state of California.
  • Strong verbal and written communication skills.
  • Ability to quickly learn and comprehend complex protocols and follow detailed instructions.
  • Commitment to maintaining confidentiality in accordance with HIPAA guidelines.
  • Extensive knowledge of clinical trials through education or experience.
  • Preferred: Successful completion of GCP Certification and Advanced CRC training.
  • Detail-oriented with strong interpersonal skills.
  • Familiarity with federal regulations related to human subject protection.

About M3:
M3 USA is dedicated to advancing healthcare through innovative digital solutions across various sectors, including life sciences and pharmaceuticals. Our mission is to leverage technology for improved health outcomes and more efficient healthcare systems.

We pride ourselves on fostering a dynamic work environment where each team member contributes to significant advancements in global health. Joining M3 USA provides an opportunity to be at the forefront of healthcare innovation and to make a meaningful impact in the industry.

Benefits:
We offer competitive compensation and a comprehensive benefits package, including:

  • 401(k) with matching contributions
  • Dental and health insurance
  • Disability and life insurance
  • Flexible spending accounts
  • Paid time off
  • Vision insurance

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