Clinical Research Coordinator: Trials Operations & Compliance

Prolerity Clinical Research, Inc.

Metairie (LA)

On-site

USD 48,000 - 64,000

Full time

9 days ago

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Job summary

Prolerity Clinical Research, Inc. in Metairie, LA seeks a Clinical Research Coordinator to oversee daily operations of assigned studies, ensuring compliance with protocols, regulations, and ethics.

You will own study coordination, data management, sponsor communication, and support start-up through close-out, collaborating with investigators, staff, sponsors, and CROs. The ideal candidate has a bachelor’s degree and at least two years in clinical research or trial management, with strong

Qualifications

  • Bachelor’s degree required.
  • Minimum of two years of clinical research or clinical trial management experience.
  • Phlebotomy experience preferred.
  • Prior experience with regulatory submissions is a plus.

Responsibilities

  • Organize and coordinate all aspects of trials from initiation through close-out.
  • Support start-up activities including regulatory submissions and site activation.
  • Attend investigator meetings and site initiation visits.
  • Manage visit schedules and coordinate study-related activities across clinical teams.
  • Monitor subjects and report adverse events in collaboration with the PI and staff.
  • Maintain source documentation, CRFs, regulatory files, and study records.

Skills

Leadership
Organization
Regulatory compliance
Communication
Multitasking
Time management

Education

Bachelor’s degree

Tools

EDC systems
Medical records software
Office software

Job description

Prolerity Clinical Research, Inc. in Metairie, LA seeks a Clinical Research Coordinator to oversee daily operations of assigned studies, ensuring compliance with protocols, regulations, and ethics.

You will own study coordination, data management, sponsor communication, and support start-up through close-out, collaborating with investigators, staff, sponsors, and CROs. The ideal candidate has a bachelor’s degree and at least two years in clinical research or trial management, with strong

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