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Premier Research

Global Quality Coordinator

Posted Yesterday
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Remote
Hiring Remotely in United States of America
Senior level
Remote
Hiring Remotely in United States of America
Senior level
The Global Quality Coordinator assists in audits, manages compliance issues, maintains the quality management system, and drives process improvement initiatives.
The summary above was generated by AI
Premier Research is looking for a Global Quality Coordinator to join our Functional Services Provider (FSP) team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

  • We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

  • Your ideas influence the way we work, and your voice matters here.

  • As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What you'll be doing:

  • Assists and participates in contracted audits (investigator sites, trial master files, databased, study reports etc.) and internal audits (systems, processes, vendors, computer system validation etc.) across global operations, (including preparation of audit plans, audit checklists, audit reports and certificates

  • Helps project manage compliance issues, running investigations with operational teams

  • Assists the maintenance of the Global Quality Management System

  • Supports Premier Research in ensuring the effectiveness of the Quality Management System and the quality of the deliverables

  • Assist in the conduct detailed QA review of SOPs prior to approval

  • Drives input into process improvement initiatives across the company

What we are searching for:

  • Bachelor’s degree, or international equivalent from an accredited institution, in Health or Life Sciences, or equivalent experience

  • At least 5 years specialized GCP and ISO experience in auditing clinical trials including auditing internal processes and performing vendor audits

  • Ability to interpret research protocols and audit medical records

  • Experience in hosting and responding to regulatory inspections preferred

  • Experience with paper-based data management systems; experience with RDC/EDC data

  • Preferred Location: East Coast

  • Please note this is a 12 month 1099 contractor opportunity

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role.

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status

Top Skills

Edc
GCP
Iso
Paper-Based Data Management Systems
Rdc

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