Clinical Quality Specialist

3 days ago


California, United States GForce Life Sciences Full time
Clinical Quality Specialist Opportunity

GForce Life Sciences is seeking a highly skilled Clinical Quality Specialist to join our team. As a Clinical Quality Specialist, you will play a critical role in ensuring the quality and compliance of our clinical research activities.

Key Responsibilities:

  • Support general audit administration, including tracking and following up on audit deliverables.
  • Support inspection readiness activities through quality checks and document reviews.
  • Provide clinical study compliance-related support, including sponsor oversight and compliance-related questions.
  • Support procedure improvement opportunities and GCP training needs.
  • Support quality system implementation in clinical research settings, including Corrective and Preventive Action activities (CAPA).

Requirements:

  • Bachelor's degree in a scientific or engineering-related field.
  • Experience supporting clinical quality activities and ensuring GCP compliance in GCP and FDA-regulated activities.
  • Medical devices research experience is preferred but not mandatory.
  • Exposure to clinical research audits and/or quality system familiarity is an asset.

What We Offer:

  • Contract through the end of the year, with a strong possibility of extension.
  • Hybrid locations: Maple Grove, MN; Los Angeles, CA; Dallas, TX.
  • Benefits included (Medical, Dental, Vision, 401k).
  • Full-time (40 hours/week).

About GForce Life Sciences:

GForce Life Sciences is a global medical device company dedicated to providing innovative solutions for the healthcare industry. We are committed to excellence and quality in all our endeavors.



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