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Clinical Trials QA Manager - Remote

  • Location: New Iberia, 02895
  • Salary: 90.0
  • Job Type:Contract

Posted 20 days ago

Interested in getting into the high-in-demand healthcare field? Check out this opportunity!
 
Position: Clinical Trials QA Manager
Location: Remote
Hourly Rate: $ 90.00/hr.
Term: 3 Months Contract

Day-to-Day Responsibilities: 
  • Manage Customer qualification activities, including audit questionnaires, document reviews, etc.
  • Coordinate with subject matter experts (SME) from across the business to ensure timely completion of qualification activities
  • Coordinate internal Quality and Legal review
  • Maintain dashboards and provide weekly updates to Quality Leads
  • Manage communications with Customers
  • Be proactive and exercise initiative in identifying, tracking, and mitigating and/or escalating potential risks; establish contingency plans and initiate corrective action, as needed
  • Manage process improvements to enhance Quality processes, focusing initially on identifying and implementing improvements to the Customer Qualification process based on the CTS strategy and vision
  • Maintain organizational standards of satisfaction, quality, and performance
  • Support Quality Assurance team, as needed (e.g., document management, vendor management)

Is it a good fit? (Requirements):
  • Bachelor's degree in applied sciences, healthcare, business, or related field
  • At least 3 years of experience in managing/coordinating initiatives in the Clinical Research environment
  • Working knowledge of FDA GCP & ICH regulatory requirements
  • Excellent organizational and people skills
  • Clear, effective communication skills, both written and verbal
  • Above average organizational skills
  • Ability to learn quickly and adapt to a changing environment; proactive in seeking out information when necessary
  • Team player; works well with others
  • Strong working knowledge of Microsoft Office
  • Comfortable working in fast-paced environment
  • Ability to balance multiple tasks and shift priorities rapidly, in a responsive and effective manner
  • Working knowledge of FDA GCP & ICH regulatory requirements

Even better if you have:
  • At least 5 years of experience in managing/coordinating initiatives in the Clinical Research environment
  • Experience managing internal audits and Customer qualification audits
  • Experience conducting audits of GCP Vendors
  • Experience managing GCP Vendors (e.g., vendor oversight requirements, Quality Agreements)

Candidates will be responsible for following the client's COVID-19 protocols. Please refer to your MATRIX representative for specifics.

About Us

At MATRIX, we expertly match talented professionals with job opportunities to elevate careers. Since 1983, we have placed thousands of professionals at innovative clients across every industry ranging from small startups to Fortune 50 companies. It’s why we’re consistently in the top 25 of all U.S. IT staffing firms and why our consultants rate us well above the industry average, earning us ClearlyRated's Best of Staffing awards year after year. People come to us for a job, and stay with us because of our top-notch consultant care.

MATRIX is and Equal Employment Opportunity employer and provides reasonable accommodations for qualified individuals.  Supporting medical or religious documentation will be required where applicable. If you are a qualified individual with a disability, you may request a reasonable accommodation under the American Disability Act (ADA) by emailing MATRIX_HR@MatrixRes.com. To ensure a quick response to your request, please use the words “Accommodation request” as the subject line of your email.