Senior Auditor, Audits and Inspections Program - US/Canada - Remote

Worldwide Clinical Trials; North Carolina; Remote; USD 75,000 - 105,000; Full time

Job summary

A leading clinical research organization is seeking a Senior Auditor for their Audits and Inspections Program, offering the opportunity to work remotely in North America. The ideal candidate will have extensive GCP auditing experience and be responsible for ensuring compliance with regulatory standards while driving quality improvements in processes. This role involves hosting audits, overseeing QA deliverables, and being a subject matter expert in QA processes, contributing to the overall mission of improving patient care globally.

Qualifications

• Minimum 5 years of GCP, GcLP, GLP, GVP experience.
• Excellent knowledge of FDA regulations.
• Experience in trending and analysis methodologies.

Responsibilities

• Hosts external audits and regulatory inspections.
• Ensures quality deliverables in compliance with regulations.
• Develops and executes QA goals and objectives.

Skills

Quality Management

Regulatory Compliance

Conducting Audits

Process Improvements

Education

M.S. in a scientific or allied health field

Tools

Microsoft Office Suite

Trackwise

SharePoint

Job description

Senior Auditor, Audits and Inspections Program - US/Canada - Remote

Join to apply for the Senior Auditor, Audits and Inspections Program - US/Canada - Remote role at Worldwide Clinical Trials

Senior Auditor, Audits and Inspections Program - US/Canada - Remote

Join to apply for the Senior Auditor, Audits and Inspections Program - US/Canada - Remote role at Worldwide Clinical Trials

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Who We Are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

Who We Are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!

What The Quality Assurance Department Does At Worldwide

The Quality Assurance department sets the bar high when it comes to quality. We are committed to exceeding the quality standards required by our sponsors, study participants, and regulatory authorities. Our QA culture is based on an environment where staff are trained, energized, and empowered to deliver high-quality products to our employees and customers.

What You Will Do

• Champions and adheres to Worldwide’s Quality Management System (QMS).
• Serves as a positive ambassador of the QA organization with internal and external customers.
• Develops and executes to personal and QA goals and objectives.
• Hosts external audits and regulatory inspections.
• Ensures quality deliverables, on time, and in compliance with regulations and Worldwide processes.
• Oversees, monitors and reports on QA audits to ensure timely completion of applicable CAPAs to prevent reoccurrence and to drive process improvements.
• Oversees the maintenance and archiving of records for each audit.
• Participates in the driving continuous process improvements.
• Participates in the development and review of AIP Quality Management Documents, as assigned.
• Assists in developing training material and/or delivers training related to audits and inspections.
• Serves as a Subject Matter Expert on QA Quality Management processes for audits.
• Communicates relevant regulatory intelligence that has impact on the QMS to the QA team.
  
  

What You Will Bring To The Role

• Possesses broad expertise related to understanding the principles and application of quality and regulatory compliance related to GxP activities.
• Excellent working knowledge of ICH Guidelines, FDA regulations, European Directives, MHRA Statutory Instruments, and AIFA CRO Decree.
• Possesses broad experience related to understanding the principles and application of quality and regulatory compliance related to GxP activities, specifically GCP.
• Excellent experience in conducting QA Audits, specifically GCP for each type (i.e. Clinical Investigator Audits, Vendor Audits, Internal Process Audits, For-cause Audits, Document Audits, etc.).
• Previous experience in trending and analysis methodologies.
  
  

Your Experience

• M.S. in a scientific or allied health filed and 5+ years of relevant GCP, GcLP, GLP, GVP, and / or GPP experience.
• Excellent understanding of the Drug Development Process.
• Minimum 3 years of Quality Assurance auditing experience.
• IT literate, experienced with Microsoft based applications, including proficiency in Excel, Word, Trackwise, SharePoint, and PowerPoint.
• Occasional domestic traveling required.
  
  

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Accounting/Auditing and Finance

• Industries

  Research Services

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