Associate Auditor, Quality Assurance - San Antonio - On-site

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 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 

• Always representing Worldwide in a professional manner (verbal, written, and in appearance) when interacting with sponsors, volunteers, outside vendors, and fellow employees.

• Assists the QA team with other auditors to plan, conduct and complete written reports for each audit assigned.

• Monitors the projects and audit status in assigned areas and provides QA Management with status upon request.

• Builds and maintains good working relationships with internal clients and QA team.

• Oversees the maintenance of records for each audit.

What you will bring to the role 

• Develops and maintains knowledge of applicable GxP requirements

• Develops and maintains knowledge of Worldwide’s policies and procedures

• Ability to interact professionally and to work independently or in teams

• Excellent oral and written skills

• Ability to prioritize work and define steps needed to achieve assigned project goals

• Ability to speak, read and write English fluently

• Experience with Microsoft Word applications and the ability to learn internal computer systems as necessary.

Your experience 

• Required: Bachelor’s degree preferably in life science or equivalent experience gained by working in a relevant area (clinical setting, laboratory, etc.).

• Preferred: 0-2 years’ experience in quality assurance, regulatory affairs, auditing, clinical research, monitoring, laboratory, or other relevant area.

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, et