PRN Research Associate 1 - San Antonio, TX - In Office

Worldwide Clinical Trials - USA

San Antonio, TX

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 PRN Research Associate does at Worldwide
The PRN Research Associate 1, has familiarity with processing and reviewing clinical documentation, interacting with participants, and accommodating competing priorities in a dynamic clinical research environment.
What you will do
Conduct screening visits for participant recruitment into clinical trials under the supervision of the Screening Supervisor.
Review study protocol and informed consent form for studies.
Ensure electronic and paper source documents for the trial are accurate according to study specific protocol
Prepare and maintain study-specific screening documents and study folders.
Responsible for entering and updating participants in vendor study eligibility portal
Responsible for reviewing the informed consent form, medical history, inclusion/exclusion criteria, and other study documents as required with participants to determine eligibility.
What you will bring to the role
Excellent written and oral communication skills.
Ability to understand complex written and oral instructions.
Excellent attention to detail resulting in high-quality work.
Exceptional organizational skills.
Ability to set and meet deadlines.
Your experience
Preferred:
Bachelor’s Degree (preferably in the field of Life Sciences or Health).
Six months or more experience in health care.
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 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’reon a mission to hire thevery bestand 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 .

Posted 2025-11-06

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