Worldwide Clinical Trials·Durham, North Carolina
Manage research activities at clinical sites, including site identification, start-up activities, and regulatory document collection. Conduct study initiation visits and ensure compliance with informed consent and safety reporting throughout the study lifecycle.
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.
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 Clinical Operations does at Worldwide
At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.
Are you a motivated Clinical Research Associate with 2–3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development, provide meaningful career progression, and give you the opportunity to work alongside experienced clinical research professionals?
If so, we'd love to hear from you.
We are looking for a CRA II who is eager to expand their monitoring expertise, build strong site relationships, and grow into a senior clinical operations role. This position is ideal for someone who has established a solid foundation in site monitoring and is ready to accelerate their career within a supportive, collaborative, and quality-focused organization.
What you will do
Your experience
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $79,500.00 - $158,500.00
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 [https://worldwide.wd1.myworkdayjobs.com/External]! For more information on Worldwide, visit www.Worldwide.com [http://www.Worldwide.com] or connect with us on LinkedIn [https://www.linkedin.com/company/worldwide-clinical-trials-inc-/].
Requires 2-5 years of experience as a traveling Clinical Research Associate with specific experience in Psychiatric monitoring. A 4-year university degree or Nursing degree is required, along with a willingness to travel regionally.
Market context
Clinical Research Associate II roles in psychiatry are typically competitive because employers want candidates with prior traveling CRA experience, psychiatric monitoring exposure, and the flexibility to travel regionally from North Carolina. This role stands out for applicants who can show strong site oversight, protocol compliance, and comfort working remotely across multiple studies. Review the AI-summarized requirements and benefits here to save time, then confirm your travel availability and prepare examples of psychiatric monitoring work before applying.
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