Worldwide Clinical Trials·Boise, Idaho
Manage research activities at clinical sites, including site identification, start-up, and close-out activities. Conduct study initiation visits and ensure compliance with regulatory requirements and safety reporting.
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.
As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.
Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.
We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!
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 - $97,000.00 - $193,000.00
The salary range provided is intended to give candidates an understanding of potential earnings.
Compensation will fall within the provided range, and it not a guarantee of exact salary.
The final salary will be determined based on relevant experience, performance, education, and internal equity.
In addition to base salary, we offer a competitive benefits package depending on location.
We ensure pay equity and transparency and comply with all applicable labor laws.
Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
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 a university or nursing degree and at least 5 years of experience as a CRA, specifically within Oncology and Rare Disease. Must be fluent in English and willing to travel regionally.
Market context
Senior Clinical Research Associate roles in oncology are typically in demand where sponsors are running complex trials and need experienced monitors who can manage site quality, compliance, and patient safety. This category is competitive because employers often look for deep oncology and rare disease experience, strong English communication, and willingness to travel regionally. Review the AI-summarized requirements and benefits on this platform to quickly compare fit, then tailor your application to highlight monitoring experience, therapeutic-area exposure, and travel readiness.
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