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, a global team of over 3,500 experts, bright thinkers, dreamers, and doers, 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 seek others who share this pursuit.
Why Worldwide
We believe everyone plays an important role in making a difference for patients and caregivers. From accessible leaders to supportive teams, we are committed to enabling professionals from all backgrounds to succeed. We prioritize diversity and inclusion to foster 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 Site Management does at Worldwide
Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) are vital in ensuring our clinical research programs are executed with quality and excellence, providing the care and passion patients deserve. These roles are the backbone of every strong CRO, driving scientific breakthroughs and leading clinical trials. We offer an uncommon experience with a team unlike any other.
At Worldwide, we balance fun with the serious business of changing lives. Our culture is values-driven, empowering our team to treat every trial as if a patient’s life depends on it — because it does. Our leaders work alongside you, committed to advancing science and supporting our customers.
What you will do
1. Provide leadership and direction to the clinical site management team from study start to closure.
2. Serve as the primary contact and representative for site management within the project, including monitoring and site activities.
3. Act as the primary sponsor contact.
4. Manage monitoring deliverables to meet the study budget and identify out-of-scope activities.
What you will bring to the role
* Excellent interpersonal, oral, and written communication skills in English.
* Ability to lead and motivate a remote team.
* Initiative and problem-solving skills with solution-oriented thinking.
* Strong customer focus and professional interaction with sponsors.
* Proficiency in Microsoft Office, CTMS, and EDC systems.
Your experience
* Bachelor’s Degree or Nursing Degree required.
* At least 2 years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or similar role.
* At least 3 years’ experience as a Clinical Research Associate.
* Oncology (solid tumor) experience is required.
* Willingness to travel up to 30%.
We are passionate about the impact of our work on bettering lives. To explore other roles, visit our careers page at Discover a world of difference at Worldwide. For more information, visit www.Worldwide.com or connect with us on LinkedIn.
Worldwide is an equal opportunity employer committed to diversity and inclusion, fostering an environment where everyone can succeed and be respected. We provide equal employment opportunities regardless of race, ethnicity, gender, age, disability, or other protected classes.
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