Senior Clinical Trial Manager - Oncology - U.S. (Remote)
About The Position
Worldwide Clinical Trials is a global, midsize CRO that is dedicated to pushing boundaries and innovating to find cures for the world's most persistent diseases. We are a global team of over 3,500+ experts committed to changing the way the world experiences CROs. Our mission is to work with passion and purpose every day to improve lives. We believe everyone plays an important role in making a world of difference for patients and their caregivers. We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity, and we are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Clinical Operations Site Management at Worldwide involves Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) who play a vital role in ensuring clinical research programs are executed with quality and excellence. These roles are the backbone of every strong CRO, driving scientific research and leading clinical trials. We offer an uncommon experience with a team unlike any other, balancing fun with the serious business of changing lives. Our values-driven culture empowers team members to treat every trial with utmost importance, and our leaders are committed to advancing science and supporting our customers.
Requirements
- Excellent interpersonal, oral, and written communication skills in English
- Ability to lead and motivate a team remotely
- Demonstrate initiative and problem-solving skills by offering solutions when obstacles are identified
- Strong customer focus, ability to interact professionally with a sponsor contact
- Proficiency in Microsoft Office, CTMS, and EDC Systems
- Bachelor’s Degree or a Nursing Degree required
- 2+ years’ experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role
- 3+ years’ experience as a Clinical Research Associate
- Oncology experience is required
- Willingness to travel up to 30%
Responsibilities
- Provide leadership and direction to clinical site management team members from study start through to closure
- Serve as Site Management’s primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to Primary Sponsor Contact
- Manage monitoring deliverables to achieve the study budget and identify out-of-scope activities
Benefits
- Competitive benefits package
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Senior
