Senior Clinical Trial Manager - Oncology - U.S. - Remote
Job Description
What Clinical Operations Site Management does at Worldwide
Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.
These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role in every clinical trial. All CROs will promise you growth, opportunity, and maybe even a challenge. But we offer more than that. We offer an uncommon experience – one you can’t get anywhere else, with a team unlike anyone else.
At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you, committed to advancing science and moving mountains for our customers.
What you will do
• 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
What you will bring to the role
• 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
Your experience
• Bachelor’s Degree or a Nursing Degree required
• 1+ 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%
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 ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Apply tot his job
Apply To this Job
What Clinical Operations Site Management does at Worldwide
Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.
These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role in every clinical trial. All CROs will promise you growth, opportunity, and maybe even a challenge. But we offer more than that. We offer an uncommon experience – one you can’t get anywhere else, with a team unlike anyone else.
At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up. We empower our team members to treat every trial like a patient’s life depends on it – because it does. Our leaders are in the trenches with you, committed to advancing science and moving mountains for our customers.
What you will do
• 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
What you will bring to the role
• 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
Your experience
• Bachelor’s Degree or a Nursing Degree required
• 1+ 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%
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 ! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Apply tot his job
Apply To this Job