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
• CNS/Neurology experience is required
• Experience in Multiple Sclerosis and/or Alzheimer's Disease a plus
• 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 Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.