Job Description
- 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.
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