Clinical Trial Manager - US - Remote
What you will do
• Provide leadership and direction to clinical site management team members from study start through to closure
• Serve as Site Management primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to:
1. Primary Sponsor contact
2. Investigator and Bid Defense Meetings
3. Internal and External study team calls
4. Project-specific Audits / Inspections
• Manage monitoring deliverables to achieve study budget and identify Out of Scope Activities
• Oversee compliance to the Clinical Monitoring Plan, including site visits, outstanding trip reports and visit follow up letters
What you will bring to the role
• Excellent interpersonal, oral, and written communication skills in English and in local language
• 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 within a sponsor contact
• Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
• Four-year college curriculum or equivalent with a major concentration in biological, physical or health studies and a minimum experience of 3 years as a Senior Clinical Research Associate (or equivalent), OR
• Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree preferred) and a minimum experience of 5 years as a Senior Clinical Research Associate, OR
• Minimum 6-month experience functioning as CTM/LCRA (or equivalent); supporting main CTM and coordinating clinical operations activities
• Willingness to travel
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.
• Provide leadership and direction to clinical site management team members from study start through to closure
• Serve as Site Management primary point of contact and representative for clinical monitoring and site activities within the project, including, but not limited to:
1. Primary Sponsor contact
2. Investigator and Bid Defense Meetings
3. Internal and External study team calls
4. Project-specific Audits / Inspections
• Manage monitoring deliverables to achieve study budget and identify Out of Scope Activities
• Oversee compliance to the Clinical Monitoring Plan, including site visits, outstanding trip reports and visit follow up letters
What you will bring to the role
• Excellent interpersonal, oral, and written communication skills in English and in local language
• 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 within a sponsor contact
• Proficiency in Microsoft Office, CTMS, and EDC Systems
Your experience
• Four-year college curriculum or equivalent with a major concentration in biological, physical or health studies and a minimum experience of 3 years as a Senior Clinical Research Associate (or equivalent), OR
• Two-year college curriculum or equivalent education/training (nursing degree or equivalent life science degree preferred) and a minimum experience of 5 years as a Senior Clinical Research Associate, OR
• Minimum 6-month experience functioning as CTM/LCRA (or equivalent); supporting main CTM and coordinating clinical operations activities
• Willingness to travel
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.