Clinical Project Manager - Remote

Overview

The Clinical Project Manager (CPM) will lead cross-functional study teams to plan and execute successful clinical studies, from concept through study completion.

In Short

• Overall management of multiple clinical studies in compliance with internal and external standards.
• Develop study protocols/amendments and acquire IRB approval.
• Prepare and/or review study-related plans and crucial documents.
• Develop and track the clinical study budget.
• Supervise and review results produced by study team members.
• Interact with investigators and site staff on study-related issues.
• Coordinate and lead external clinical suppliers supporting studies.
• Train new team members and clinical site personnel.
• Conduct on-site visits and monitoring activities as needed.
• Develop Clinical Investigation Reports upon study completion.

Requirements

• BA/BS in a health science field with >5 years relevant experience OR MA/MS in a health science field with >2 years relevant experience.
• Three or more years of experience handling clinical research studies.
• Solid understanding of Good Clinical Practice (GCP), FDA and ISO regulations.
• Ability to work independently and lead multiple projects.
• Excellent social skills and ability to interact with physicians and scientists.
• Strong communication skills (oral and written).
• Computer proficiency including Microsoft Office Suite.
• Ability to travel approximately 10%-20%.

Benefits

• Supportive team environment that encourages growth.
• Opportunity to work on impactful health solutions.
• Flexible work-life balance.
• Commitment to diversity and inclusion.
• Equal Opportunity Employer.