Clinical Project Manager

Responsibilities

• Lead all clinical study operations including strategic/tactical planning, timelines, budgets, and site management
• Facilitate communication between sponsors, study teams, and functional groups
• Manage and mentor study team members to ensure professional development
• Provide financial oversight of study budgets and track out-of-scope activities
• Drive development and maintenance of project plans including monitoring and eTMF plans
• Manage studies in compliance with GCP, SOPs, and regulatory requirements
• Assess and manage study risks and escalate issues appropriately
• Oversee activities and deliverables of outside vendors

Requirements

• RN or Bachelor/advanced degree in biological sciences or related field
• Equivalent combination of relevant experience, education, or training and previous CRA experience
• Proven effectiveness as a team leader
• Experience managing multifaceted studies from inception to completion
• Experience managing projects in a virtual environment
• Proficiency in Microsoft Word, Excel, and PowerPoint

Preferred Qualifications

• Experience with MS Project and OneNote

Benefits

• Full medical, dental, and vision insurance options
• Flexible PTO
• 401(k) plan with company match
• Professional growth and development support

About the Company

ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996, supporting pharmaceutical, biotech, and medical device industries.