Remote Clinical Project Manager
at MCRA

Summary

Join our client's team as a Contract Clinical Project Manager for a part-time, 10-20 hours per week, 6-month assignment. The successful candidate will manage assigned investigator sites and oversee site staff, ensuring project deliverables are met within scope, timeline, and budget.

Requirements

• Bachelor's degree (B.A./B.S.) in life sciences, healthcare, or a related scientific discipline, or be a Registered Nurse/Allied Health Professional with clinical research experience
• Clinical Research certification preferred but not required
• 2+ years of direct, on-site clinical trial monitoring experience required
• Medical device experience required; vascular experience is highly desirable
• Strong knowledge of ICH guidelines for GCP
• Experience using Electronic Data Capture (EDC) and clinical trial management systems (Smart Trial preferred but not required)
• Strong written and verbal communication and presentation skills
• Strong research, analytical, critical-thinking, and problem-solving skills
• Proficiency with MS Office Suite (Outlook, Word, PowerPoint, Excel) and internet applications

Responsibilities

• Coordinate and manage all phases of clinical trials from start-up to close-out
• Ensure project deliverables are met within scope, timeline, and budget
• Develop and maintain positive relationships both internally and externally, including clients, team members, and site personnel (PIs, Study coordinators, etc.)
• Maintain clear and consistent communication with surgeons, site staff, and internal teams
• Manage retrospective patient data collection projects
• Exhibit great customer service skills and work effectively with minimal oversight/training
• Maintain current knowledge of GCP and FDA guidance as it relates to clinical research
• Work independently and proactively

Benefits

Occasional travel may be required for site visits and/or meetings