Remote Clinical Project Manager - Medical Device Trials

Surf Search Inc.; United States; Remote; USD 110,000 - 150,000; Full time

Job summary

Surf Search Inc. is seeking a Clinical Project Manager to oversee planning, execution, and completion of clinical studies supporting medical device products.

You will coordinate with internal teams, sites, CROs, and vendors to ensure studies stay on schedule, within budget, and in compliance with protocols and regulations. The ideal candidate has hands-on experience managing device studies, CROs, budgets, and timelines, plus strong communication and multitasking abilities.

Qualifications

• Bachelor's degree required in life sciences, nursing, engineering, or related field.
• 6+ years of clinical research or trial management experience.
• Experience with medical device studies and regulatory submissions.

Responsibilities

• Manage clinical studies from planning and feasibility through close‑out
• Develop and maintain study timelines, budgets, project plans, and deliverables
• Manage CROs, core laboratories, imaging vendors, consultants, and other third parties
• Coordinate cross‑functional clinical teams and external study partners
• Monitor study progress, data quality, risks, budgets, and timelines
• Support clinical and regulatory documentation, submissions, and reporting
• Ensure studies comply with protocols, GCP/ICH guidelines, applicable regulations, and internal procedures
• Communicate study status, risks, and milestones to leadership and project teams

Skills

Project management

Communication skills

Vendor management

GCP/ICH knowledge

CTMS/EDC proficiency

Budgeting

Education

Bachelor's degree in life sciences, nursing, engineering, or related field

Tools

CTMS

EDC systems

Microsoft Office

Job description

Surf Search Inc. is seeking a Clinical Project Manager to oversee planning, execution, and completion of clinical studies supporting medical device products.

You will coordinate with internal teams, sites, CROs, and vendors to ensure studies stay on schedule, within budget, and in compliance with protocols and regulations. The ideal candidate has hands-on experience managing device studies, CROs, budgets, and timelines, plus strong communication and multitasking abilities.