Global Clinical Trials Lead Medical Devices

Bausch Health; United States; On-site; USD 158,000 - 218,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401(k)

Job summary

Solta Medical seeks a Senior Clinical Project Manager to lead end-to-end planning and execution of complex global clinical trials for medical devices. You will manage site relationships, enrollment tracking, and regulatory compliance, ensuring timelines and budgets are met across multiple studies.

The role requires strong cross-functional collaboration with Medical Affairs, Regulatory, Data Management, and Quality, with extensive CRO/vendor oversight and inspection readiness.

Qualifications

• Bachelor's degree required; life sciences or nursing preferred.
• 8+ years of clinical research execution in medical devices.
• Experience leading end-to-end clinical trial execution (feasibility, start-up, enrollment, monitoring, close-out).
• Understanding regulatory requirements for clinical study reports.

Responsibilities

• Own end-to-end planning and execution of a portfolio of complex clinical research projects globally.
• Manage day-to-day study operations, site relationships, enrollment tracking, and regulatory compliance.
• Maintain study timelines and metrics; lead study-specific meetings.
• Oversee CRF design, TMF management, and vendor oversight.
• Collaborate cross-functionally to ensure study success and regulatory alignment.
• Oversee CROs and external vendors, including budgeting and performance reviews.

Skills

Project management

Cross-functional collaboration

Regulatory compliance

Clinical trial execution

Vendor management

Budget management

Communication

Education

Bachelor's degree in life sciences or nursing

Tools

MS Office

EDC systems

CTMS

Job description

Solta Medical seeks a Senior Clinical Project Manager to lead end-to-end planning and execution of complex global clinical trials for medical devices. You will manage site relationships, enrollment tracking, and regulatory compliance, ensuring timelines and budgets are met across multiple studies.

The role requires strong cross-functional collaboration with Medical Affairs, Regulatory, Data Management, and Quality, with extensive CRO/vendor oversight and inspection readiness.