Sr. Clinical Project Manager / Clinical Project Manager

Hart Clinical Consultants; United States; On-site; USD 129,000 - 175,000; Full time

Job summary

Hart Clinical Consultants is seeking an experienced Clinical Project Manager to lead clinical trials, ensuring compliance with regulatory standards and overseeing operational and financial aspects. The role requires significant experience in project management within the CRO or medical device industry and offers a competitive salary range based on location and expertise.

Qualifications

• Experience in managing medical device clinical trials in a CRO environment is required.
• Proven experience in clinical project management, Clinical Operations, or Data Management.

Responsibilities

• Lead and manage all phases of clinical trials to ensure quality, compliance, timelines, and budgets are met.
• Serve as the primary point of contact for internal stakeholders and clients.

Skills

Clinical Project Management

Compliance

Stakeholder Communication

Problem-Solving

Education

4+ years in CRO, pharmaceutical, biotech, or medical device industry

Job description

Sr. Clinical Project Manager / Clinical Project Manager

Sr. Clinical Project Manager / Clinical Project Manager

Sr. Clinical Project Manager / Clinical Project Manager

Hart Clinical Consultants (HCC) is seeking an experienced and driven Clinical Project Manager (CPM) to lead the planning, execution, and completion of clinical trials in accordance with regulatory standards and company procedures. As the CPM, you will oversee both the operational and financial aspects of assigned studies, guiding cross-functional teams from study start-up through closeout.

Key Responsibilities:

• Lead and manage all phases of clinical trials to ensure quality, compliance, timelines, and budgets are met
• Direct project teams in the successful execution of clinical protocols and delivery of contracted HCC services
• Serve as the primary point of contact for internal stakeholders and clients, providing clear communication and proactive problem-solving
• Oversee study start-up, site management, monitoring activities, and closeout procedures
• Ensure adherence to regulatory requirements, GCP, SOPs, and project-specific guidelines

Preferred Candidate Location:

• Based in U.S. Eastern or Central Time Zones (strongly preferred)

Requirements:

• Minimum of 4 years of experience in the CRO, pharmaceutical, biotech, or medical device industry
• Proven experience in clinical project management or related roles such as Clinical Operations, Clinical Monitoring, or Data Management
• Hands-on experience managing medical device clinical trials in a CRO environment is required

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management and Information Technology

• Industries

  Research Services

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