Remote Clinical Trial Project Manager

Heart Rhythm Clinical Research Solutions; United States; Remote; USD 110,000 - 150,000; Full time

Job summary

Heart Rhythm Clinical Research Solutions is seeking a Project Manager to lead planning, coordination, and execution of clinical trials remotely across the United States. The role requires ensuring trials comply with protocols, SOPs, GCP, and regulatory standards while coordinating budgets, timelines, and resources.

You will be the primary liaison for sponsors, investigators, and stakeholders, managing risks and ensuring data accuracy.

Qualifications

• Bachelor’s degree in life science or related field; master’s or certification preferred.
• 5+ years in clinical project management at CRO/biotech/pharma.
• Strong PM skills with multitasking ability.
• Excellent communication and interpersonal skills.
• Proficiency in project management software/tools.

Responsibilities

• Plan, coordinate, and oversee all stages of clinical trials from planning to closeout.
• Ensure trials follow protocol, SOPs, GCP, and regulatory requirements.
• Serve as primary contact for sponsors, investigators, and stakeholders with updates.
• Identify risks and implement mitigation strategies.
• Collaborate with internal teams and external vendors to meet goals.
• Oversee data management ensuring data accuracy and integrity.
• Lead project meetings and document key actions and decisions.
• Prepare and present reports to senior management.
• Complete mandatory training on time.

Skills

Project management

Communication

Regulatory knowledge

GCP

Data management

Budgeting

Risk management

Vendor coordination

Education

Bachelor’s degree in life science

Master’s degree or certification preferred

Tools

Project management software

Job description

Heart Rhythm Clinical Research Solutions is seeking a Project Manager to lead planning, coordination, and execution of clinical trials remotely across the United States. The role requires ensuring trials comply with protocols, SOPs, GCP, and regulatory standards while coordinating budgets, timelines, and resources.

You will be the primary liaison for sponsors, investigators, and stakeholders, managing risks and ensuring data accuracy.