Project Manager (Cardiac Safety)

Location: Remote within the United States

Company

Clinical trial technology and services focused on improving evidence for drug development programs.

What you will do

• Lead the planning, setup, monitoring, and closeout phases of cardiac safety clinical studies.
• Translate customer requirements into actionable plans and maintain study documentation, reports, and data archiving.
• Coordinate equipment distribution and tracking throughout study execution.
• Monitor timelines and manage budgets, revenue forecasting, scope changes, and invoice reconciliation.
• Identify and mitigate study risks, resolve client issues, and manage internal and external stakeholder communications.
• Represent study services in client meetings and support onboarding and training for new project management team members.

Requirements

• Bachelor’s degree or equivalent practical experience in project management or a related field.
• 1–4 years of project management experience in the pharmaceutical, clinical, or related industry.
• Knowledge of the drug development lifecycle and clinical trial processes.
• Strong organizational, time management, prioritization, communication, and interpersonal skills.
• Effective communication in English and proficiency in Microsoft Office applications.
• Valid passport and willingness to travel up to approximately 20%.

Culture & Benefits

• Cross-functional collaboration with internal teams, clients, investigators, and study sites.
• Opportunity to contribute to clinical trial delivery and drug development programs.
• Fast-paced environment requiring responsiveness, accountability, and management of multiple priorities.
• Remote work arrangement within the United States with travel as needed.