Senior Clinical Project Manager – Cardio-Metabolic (Remote)

Regulatory Jobs; United States; Remote; USD 120,000 - 160,000; Full time

Benefits offered by this job

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability

Learning and development opportunities

Job summary

ICON is seeking a Senior Clinical Project Manager to join our Internal Medicine team. This remote role in the United States focuses on leading and delivering complex clinical projects across global sites.

You will develop plans, mentor teams, collaborate with stakeholders, and drive documentation and reporting to stakeholders. A strong background in pharma/biotech and excellent communication are essential.

Qualifications

• Bachelor’s degree or master’s in Project Management, Business Administration, or related field.
• Extensive experience in global clinical project management in pharma/biotech.
• Strong proficiency in PM tools and methodologies.
• Excellent analytical and problem-solving skills.
• Demonstrated leadership and mentoring experience.
• Exceptional communication with diverse audiences.
• Attention to detail and ability to manage multiple projects.

Responsibilities

• Develop project plans and execute to achieve goals.
• Lead cross-functional teams to implement activities.
• Collaborate with stakeholders to define scope.
• Mentor team members and foster excellence.
• Develop project reports for stakeholders.
• Stay updated on industry trends to integrate best practices.
• Contribute to organizational growth through leadership.

Skills

Project management

Global clinical trials

Leadership

Stakeholder management

Communication

Analytical skills

Education

Bachelor's or Master's in PM/ Business

Tools

PM tools

Job description

ICON is seeking a Senior Clinical Project Manager to join our Internal Medicine team. This remote role in the United States focuses on leading and delivering complex clinical projects across global sites.

You will develop plans, mentor teams, collaborate with stakeholders, and drive documentation and reporting to stakeholders. A strong background in pharma/biotech and excellent communication are essential.