Project Manager (Clinical Research)

Location: Fully remote within the United States of America; occasional domestic travel may be required for company meetings and audits.

Company

hirify.global is a full-service cardiovascular contract research organization powered by real-world evidence and a network of physicians and research institutions.

What you will do

• Plan, coordinate, and oversee clinical trials from project planning and budgeting through execution and closeout.
• Ensure compliance with protocols, standard operating procedures, good clinical practice, and applicable regulatory requirements.
• Act as the primary liaison for sponsors, investigators, internal teams, and external vendors.
• Identify project risks, develop mitigation strategies, and track project progress and decisions.
• Oversee clinical trial data management and support data accuracy and integrity.
• Prepare project updates and reports for senior management and stakeholders.

Requirements

• Bachelor’s degree in life science or a related field, or an equivalent combination of education and experience.
• At least 5 years of clinical project management experience within a CRO, biotech, or pharmaceutical company.
• In-depth knowledge of clinical trial planning, execution, and regulatory requirements.
• Strong project management, communication, interpersonal, problem-solving, and adaptability skills.
• Ability to manage multiple projects simultaneously and proficiency with project management software.
• Authorization to work in the United States is required; employment eligibility is verified through E-Verify.

Nice to have

• Master’s degree or relevant certification.

Culture & Benefits

• Fully remote work within the United States.
• Occasional domestic travel for company meetings and audits.
• Work within a collaborative clinical research environment focused on cardiovascular expertise and real-world evidence.