Project Manager
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Job Description
Project Manager overseeing cardiovascular clinical trials for a real-world-evidence CRO. Coordinating sponsors, investigators, vendors, budgets, risks, regulatory compliance, and clinical data integrity.
Responsibilities:
- Plan, coordinate, and oversee all stages of clinical trials, including project planning, budgeting, resource allocation, execution, and closeout
- Ensure clinical trials comply with protocols, SOPs, GCP, and applicable regulatory requirements
- Serve as the primary contact for sponsors, investigators, and stakeholders
- Provide timely and accurate project updates
- Identify project risks and develop and implement mitigation strategies
- Collaborate with internal teams and external vendors to meet project goals
- Oversee data management activities and ensure clinical trial data accuracy and integrity
- Conduct regular project meetings and document and follow up on actions and decisions
- Prepare and present project reports to senior management and stakeholders
- Complete all mandatory training on time and according to company requirements
Requirements:
- Bachelor’s degree in a life science or related field
- Master’s degree or relevant certification preferred
- Minimum of 5 years of experience in clinical project management within a Contract Research Organization (CRO), biotech, or pharmaceutical company
- In-depth understanding of clinical trials, including planning, execution, and regulatory requirements
- Strong project management skills, with the ability to manage multiple projects simultaneously
- Excellent communication and interpersonal skills
- Strong problem-solving skills and the ability to adapt to changing circumstances
- Proficiency in project management software and other relevant tools
- Must be authorized to work in the United States; employer participates in E-Verify
Benefits:
- Fully remote position
- Occasional domestic travel for company meetings, audits, etc.
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