Celerion is hiring a Clinical Project Manager to lead and manage clinical trials from initiation through close-out. You will be responsible for the successful delivery of projects on time, within budget, and to the required quality standards.
What You'll Do
- Develop and manage comprehensive project plans, timelines, and budgets for assigned clinical trials.
- Serve as the primary point of contact for clients, investigators, and internal cross-functional teams.
- Monitor study progress, identify risks, and implement mitigation strategies to ensure project goals are met.
- Oversee the preparation of study-related documents and ensure regulatory compliance.
- Lead study team meetings and provide regular status updates to stakeholders.
- Manage third-party vendor relationships and performance.
What We're Looking For
- Bachelor's degree in life sciences or a related field.
- 5+ years of direct experience in clinical project management within a CRO, pharmaceutical, or biotechnology setting.
- Proven track record of successfully managing full-cycle clinical trials (Phase I-IV).
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Strong financial acumen with experience managing project budgets and resources.
- Excellent communication, leadership, and problem-solving skills.
Work Mode
This is a fully remote position for candidates located within the United States.
Celerion is an equal opportunity employer.
