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.