Consultant Senior Clinical Project Manager
EPM Scientific are currently partnered with a Pharmaceutical company who are seeking a Consultant Senior Clinical Project Manager to support their existing Hepatology programs. See a short summary below:
Contract Conditions:
- Start date: ASAP
- Location: United States (Remote)
- Contract: 0.8 - 1 FTE, 12-Month Contract
- Language: English
- Project: Hepatology - Global Trial
Key Responsibilities:
- Lead and oversee global clinical trial sites, ensuring compliance with GCP, protocol, and regulatory requirements.
- Serve as the primary point of contact for internal and external stakeholders, supporting site initiation, monitoring, and close-out activities.
- Ensure timely and accurate documentation, data collection, and reporting in line with project timelines.
- Collaborate with cross-functional teams including CRAs, Medical Monitors, Regulatory Affairs, and Data Management.
- Contribute to risk-based monitoring strategies and support audit readiness.
Requirements:
- Strong (5+ years preferred) experience in clinical project management, ideally in Hepatology or related therapeutic areas.
- Strong knowledge of ICH-GCP and FDA regulatory environment.
- Proven ability to work independently and manage global clinical operations.
- Excellent communication and organizational skills.
If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.
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