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.