Job Description
About the Role:
We are seeking a motivated and detail-oriented Associate Clinical Project Manager (ACPM) to support the planning, coordination, and execution of Phase 1 and 2a clinical trials at our commercial Phase 1 unit in West London. This hybrid role offers the opportunity to work both on-site and remotely, providing flexibility while contributing to cutting-edge early-phase research.
Key Responsibilities:
1. Assist in the day-to-day management of clinical trials, ensuring compliance with protocols, GCP, and regulatory requirements.
2. Coordinate with cross-functional teams including clinical operations, regulatory affairs, data management, and quality assurance.
3. Assist in the day-to-day management of clinical trials, ensuring compliance with protocols, GCP, and regulatory requirements.
4. Oversee and coordinate vendor activities, ensuring vendors deliver in accordance with project timelines, quality standards, and contractual obligations.
5. Support the preparation and maintenance of study documentation, timelines, and budgets.
6. Liaise with internal and external stakeholders to ensure smooth trial conduct.
7. Contribute to the development of study protocols, informed consent forms and other essential documents.
8. Perform ethics and regulatory submissions in the UK, ensuring timely and accurate complet...