Clinical Project Manager

Job Title: Clinical Project Manager
Location: Paris (Hybrid working)
Salary: €50,000 - €60,000

Position Overview:

Albion Rye Associates are looking for a talented Clinical Project Manager ideally with Phase II & III experience. You will be joining one of our key global clients working across my clients entire portfolio.

This is a unique opportunity to add immense value in a high-growth, evolving, and collaborative environment where your work will directly impact company success.

Their responsibilities include:

1. Project Planning: Developing project plans, timelines, and budgets in alignment with study protocols and regulatory requirements.
2. Regulatory Compliance: Ensuring adherence to relevant regulations, guidelines, and Good Clinical Practice (GCP) standards throughout the project lifecycle.
3. Risk Management: Identifying potential risks to project timelines, budgets, and data integrity, and implementing strategies to mitigate these risks.
4. Vendor Management: Selecting, contracting, and managing relationships with external vendors such as clinical research organizations (CROs), laboratories, and suppliers.
5. Protocol Oversight: Collaborating with clinical investigators to ensure protocol compliance and proper conduct of clinical trials.
6. Data Management: Overseeing data collection, monitoring data quality, and ensuring timely and accurate data analysis and reporting.
7. Communication: Facilitating communication among project team members, sponsors, regulatory authorities, and other relevant stakeholders.
8. Budget and Resource Management: Monitoring project expenses, managing resource allocation, and ensuring efficient use of project resources.

Qualifications:

• Minimum 5 years of experience as in Clinical Trials and Clinical Research
• Fluent in English & French
• Prior experience working in a CRO, Pharmaceutical or Biotech