Location
Paris (75) | France
Job description
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:
- Project Planning: Developing project plans, timelines, and budgets in alignment with study protocols and regulatory requirements.
- Regulatory Compliance: Ensuring adherence to relevant regulations, guidelines, and Good Clinical Practice (GCP) standards throughout the project lifecycle.
- Risk Management: Identifying potential risks to project timelines, budgets, and data integrity, and implementing strategies to mitigate these risks.
- Vendor Management: Selecting, contracting, and managing relationships with external vendors such as clinical research organizations (CROs), laboratories, and suppliers.
- Protocol Oversight: Collaborating with clinical investigators to ensure protocol compliance and proper conduct of clinical trials.
- Data Management: Overseeing data collection, monitoring data quality, and ensuring timely and accurate data analysis and reporting.
- Communication: Facilitating communication among project team members, sponsors, regulatory authorities, and other relevant stakeholders.
- 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
Job tags
Salary
50k € a 60k €/an
