Clinical Project Manager - Montréal, Canada (F/M)

What we will accomplish together: Alsinova is looking for an experienced expert in clinical research and healthcare management to act as a Clinical Project Manager. Join our developing team in Canada, and quickly grow your potential for the future. Your mission (should you decide to accept it): Responsibilities include managing and coordinating various aspects of clinical trials. Your daily activities will be:Strategic Planning:

• Develop comprehensive plans for initiating, executing, and completing clinical trials, aligning them with project goals and timelines. Study Documents Development:
• Contribute to creating and refining study protocols, outlining methodology, objectives as well as the ICF, the eCRF and any other study related documents. Risk Management:
• Identify and manage risks associated with clinical trials and make recommendations
• Ensure compliance with regulatory standards, timelines, and budgets. Team Leadership:
• Work hand to hand with Client European Clinical Head and extraordinary local support.
• Supervise clinical research associates and documentation specialists.
• Train team members on daily project operations. Vendor Management:
• Manage vendors to guarantee patient safety, contract adherence, and data integrity and financial engagement.
• Act as the primary contact for vendors. Documentation and Communication:
• Prepare and review documents related to clinical projects (contracts, vendor budgets, annual reports).
• Facilitate effective communication between research teams, sponsors, and regulatory authorities. Data Analysis and Reporting:
• Participate in data analysis, summary, and reporting for regulatory requirements.

You:

• You have at least a Master's degree in a scientific discipline (biology, biomedical sciences, pharmacy) or equivalent.
• You have 5-8 years' experience in clinical operations (including field follow-up) and CRO and supplier management is required.
• You have previous experience of Phase I/II clinical trials in the field of immuno-oncology.
• You have knowledge of ICH GCP and other legislation applicable to clinical studies.
• You are familiar with clinical study management tools and systems (eCRF databases).
• You are able to work independently and adapt to rapidly changing situations and needs.
• Strong commitment to high-quality work.
• You are keen to join a fast-growing, fast-paced biotech company.
• Other personal qualities: organized, pragmatic, flexible, persistent, open-minded, results-oriented.

Our Benefits Joining Astek means choosing:

• an experience accelerator, where every assignment is an opportunity to progress
• access to a multitude of technically exciting projects for our clients as well as internally
• individualized, local support for a tailored career path
• continuous learning, thanks to our internal training academy
• a friendly and inclusive work environment, supported by #TopEmployer2025 certified HR practices Let's move forward.