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.

Strategic Planning Your daily activities will be:

• 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.

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.

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