Website Alsinova
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 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.
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.
Alsinova
Alsinova is setting new standards for CROs by integrating multidisciplinary expertise with advanced technology. Alsinova offers a complete CRO solution, providing innovative, customised solutions in various life science segments: pharmaceuticals, biotechnology, medical devices, cosmetics, agri-food, veterinary and healthcare institutions.
Alsinova is the subsidiary of the Astek Group, a global player in engineering and technology consulting. Since its creation, the Group has based its development on a strong culture of entrepreneurship and innovation, and on the support and skills development of its 10.000 employees who are committed every day to promoting combination of digital technologies and complex systems engineering.
Join a Group rapidly developing in France and around the world, with a turnover of 705 M€ in 2024.
More on the Group on our websites https://alsinova.com and https://astek.net.
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.