We are looking for a Senior Pathologist to join our team.
As an part-time \ in-house pathologist, you will work closely with our R&D team on new applications for our cancer diagnostics platform as we expand it to additional tissues and indications, acting as subject matter expert and advising on all clinical matters.
You will further work with our AI experts, scientific researchers and other pathologists on tasks such as:
Annotate (mark and label) various cell types and structures in whole-slide images
Analysis of algorithmic performance and clinical data
Design and execution of clinical research and case studies
Advise on improvements to our platform, workflow and user-interface
Writing clinical, scientific and other pathology-related papers
Help the commercial team engage physicians and improve adoption of our solution by customers.

We are looking for a Clinical Research Associate (CRA) to join our Compliance and Regulatory Affairs (RA) team. Compliance and RA team is responsible for the companys clinical and regulatory activities, quality management systems, and for ensuring compliance with applicable standards.

The team plays a central role in both pre-market and post-market activities. The CRA will play an important role, working with clinical sites, ensuring successful management of clinical activities, and performing assigned monitoring activities throughout the clinical trial lifecycle.



Your responsibilities will include:

Managing global clinical trials at multiple clinical sites, taking part in planning clinical studies, defining clinical protocols, and supporting regulatory documentation.
Collaborating with multiple stakeholders to ensure successful, rigorous, and timely studies.
Proactively managing clinical study processes and monitoring activities. Overseeing and supervising clinical operations to ensure activities are carried in accordance with applicable regulatory requirements and guidelines.
Maintaining strong relationships with external experts to ensure effective execution of clinical studies and research projects.
Taking part in defining and approving clinical study protocols and plans, IRB submission documents, CRFs, and clinical study reports.
Facilitating team training per study protocols and supporting regulatory submission and documentation.