דרושים » רפואה ופארמה » In house Senior Pathologist

We are hiring a senior data scientist to join Nucleai’s data science team. A cancer patient wants to know that their diagnosis and treatment are determined with the greatest precision and preferably using the most advanced technology. At Nucleai, we bring cancer patients cutting-edge AI-based technology by improving biopsy interpretation with machine learning and creating novel precision medicine technology. Come join our team of experienced AI engineers and world-renowned clinicians, and help us make a difference. At Nucleai, we believe that talents are our most valued asset, and as such, hiring the right people is one of our most strategic missions.
Position Overview The data science team provides the bottom line to our customers – which patients are the best fit for a cancer treatment and what is the chance of success. We do it by analyzing medical images and clinical data, researching spatial features, developing predictive models and applying statistical methods to evaluate the results. We work together with subject-matter experts, from medical doctors to software engineers, to leverage computer vision, focus on the most promising biological hypotheses and to productionize our capabilities.
Responsibilities:
* Independently lead the data science perspective in any project or assignment – from data mining, through developing new algorithms, to analyzing results and providing professional insights and guidelines.
* Contribute to the team's internal codebase with high-quality code and development standards.
* Augment our knowledge and best practices, adopt relevant SOTA data science methods and practices.
* Work closely with medical doctors, product and project managers, research scientists and software developers to focus your efforts, build new capabilities and provide value to your colleagues and our 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.

We are looking for a Clinical Trial Coord.
As a Clinical Trial Coordinator, you will provide administrative and technical support to the Project Team.
You will support audit readiness by ensuring files are reviewed on schedule detailed in the organization's WPD and department guidance document.