לוח משרות דרושים רפואה ופארמה בתל אביב יפו

Were a mission-driven leader in medical technology and solutions with a legacy of integrity and innovation. Work with us to incentivize better patient care, and partner across the industry to make healthcare more affordable and accessible. Be a part of a community of experts committed to ensuring quality, affordable healthcare worldwide.

We are hiring a Reimbursement & Market Access Analyst to join our team in Israel. The team utilizes in-depth knowledge of the Israeli healthcare system, as well as breadth of experience across multiple disciplines while partnering with external and internal stakeholders to drive complex processes to expend patients' access to Medtronic's therapies.
A Day in the Life
Assist executing of Israel's Reimbursement, Market Access and Health economics strategies to secure optimal reimbursement and funding for designated therapies.
Collaborate with stakeholders to plan, collect and synthesize data to demonstrate clinical and economical value of Medtronic therapies.
Create awareness and educate key healthcare decision makers and payers to increase the acceptance, adoption and/or use of Medtronic therapies and products.
Provide education and training to key internal audiences within the region on key reimbursement, pricing and health economic product specific data and tools.
Support market development activities via generation of Israel specific economic data and support development and compilation of clinical evidence.

A 100% Tel-Avivian Pharmacy, dedicated to Medical Cannabis, located in the heart of the Florentin quarter - TLV's most vibrant and lively neighborhood.
We're looking for compassionate, knowledgeable certified pharmacists who are interested in taking part in the Israeli Medical cannabis retail industry, from a unique point of view.
We started the Pharmacy in order to disrupt the way medical cannabis is communicated and treated in the country. 
This position will sharpen your existing, and will further equip candidates with valuable skills, useful for their continued development as professionals in the field.
Reach out to us if you feel this is an interesting opportunity.

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. 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.