לוח משרות דרושים רפואה ופארמה כולל נסיעות לחו"ל

We are a growing medical technology company transforming patient lives through innovative incisionless surgery.
Our culture is as unique as our people, a diverse global team, with different ideas, skills, interests, and cultural backgrounds driven by our core values Our Patients, Integrity, Team, Quality and Innovation.
Our dedication to making a real impact on the lives of millions of people and paving the path to a bright future for healthcare, is what bonds us as a Team. We work together in a dynamic collaborative environment to deliver successfully while believing and driving a life-work balance philosophy that encourages our employees to do things that are meaningful outside of work. Every role is significant, your voice is heard, and your ideas are encouraged. We challenge and empower our people to be great at what they do while providing a flexible work environment.
Walking through our corridors, you will be inspired by stories of career journeys. We take pride in growing internal talent and encourage our employees to achieve their professional ambitions. With employees in Israel - Haifa and K. Ono, Miami and Dallas, Shanghai, Tokyo and Europe, we offer in each region competitive perks and benefits.
Do the most meaningful work of your career by joining us on our mission to transform tomorrows, today.
 
 
What you will be doing:
* Primary responsibility is centered on establishing a cohesive medical information function within medical affairs. Will develop subject matter expertise over time to serve as a point of contact for internal and external medical inquiries, providing accurate, balanced, and evidence-based responses.
* Develop, manage and update a searchable medical information database to ensure timely and compliant communication with external stakeholders.
* Craft standardized response letters (SRLs), FAQs, and custom responses for HCPs and internal teams
* Monitor and critically evaluate emerging scientific literature, congress presentations, and clinical trial updates in order to routinely update SRLs, FAQs etc.
* Will partner with MSLs to maintain a Real-Time medical insights and intelligence repository based on field interactions.
* Participate as a medical reviewer on promotional and non-promotional material review boards.
* Ensure that all content complies with applicable laws, industry codes (e.g., EFPIA, ABPI), and internal SOPs.
* Support medical training initiatives and provide scientific input at internal meetings and external events.
* Collaborate with key internal stakeholders including Regulatory Affairs, Marketing, Market Access, and Clinical Development.