לוח משרות דרושים רופאים ומנתחים משרה מלאה

About The Position:
Clinical Expertise: Serve as a primary medical resource within the company, providing clinical insights and expertise to inform product development decisions.
Medical Oversight: Provide medical oversight throughout the product development lifecycle, from concept ideation to regulatory approval and post-market surveillance.
Clinical strategy: Involve in the clinical strategy discussions and decisions for our AI clinical product, aligning with the company's overall vision and objectives.
Clinical Validation: Design and oversee clinical validation studies to demonstrate efficacy and utility of our product, collaborating with external clinical partners as needed.
Cross-functional Collaboration: Collaborate closely with interdisciplinary teams, including data science, engineering, product management, and regulatory affairs, to integrate medical considerations into product development
Hands-On clinical tasks: Lead and execute hands-on clinical tasks including mapping, clinical requirements definition, training sessions, and more
Customer-Facing responsibilities: Support sales and customer success through active participation in clinical discussions, assist in the implementation plans and executions.

Are you ready to make a difference in the world of healthcare?we are committed to pushing the boundaries of science to deliver life-saving medicines that transform patients' lives. As a Medical Advisor in the Cardio Vascular therapeutic area, you will play a pivotal role in shaping the performance of brands. You will be at the forefront of building scientific partnerships with Key External Experts (KEE) and healthcare professionals, driving strategic and educational medical affairs projects, and providing essential medical input to marketing, sales, and market access teams. This dynamic role combines office-based work with significant field presence, allowing you to continuously build robust scientific expertise and contribute to the medical therapeutic area strategy.

Accountabilities:
Conduct scientific exchange and collect customer insights:
-Stay up-to-date in TA knowledge through active monitoring of scientific literature, congress attendance, and interactions with Key External Experts (KEE).
Lead pre-launch medical strategy and initiatives to address current gaps.
Discuss key data sets with experts to identify patient pathways and treatment realities.
Build relationships with experts for advocacy development.
Brief speakers for scientific events.
Respond to unsolicited requests for information about unapproved products or uses.
Continuously improve impactful communication skills.
Interact with other Medical Advisors/MSLs and MAMs to exchange best practices.

Deliver Key medical leadership into the brand strategy:
Work in strategic partnership with Marketing and Market Access Department.
Provide high-quality scientific and medical input in Brand Teams and strategic projects.
Review and approve promotional material with thorough understanding of standards.
Develop and execute medical affairs projects according to budget and timelines.
Coach and support MSLs to ensure development and execution of MSL Action Plans.
Maintain top-notch robust scientific and medical expertise:
Keep track of relevant scientific literature in the TA.
Attend international and national scientific congresses.
Engage with KEE in the TA.
Ensure excellent up-to-date scientific knowledge among internal colleagues.
Support Clinical operations in site selection.

Manage scientific partnerships with KEE:
Manage Externally Sponsored Research.
Follow-up on grants/chairs/scientific sponsorings with KEE.
Organize and lead meetings with KEE for input on data sets or projects.
Be compliant:
Successfully complete all training requirements.
Comply with external regulations & internal policies.

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.

We are looking for a Medical writer and Regulatory Affairs associate.
Roles and Responsibilities:
Work with clinical teams and clients to understand the nature of the scientific work that they will be covering.
Assess data or products using medical expertise, and quickly develop expertise in new areas as needed for their writing.
Help to write studies for submissions to the FDA. The writing is also used in publications or medical journals, or for internal company use.
Comprehensive writing of clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis and integrated summaries from raw data.
Prepare abstracts, scientific exhibits, posters and verbal presentations.
Help with develop and write pharmaceutical training materials, eLearning content, video scripts, magazine articles, and presentations to be used by a variety of audiences.
Conduct comprehensive literature searches to enhance background understanding, and evaluate and analyze the information which will be written about.
Provide responses to regulatory agencies regarding product information or issues.
Maintain current knowledge of relevant regulations, including proposed and final rules. Help in manage activities such as audits, regulatory agency inspections etc.
Participate in the development or implementation of clinical trial protocols. Preparation and submission of regulatory agency applications, reports, or correspondence.
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products.
Primary function of the position
Clinical scientific knowledge and writing skills to effectively and clearly communicate medical science information in writing. Generally, focus on either scientific medical writing, which includes clinical studies, and regulatory documents, scientific articles or marketing medical writing. Experience in regulatory aspects (RA), help to lead regulatory strategy and provide ongoing regulatory input.