לוח משרות דרושים ניהול ברפואה משרה מלאה

Medison offers hope to patients suffering from rare and severe diseases, by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve. We are a dynamic, fast-paced company, operating in over 25 countries on 5 continents. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us! The Medical Affairs Manager (MAM) is a key member of the Country medical team and represents a primarily field and customer focused role, enabling medically oriented interaction with internal and external stakeholders on the basis of individual contacts, educational events and medical projects. The MAM will provide expert medical support including educating the local sales and marketing team as needed. They will be an expert on the disease areas under their responsibility and will ensure their knowledge is current and thorough. Supports the Country/ Cluster Medical Head in creating the Medical Customer Engagement Strategy and the Medical Affairs project-plan for Medical Launch Excellence and successful Life Cycle Management fully in line with brand strategies and company objectives to meet the predefined targets of the Affiliate medical affairs department. The MAM reports to the Country/ Cluster Medical Head.
Responsibilities:
* Works closely with the Country Medical Head and Commercial team to establish a medical footprint in the Country.
* Communicates with different internal functions to synchronize touchpoints with HCPs for optimized customer experience
* Establishes, develops and manages collaborative relationships with key external medical experts and opinion leaders related to any current and future disease areas relevant for the company and develops a deep understanding of their needs.
* Contributes to the generation and communication of complex scientific information, communicating scientific data related to current and future products to all stakeholders.
* Reviews and approves promotional and educational material, coordinates such reviews and approvals with MA representatives and in accordance with Medison SOPs.
* Drives disease awareness in providing external medical disease education and setting up local scientific programs, such as symposia, regional advisory boards, or scientific meetings in accordance with the respective disease plans and in line with current compliance guidelines.
* Coordinates and pro-actively contributes to all pre-launch and life cycle activities for current products and potential pipeline products in the country.
* Provides medical support and medical information on unsolicited HCP requests related to any products in accordance with the relevant processes and local regulations.
* Is an active member of scientific and educational interactions with therapeutic specialists on diagnostic and clinically relevant aspects of any therapeutic areas worked in.
* Locally facilitates any patient access programs (EAP) to address high unmet medical needs.
* Collects competitive intelligence and market insights within the region on diagnostic methods and treatment paradigms of any relevant therapeutic areas.
* Communicates KOL insights that influence the development of brand plans and strategies.
* Pro-actively supports internal medical knowledge development and provides internal training for MSLs, sales and other functions on any relevant disease and product related aspects, in alignment with guidance

We offer hope to patients suffering from rare and severe diseases, by forming partnerships with emerging biotech companies to accelerate access to highly innovative therapies in international markets. As the creator and leader of the global partnership category in the pharma industry, we strive to be Always Ahead, and work relentlessly to bring therapy to patients in need, no matter where they live. Our values are at the core of every action we take, and we are committed to going above and beyond for the benefit of the patients we serve. We are a dynamic, fast-paced company. We are looking for out-of-the-box thinkers, people who are passionate, caring, agile and adaptive, to join us on our mission. If you are looking to make a difference in people's lives, we invite you to join us! The Medical Science Liaison (MSL) is a key member of the country medical team and represents a primarily field and customer focused role, enabling medically oriented interaction with internal and external stakeholders on the basis of individual contacts, educational events and medical projects. They will be an expert on the disease areas under their responsibility and will ensure their knowledge is current and thorough. The MSL implements the medical strategy locally and supports the generation and communication of scientific information. They act as the primary point of contact for a set of HCPs (incl. KOLs) and ensure good communication with sales and market access colleagues. The MSL reports to the Medical team lead.
Responsibilities:
* Works closely with the Medical Lead and Commercial team to establish a medical footprint in the Country.
* Establishes, develops, and manages collaborative relationships with key external medical experts and opinion leaders related to any current and future disease areas relevant for the company and develops a deep understanding of their needs.
* Contributes to the generation and communication of complex scientific information, communicating scientific data related to current and future products to all stakeholders.
* Drives disease awareness in providing external medical disease education and setting up local scientific programs, such as symposia, regional advisory boards, or scientific meetings in accordance with the respective disease plans and in line with current compliance guidelines.
* Coordinates and pro-actively contributes to all pre-launch and life cycle activities for current products and potential pipeline products in the country.
* Provides medical support and medical information on unsolicited HCP requests related to any products in accordance with the relevant processes and local regulations.
*  Is an active member of scientific and educational interactions with therapeutic specialists on diagnostic and clinically relevant aspects of any therapeutic areas worked in.
* Locally facilitates any patient access programs (EAP) to address high unmet medical needs.
* Collects competitive intelligence and market insights within the region on diagnostic methods and treatment paradigms of any relevant therapeutic areas.
* Communicates KOL insights that influence the development of brand plans and strategies.
* Pro-actively supports internal medical knowledge development and provides internal training for sales and other functions on any relevant disease and product related aspects, in alignment with guidance from the Medical Affairs Director EPM
* Manages/supports local aspects of investigator-initiated trials or other research projects in accordance with respective local laws and with us and MA SOPs
* Ensures that all activities required by pharmacovigilance and risk management are planned, set- up and pursued in accordance with respective local laws and with our SOPs
* Ensures legal excellence and compliance in all medical activities as per company SOPs and local regulations.

required Medical Lead
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

About the role:
we are a fast-growing, global leader in energy-based solutions for Aesthetics and Eye-Care. We are based in Yokneam, Israel (with offices in Tel-Aviv) with a strong business performance worldwide.
We are looking for a Clinical Manager for the Aesthetics Business Unit, which includes a broad portfolio of leading solutions in the market as well as an exciting innovation pipeline. The Clinical Manager will be responsible for pre and post-market activities for the assigned platform including: clinical requirements guiding design input, pre-clinical testing, clinical input to regulatory submissions, market conditioning for new solutions, post-market evidence generation and KOL development. The individual will serve as a major pillar in building relationships with global KOLs and demonstrating the clinical value and benefits of the solutions.
Key responsibilities:
Develop and manage clinical project plan, timelines, and budgets end to end; clinical research, through pre-clinical evaluations, clinical trials and publications, to user guidelines and post-market evidence generation.
Form and cultivate strong collaborative relationships with cross-functional partners in R&D, product, marketing, and regional teams
Coordinate internal cross-functional teams, as well as external clinical research associates, data managers, and biostatisticians
Oversee the execution of clinical studies, ensuring adherence to protocols and regulatory requirements
Lead the clinical input and support for key regulatory submissions and processes: regulatory submission clinical input, clinical validations, CER, CDP, CEP and more
Support marketing/commercial activities from the scientific/medical point of view: review and input to marketing collateral, develop white papers, active participation in scientific meetings and more
Communicate project status to stakeholders and provide updates on milestones and deliverables
Identify potential risks and implement mitigation strategies to ensure project success.

Are you passionate about leading a team to success? Do you want to play a pivotal role in shaping the future of healthcare? We are seeking a dedicated Medical Science Liaison (MSL) Lead to join our team in Israel and drive our scientific communication strategy. If this sounds like your next career move, read more and apply today for a life-changing opportunity!
The Position
As our MSL Lead you will be responsible for guiding and developing the MSL team to effectively execute the field medical affairs strategy initiatives, ensure alignment with commercial objectives, and enhance scientific partnership with healthcare professionals. You will be reporting directly to Head of Medical Affairs.
Additionally, you will:
Lead, mentor, and develop the MSL team to ensure strong performance, professional growth, and alignment with company goals.
Oversee and ensure adherence to standardized MSL processes and compliance with industry regulations.
Collaborate cross-functionally to design and execute medical education initiatives that strengthen scientific understanding among healthcare professionals.
Develop and manage ongoing training programs to support continuous learning and promote a high-performance team culture.

A day in the Life:
Manages all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, may assume Clinical Study Manager (CSM) responsibilities on small and/or less complex projects.
Develops clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan.
Contributes to the development of the Master Action Plan (MAP) for providing clinical related documents.
Ensures timely set up, organization, content and quality of the relevant sections of the Trial Master File (local and central).
May participate in the design and development of CRFs, CRF guidelines, patient informed consent templates and other protocol specific documents as required.
Collaborates with the project manager to prepare, organize, and present at client meetings, including bid defense and hand-off meetings.
Collaborates with the clinical team and other departments as needed to meet deliverables of the project.
Regularly communicates with the team and leads team meetings to ensure that timelines, resources, interactions, and quality are maintained.
Responsible for the implementation and training of standardized clinical monitoring processes within the study and according to corporate standard policies.
Responsible for the timely archiving of documents and study materials for the department.
Ensures achievement of the final clinical deliverable within the contractual time period specified by preparing and monitoring clinical activity timelines and metrics, providing status updates to the project manager, regularly reviewing projects using tracking and management tools, implementing recovery actions, reviewing monitoring visit reports, and managing CRF collection and query resolution.
Continuously monitors or co-monitors clinical trials to assess performance and ensure contractual obligations are met. In smaller regions, may routinely conduct Accompanied Field Visits (AFVs) and be accountable for project financials.
May communicate with study sites regarding issues such as protocol, patient participation, case report form completion and other study-related issues.
May coordinate all start-up activities and ensures that timely ethics committee and regulatory submissions (if appropriate) are addressed.

We are an innovative global healthcare company that helps the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses a year. Across different countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.

Medical Science Liaison is the extension of the medical function in the field. They build and develop enduring win-win' relationships with healthcare professionals and institutions, creating constructive partnerships with internal and external stakeholders to generate insights. MSL is executing the field medical activities that are aligned and integrated to the overall medical strategy within the Vaccines CSE MCO.

Main responsibilities:

Be the trusted scientific partner to key external experts by conducting timely, appropriate and frequent scientific exchanges to enhance the understanding of the scientific and medical value of our products.
Actively engages with appropriate stakeholders on medical, clinical, epidemiologic, and scientific topics during an one-on-one interactions and group settings, to advance their understanding of the disease by sharing information and answering questions based on approved material within Regulatory guidelines.
Effectively utilizes the Scientific Engagement Model to plan territory and individual stakeholder (Key Opinion Leaders, payers, HCP etc.) medical strategy and engagement interaction plans consistent with the Field Base Medical Activity Plan and medical function priorities.
Supporting external lecturers in delivering balanced, non-promotional knowledge about therapeutic areas and our products.
Participating in the development and implementation of educational programs to improve the daily practice of healthcare professionals.
Organize and run external scientific events for our company about relevant disease or therapeutic topics.
Attending conferences and scientific symposia in the relevant therapeutic area.
Provide scientific support to the commercial team as necessary.
Collect key insights about the market, competitors, therapies, and customers.
Actively participate in on-going capabilities building sessions to improve medical knowledge, soft skills, and technical skills