לוח משרות דרושים רופאים ומנתחים משרה מלאה, לחיפוש זה נמצאו 34 משרות

The Medical Manager in the field of Gyneco-Oncology, holds primary responsibility within the country for the development and execution of the Medical Affairs strategic plans and, is expected to spend up to 50% of their time in external engagements.

Key responsibilities include cross-functional strategy collaboration and execution, building trust with the medical/scientific community, facilitating peer-to-peer medical and scientific exchange, and providing asset issue resolution support.

Responsibilities and Primary Activities

Strategic and Tactical Leadership

Consolidates actionable medical insights to inform company strategies
Translates Global Medical Goals and Strategies into tactics and solutions that support optimal scientific exchange aimed at helping improve patient outcomes and enhancing access
Supports execution of and quickly adapts tactical plans to local business realities
Follows up on Investigator-Initiated Study (IIS) proposals aligned with Our Company ISS Program areas of interest
Collaborates with our research laboratories/Global Clinical Trial Operations (GCTO) personnel to identify potential investigators for our clinical development programs
In collaboration with colleagues, facilitates the delivery of data generation activities (phases I-IV), including the identification of suitable research projects, research centers, investigators, and innovative methods to generate data
Provides non-promotional, balanced, and reliable scientific information following company standards and local regulations


Medical and Scientific Leadership

Brings the local scientific and healthcare environment perspective to the Regional Medical Affairs team
Communicates scientific and business needs appropriately and effectively across internal and external stakeholders
Builds trust with the external scientific community via peer-to-peer scientific exchange, research, and educational collaborations, as well as interactions with scientific societies, health organizations, publications, etc.
Provides therapeutic/functional training to assigned teams and affiliate functions
Develops and executes country medical educational programs and symposia
Leads country advisory boards and expert input forums
Participates in and contributes to professional organizations and academic/regulatory working teams


Regulatory and Market Access Support

Collaborates and leads resolution of regulatory, public relations, compliance, and other asset issues
Supports the resolution of asset safety or quality issues (i.e., contributes content and strategy in regulatory responses and interactions, risk management planning, and implementation)
Provides access support as needed (e.g., health technology assessment, pre-license patient access, reimbursement dossier)

We are looking for an Associate Director, Medical Affairs position to be responsible for the medical affairs team in Israel, responsible for Oncology. The Associate Medical Director is a non-promotional role which leads a team of Medical Affairs Manager/MSLs who engage in scientific exchange with healthcare professionals and scientists (HCPs), with emphasis on regional and national scientific leaders and key decision makers.

The Associate Medical Director is responsible for the teams scientific activities and performance. Although the Medical Advisor is the owner of the strategic plan, the Associate Medical Director may also provide input and insight based on his/her team interaction with their SLs and other stakeholders engagements into the Medical Affairs strategy and ensure that it translates into concrete engagement (action) plans in the field.

The Associate Medical Director may also represent us in a range of local, national and international non-promotional Medical Affairs activities.





The job duties include the following:

Budget Planning and Resource Management.
Hires, manages, coaches and develops a group of Medical Affairs Managers/MSLs assigned to his/her therapeutic areas to ensure the highest quality scientific exchange in alignment with the Medical Affairs plan.
Provides input into the therapeutic area Medical strategy led by the local Medical Affairs Managers.
Ensures that there is adequate and compliant cross-functional collaboration between the Medical Affairs Managers/MSLs and internal stakeholders.
Organizes regular team meetings for relevant trainings, sharing of best practices, reinforcing on compliance matters and discuss therapeutic area strategies.
Develop his/her Medical affairs managers/MSLs functional and scientific skills.
Establishes the annual performance objectives for his/her team.
Conducts mid-year and year-end reviews of team performance.
Develops and maintains up-to date scientific knowledge around relevant disease areas, products within those areas and research methodologies.
Ensure optimal scientific leader management and support
Develop medical strategy (including the Medical Affairs plan, MAPs)
Align medical strategy with business unit/franchise-needs with marketing
Responsible for the creation and timely execution of all Medical activities in his areas of responsibility including medical education, data generation activities etc...
Responsible for close follow ups on all systems updates of the activities under his responsibility.
Review and approve s MSL plans.
Collaborate with GCTO and Market access around new products.
Ensures that all Medical Affairs Managers/MSLs perform their duties in alignment with company SOPs/Guidelines and local laws and regulations.

Digital and Medical Modernization Lead, reports to the Country Medical Director.

This role operationalizes the V&I digital data and innovation and the Medical Modernization (MM) strategy locally across applicable therapeutic areas and drives digital scientific engagement for all Therapeutic Areas (TA) in Israel. This highly cross-functional role works closely with local and global Medical Affairs, as well as Digital, Data & IT, CRM/Data Analytics, Legal and Compliance stakeholders, to support the Medical Affairs teams digital transformation and embed digitalization into current ways of working and future strategic development. The role is primarily responsible for identifying, developing and implementing foundational digital and data analytics capabilities that translate into an innovative, efficient and competitive Medical Affairs organization. The Lead builds and engages the TA-specific digital Scientific Leader (SL) roster in close alignment with the Country Medical Advisors of that TA, executes data-driven, omnichannel scientific engagement projects, and measures impact using Veeva CRM/VVMC and analytics dashboards in collaboration with the Medical Modernization Center of Excellence. The Digital Lead adapts global/regional scientific content for local use in compliance with policy and SOPs, decides with the Country Medical Director and Medical Advisors where to use the content, enables country medical teams to transition to omnichannel engagement of priority SLs/KDMs, provides guidance and support to help local medical team to master required capabilities, and feeds insights and results to inform scaling decisions.

At a country level, the Digital Lead partners with the local Medical Affairs Team working closely under the CMD sponsorship, Digital and IT teams (COD), Commercial Business Unit colleagues, and legal/compliance experts to ensure successful execution of the planned activities.

The Digital Lead will build a bidirectional communication between the region and cluster/country, share and scale best practices, and modernize the way medical affairs teams work in your country and in the region.

The Digital Lead function is critical in our change management efforts by communicating and supporting new ways of working, and inspiring others to adopt innovative ways of working as we shape and transform our V&I engagement strategy, drive MM efforts and transformational change within medical affairs, fostering a culture of continuous improvement to achieve long term success.

The Medical Manager holds primary responsibility within the country for the development and execution of the Medical Affairs strategic plans and, is expected to spend up to 50% of their time in external engagements.

Key responsibilities include cross-functional strategy collaboration and execution, building trust with the medical/scientific community, facilitating peer-to-peer medical and scientific exchange, and providing asset issue resolution support.

Responsibilities and Primary Activities

Strategic and Tactical Leadership

Consolidates actionable medical insights to inform company strategies
Translates Global Medical Goals and Strategies into tactics and solutions that support optimal scientific exchange aimed at helping improve patient outcomes and enhancing access
Supports execution of and quickly adapts tactical plans to local business realities
Follows up on Investigator-Initiated Study (IIS) proposals aligned with Our Company ISS Program areas of interest
Collaborates with our research laboratories/Global Clinical Trial Operations (GCTO) personnel to identify potential investigators for our clinical development programs
In collaboration with colleagues, facilitates the delivery of data generation activities (phases I-IV), including the identification of suitable research projects, research centers, investigators, and innovative methods to generate data
Provides non-promotional, balanced, and reliable scientific information following company standards and local regulations

As a Digital Medical Advisor, you'll be at the forefront of how we communicate science in the digital age. You'll develop and execute medical strategies that strengthen our digital scientific communication and drive meaningful engagement with Digital Opinion Leaders (DOLs) across Israel.

Your responsibilities will include:

Driving comprehensive DOL engagement strategies from end-to-end - identifying, assessing, and cultivating relationships with key Digital Opinion Leaders to amplify scientific dialogue and foster compliant advocacy
Developing tailored content, resources, and specialized workshops that resonate with digital audiences and advance scientific understanding
Preparing, medically reviewing, and disseminating all corporate medical communications across digital platforms, ensuring scientific accuracy and regulatory compliance
Creating planned medical scientific journeys for all relevant audiences, translating complex scientific content into impactful digital formats
Collaborating with Marketing, Sales, Medical, Compliance, and Customer Excellence teams to align strategy, prioritize initiatives, and execute scientifically accurate, impact-driven programs
Engaging with healthcare professionals and DOLs, to gather insights, co-create content, and ensure clinical relevance
Driving innovation in digital engagement by adopting new channels and methodologies that support our digital-first Medical Affairs model

As our new Patient Activation Medical Advisor, you will develop, review and execute medical strategies that strengthen patient engagement across our therapy areas. Working at the intersection of science, communication and compliance, you will ensure that every patient-facing initiative is scientifically robust, ethically sound, and genuinely useful to the people we serve.

Your day-to-day responsibilities will include:

Collaborating closely with Marketing and Customer Excellence to strategically develop and medically review patient-facing materials, ensuring scientific accuracy, compliance, and clarity
Organising and supporting impactful patient activities and educational initiatives that enhance patient knowledge, support and outcomes
Translating medical and scientific evidence into patient activation concepts, and drafting or co-creating patient materials in line with approved product information
Partnering with Compliance, Legal and internal governance functions to ensure patient communications meet regulatory and ethical standards, and are updated as evidence and requirements evolve
Aligning cross-functionally with Marketing, Sales, Medical, Compliance and Customer Excellence to prioritise initiatives and execute scientifically accurate, impact-driven programmes
Adapting patient engagement content and medical strategy inputs to evolving evidence, patient needs and internal learnings - maintaining scientific rigor at every step

The Medical Director for the Hematology-Oncology Center of Excellence provides strategic medical and scientific subject matter input to us in this therapeutic area informed by their training, experience and expertise. The activity of the medical director includes but is not necessarily limited to early engagement with potential customers, proposal development in response to RFPs, participation in client proposal bid-defense meetings, support at scientific conferences, participation in thought leadership activities, contribution as needed to the formulation of clinical development plans, providing medical director and subject matter expertise as a consultant throughout the research and development lifecycle and the duration of clinical trials, and engagement with colleagues as an internal reference SME for hematology-oncology. Greater independence is expected to be demonstrated over time for medical director activities under the supervision of the therapeutic area head and leadership team.

Essential Functions

Work independently under the supervision (direct or indirect) of the Hematology-Oncology Center of Excellence Head and COE Leadership team.

Provide scientific and clinical advice to internal stakeholders developing proposals, including but not limited to: protocol design/ clinical development plan, insights on mechanism of action of the investigational product, mining data to address important clinical questions relevant to the study, reviewing protocol for scientific/regulatory soundness and feasibility, identification of target site and principle investigator profiles, anticipated patient recruitment, standards of care and competitive landscape.

Maintain awareness of latest literature to keep abreast of scientific progress in hematology and oncology.