לוח משרות דרושים ניהול ברפואה בשרון, לחיפוש זה נמצאו 15 משרות

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


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)


Medical Information

Provides prompt medical information support (e.g., answering medical inquiries) to stakeholders and reviews approval of local response documents
Inclusive Mindset and Behavior

Demonstrates eagerness to contribute to an environment of belonging, inclusion, equity, and empowerment
Leads by example and serves as a role model for creating, leading and retaining a diverse and inclusive workforce

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.

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 Pharmacovigilance Associate and Country Safety Head Backup, you will support pharmacovigilance activities in Israel and serve as backup to the Country Safety Head and QPPV, ensuring continuous compliance with local and international pharmacovigilance regulations while maintaining the highest standards of patient safety.
Your key responsibilities will include monitoring diverse safety information sources to ensure timely detection and appropriate management of incoming pharmacovigilance data, assisting in the overall evaluation of pharmacovigilance information, and reporting safety related information to relevant stakeholders including Health Authorities. You will support local safety surveillance activities, including the management of safety signals and assessment of new safety information, and support to risk management activities.
You will serve as the designated backup to the Country Safety Head (CSH) and QPPV, ensuring continuity of pharmacovigilance operations and regulatory compliance during absences. In this capacity, you will maintain Israel's primary pharmacovigilance contact relationship with Health Authorities and provide support for strategic safety leadership when required.
Main responsibilities:
Ensure accurate and timely management of pharmacovigilance data including individual case reports, aggregate reports, any PV administrative tasks, local literature monitoring, reconciliation and quality checks.
Assess safety data to identify trends , potential safety observations, and potential signals; notify new safety information to local Health Authority and/or respond promptly to corporate and Health Authority queries.
Ensure local pharmacovigilance activities comply with PSPV policies, global /local PV regulations and all processes and data are always inspection and audit ready.
Support risk management activities and implementation of risk minimization measures in coordination with relevant stakeholders.
Maintain and update PV procedures in line with current regulations and global company policies, supporting training, compliance activities, and corrective and preventative actions.
As designated backup to the Country Safety Head/QPPV, ensure continuity of pharmacovigilance operations and regulatory compliance during absences, including maintaining Health Authority contact relationships and supporting strategic safety leadership when required