לוח משרות דרושים רפואה ופארמה בשרון

Are you ready to make a difference in the world of healthcare? At AstraZeneca, 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 AstraZeneca's 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 AstraZeneca 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.

Are you ready to lead a groundbreaking initiative that bridges local capabilities with global needs? As the Head of Beam and Evidence Generation Lead, you will spearhead global Real-World Data Research Center (Beam) in Israel, while guiding evidence generation activities across all therapeutic areas. This dual role leverages Israel's unique healthcare data infrastructure to generate real-world insights that advance patient care both locally and globally. Your leadership will be pivotal in establishing strategic partnerships with academic institutions, healthcare organizations, and technology companies, ensuring research activities meet the highest scientific, ethical, and regulatory standards. Are you prepared to transform complex healthcare data into meaningful insights that drive innovation and improve patient outcomes?

Accountabilities:
Lead the strategic and scientific direction, operational management, and growth of Beam, ensuring alignment with global priorities.
Foster strategic partnerships with healthcare organizations and tech companies to advance healthcare innovations globally.
Manage a team of data scientists and epidemiologists to address global data needs.
Cultivate scientific collaborations across internal and external teams, building trusted relationships with researchers and stakeholders.
Oversee budget management and resource allocation to ensure operational efficiency.
Represent Beam at scientific conferences, industry forums, and strategic partnership discussions.
Accountable for strategical guidance, planning, development, and operational delivery of local studies across all therapeutic areas.
Lead the development of multi-annual evidence generation plans aligned to business strategy.
Foster collaborations with external experts to conduct high-impact RWE studies.
Implement global governance frameworks to ensure compliance with legislation, SOPs, and GCP.
Ensure effective communication of study results at congresses and publication in journals.
Support Business Units in identifying evidence solutions that address business needs.

Join our dedicated Clinical Research team as a Clinical Research Associate (CRA). In this role, you will have local responsibility for the delivery of studies at allocated sites and will be an active participant in the local study team(s). You will work in close collaboration with other CRAs and the Local Study Team/ Local Study Manager to ensure that study commitments are achieved in a timely and efficient manner. This is your chance to strengthen our pipeline and make a meaningful impact on patients' lives!

Accountabilities:
As a CRA, you will contribute to the selection of potential investigators, train, support and advise Investigators and site staff in study-related matters, and ensure that study sites are inspection ready at all times. You will also be responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, ensuring compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant 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