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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 passionate about making a difference in the lives of people living with Obesity? Do you have a knack for building impactful strategies and fostering meaningful relationships? If so, we invite you to join our company as our new Obesity Consumer Engagement Product Manager. Read on and apply today for a life-changing career!
The position
As an Obesity Consumer Engagement Product Manager at our company, you will play a key role in transforming people living with obesity experience care and support. This is your opportunity to lead meaningful change by putting patients at the heart of everything we do. You will drive new and innovative ways to establish focused strategy to reach out people living with Obesity and Patients already on our innovative obesity treatments. Through cross-functional collaboration and a patient-first mindset, youll be at the forefront of launching impactful initiatives that support both individuals and the healthcare ecosystem.
Your main responsibilities will include:
Leading the launch excellence of anti-Obesity medication, ensuring a smooth and impactful introduction to the market for patients.
Crafting and executing an integrated engagement strategy tailored to the needs of people living with obesity.
Designing strategic communication plans and building meaningful partnerships to increase awareness and impact.
Collaborating with the medical community through scientific dialogue and supporting updates to medical guidelines.
Driving market access efforts, aligning with key stakeholders and payers to ensure broader availability of our treatments.

Are you passionate about ensuring the highest quality standards? Do you have a keen eye for details? We are seeking a Qualified Person (QP) to join our team and help us maintain excellence in our quality management processes. If this sounds like you, read more and apply today for a life-changing career!
The Position
As our Qualified Person you will perform batch release of clinical trial and marketed products in compliance with Ministry of Health (MoH) regulations, in collaboration with Clinical Trials and Commercial Supply Chain teams. You will report directly to Senior QP & PV Manager.
Additionally, you will:
Oversee importation, re-packaging, and quality-related documentation for non-registered products.
Review and maintain quality agreements and SOPs, ensuring alignment with regulatory standards and global procedures.
Investigate and manage deviations, including handling of reports of temperature excursions from pharmacies, hospitals, and distributor premises.
Review Annual Product Reviews (APRs) and support continuous quality improvement activities across the supply chain.

Are you ready to kick-start your career in clinical research with a global healthcare leader? Do you have a passion for ensuring clinical trials run smoothly from the very beginning? Would you like to grow in an innovative environment where your contributions truly matter?
If you answered yes, apply now for the Junior Clinical Start Up Specialist position at our company!
The Position
As our Junior Clinical Start-Up Specialist you will play a vital role in clinical research. You will manage start-up activities for clinical trials, ensuring compliance with local regulations, good clinical practice, our company procedures, and protocol requirements. Your work will focus on delivering reliable data and protecting study participants as you activate trial sites before the first patient visit in the country. Additionally, you will be responsible for executing regulatory submissions, including clinical trial applications, and ensuring timely approvals.
In addition, you will:
Prepare and submit Clinical Trial Applications to Health Authorities and Ethics Committees, ensuring compliance with local regulations, trial protocols, and applicable guidelines
Follow up on submissions until approvals are obtained, and collaborate with teams to answer queries and provide necessary documentation
Maintain effective communication with Health Authorities and Ethics Committees, ensuring all trial team members are informed of submission status and timelines
Manage document translations and approvals, including Clinical Trial product labels and directions for use
Ensure timely updates in the Vault Regulatory Information Management system, maintain confidentiality, and comply with company policies and regulatory requirements.

Are you passionate about driving regulatory strategy, life cycle management of product portfolio and ensuring interactions with regulatory authorities? Do you prosper in a multi-disciplinary environment requiring a unique combination of scientific insights and ability to navigate tight deadlines?
We are looking for an Appointed Pharmacist to join us at our company Israel. Be part of our life-changing careers and apply today!
The Position
As our Appointed Pharmacist, you will be responsible for the oversight of implementing all internal and external regulatory requirements across our portfolio, ensuring our company Israels compliance with the Israeli regulations and the global our companys
Standard Operating Procedures (SOPs). You will report directly to Senior Regulatory Affairs Manager.
Additionally, you will:
Manage and submit regulatory applications (NDAs, variations, labelling updates) to the Israeli Ministry of Health (MoH), ensuring compliance with MoH and our company SOPs.
Review and approve promotional materials, packaging, and safety labelling updates while supporting cross-functional teams in regulatory matters.
Oversee the licensing process for pharmaceutical products in Israel and Palestine, ensuring timely approvals and renewals.
Communicate with MoH and internal stakeholders to ensure compliance, regulatory updates, and approval processes align with business needs.