לוח משרות דרושים מחקר במדעי החיים בשרון

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.

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.