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Join Us as a Clinical Trial Coordinator - Make an Impact at the Forefront of Innovation
As part of our global team, youll have the opportunity to provide administrative and technical support to the Project Team. As a Clinical Trial Coordinator, you'll coordinate and facilitate project activities and may serve as a study lead, acting as a cross-functional liaison for the project team. You will act as a buddy during the onboarding phase and provide training to new staff as needed. Additionally, you will support departmental and cross-functional initiatives for process improvements and enhancements.
What Youll Do:
According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix.
Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in appropriate system.
Ensures allocated tasks are performed on time, within budget and to a high quality standard. Proactively communicates any risks to project leads and line manager as appropriate.
Supports the maintenance of study specific documentation and global support with specific systems, tools and trackers including but not limited to: study team lists, tracking of project specific training requirements, system access management for organization/vendor/clients, and tracking of project level activity plans in appropriate system. Ensures (e)TMF is up to date by following file review schedules and documents findings in appropriate system.
Provides system support (i.e. GoBalto & eTMF).
Supports RBM activities.
Performs administrative tasks on assigned trials including but not limited to: timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, performing mass mailings and communications as needed, providing documents and reports to internal team members.
Supports scheduling and organization of client and/or internal meetings with completion of related meeting minutes.
Reviews and tracks local regulatory documents.
Transmits documents to client and centralized IRB/IEC.
Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
Maintains vendor trackers.

We are looking for a Senior AI Researcher to work closely with our delivery team, translating real-world clinical and scientific questions into rigorous AI and machine learning solutions. In this role, you will lead the development of methodologies, models, and benchmarking frameworks that address complex clinical problems using our unique immune-cell data. Your work will directly impact how our partners understand biology, evaluate hypotheses, and make decisions.

Location: Ramat Gan (hybrid model).

What will you do?
Partner with the collaborations team and scientists to frame complex clinical and biological questions as well-defined data science and modeling problems.
Design, implement, and evaluate the right analytical and modeling approaches for each problem, including robust benchmarking and validation strategies.
Clearly communicate results, limitations, and tradeoffs to internal teams and external partners, enabling confident, data-driven decisions.
Establish best practices for rigor, reproducibility, evaluation, and documentation across delivery-focused data science work.
Work hand-in-hand with immunologists, computational biologists, AI scientists, and engineers to ensure solutions are scientifically sound and production-aware.
Translate modeling solutions into engineered and iterable products used by the internal collaborations team.