We're looking for people who have managed complex technology projects, ideally in healthcare or medical devices. Clinical trial experience and experience working inside pharma partnerships are significant advantages.
Major Duties & Responsibilities
Own end-to-end delivery for assigned programs across pipeline, which may span multiple therapeutic areas, stages of development, and partner-sponsored collaborations.
Manage planning, development, testing, and release of digital protocol features required for clinical and commercial readiness.
Build structured delivery plans covering scope, timelines, risks, and dependencies.
Keep Product, Engineering, QA/RA, Clinical, Medical, Regulatory, CMC, and Therapeutics aligned on requirements, timelines, and deliverables.
Serve as \day-to-day delivery counterpart to pharmaceutical partners: manage joint timelines and deliverables, run partner working groups, and prepare materials for joint steering and governance meetings.
Run cross-team meetings that drive accountability and on-time milestones.
Communicate program status, risks, and mitigation plans to internal leadership and external stakeholders.
Coordinate with external partners, including pharmaceutical partners, CROs, clinical sites, and technology vendors, and manage dependencies where partner decisions affect timelines.
Support preparation of program documentation, training materials, and operational tools.
Ensure delivery processes adhere to QMS and relevant regulatory standards for Software as a Medical Device (SaMD) and clinical studies.
Requirements: Bachelor's degree in life sciences, engineering, computer science, or a related discipline. Advanced degree preferred.
3+ years in project or delivery management, preferably within technology, digital health, medical devices, or SaMD.
Track record managing complex cross-functional projects from planning through delivery.
Clinical trial experience (Phase 1 to 3), or direct collaboration with CROs or clinical sites, is a strong advantage.
Experience delivering projects within a pharma or biotech partnership, alliance, or co-development structure is a strong advantage.
Strong understanding of the software development lifecycle, agile methodologies, and release management.
Excellent stakeholder management across technical, clinical, and operational teams.
Comfortable representing the company to senior external stakeholders and managing timelines you don't fully control.
Able to manage multiple priorities and deliver in a fast-paced environment.
Highly organized, detail-oriented, and a proactive problem solver.
Excellent written and verbal communication in English and Hebrew.
This position is open to all candidates.