Project Manager
The Project Manager is responsible for leading the execution, coordination, and delivery of Remepy’s Parkinson’s disease (PD) Phase 3 hybrid trial. This role focuses on ensuring the complete readiness of the product and related operational processes necessary for a successful clinical trial launch. The role requires strong coordination across internal teams and external partners, including the CRO and clinical sites. Experience managing complex technology projects- ideally in healthcare or medical devices; clinical trial experience is a significant advantage.
Location
Ramat Gan (Bursa), Israel
Reports to
Director of Project Management
Company Overview
Remepy is a digital health company specializing in the development of hybrid drugs – a product that includes a traditional pharmacological component and a digital therapeutic app. Remepy’s digital therapeutics applications are developed as Software as a Medical Device (SaMD), in accordance with applicable medical device regulations of the US Food and Drug Administration (FDA) and the International Organization of Standards (ISO). The company is headquartered in the US with R&D operations in Ramat Gan, Israel. As the legal manufacturer, Remepy is responsible for management oversight, regulatory affairs, quality system compliance, document control, design and development, procurement, marketing and sales, complaint handling, manufacturing, and distribution or deployment of its products.
Major Duties & Responsibilities
- Manage planning, development, testing, and release of app features necessary for clinical trial.
- Ensure alignment across Product, Engineering, QA/RA, Clinical, and Therapeutics teams on requirements, timelines, and deliverables.
- Develop a structured delivery plan that includes scope, timelines, risks, and dependencies.
- Facilitate cross-team meetings to ensure accountability and timely completion of all milestones.
- Communicate program status, risks, and mitigation strategies to internal leadership and external stakeholders.
- Coordinate with Clinical Operations to ensure Remepy’s complete readiness for Phase 3.
- Serve as the primary liaison between Remepy, CRO partners, and clinical sites.
- Support preparation of trial documentation, training materials, and operational tools.
- Ensure all delivery processes adhere to Remepy’s QMS and relevant regulatory standards for SaMD and clinical studies.
Preferred Qualifications
- Bachelor’s degree in life sciences, engineering, computer science, or related discipline; advanced degree preferred.
- 3+ years of experience in project or delivery management, preferably within technology, digital health, medical devices, or SaMD.
- Demonstrated experience managing complex cross-functional projects from planning through delivery.
- Clinical trial experience (Phase 1–3) or direct collaboration with CROs or clinical sites is a strong advantage.
- Strong understanding of software development lifecycle, agile methodologies, and release management.
- Excellent communication and stakeholder management skills across technical, clinical, and operational teams.
- Proven ability to manage multiple priorities and deliver results in a fast-paced environment.
- Highly organized, detail-oriented, and proactive problem solver.
- Excellent communication skills, both written and verbal, in English and Hebrew.