About Remepy

Remepy is pioneering a new category of therapy by combining pharmaceuticals with targeted digital interventions. Our mission is to deliver more personalized, adaptive, and effective care - helping patients heal through the unified power of biology, behavior, and technology. We’re a team of scientists, technologists, clinicians, and creators driven by one belief: the future of medicine is multidimensional.

Responsibilities

· Establish the operational infrastructure for a Pha se III clinical trial in Israel

· Lead and manage submissions to IRBs (Helsinki Committees)

· Initiate clinical sites and oversee site activation processes

· Perform monitoring and provide ongoing management and support to trial sites in Israel

· Arrange and coordinate all local logistics related to the clinical trial

· Support the VP of Clinical Operations with study documentation, study setup, and global-level clinical trial activities

Qualifications

· Bachelor’s degree or higher in Life Sciences or a paramedical profession (e.g., nursing, pharmacy, clinical dietetics, etc.)

· Minimum of 2-3 years of experience in clinical research within pharmaceutical, medical device, or CRO environments

· Strong understanding of site-level clinical trial management, including monitoring, investigational product handling, and regulatory binder management

· In-depth knowledge of Israeli clinical trial regulations and ICH-GCP guidelines

· Proven experience managing site submissions and site-level regulatory documentation

· Willingness to travel to clinical trial sites across Israel

· GCP certification

· CRA certification- advantage

· Experience with Phase III trials – advantage

· Knowledge or experience in Parkinson’s disease – advantage

· Experience working in a startup environment – advantage

• · Native or high-level English proficiency with excellent written and verbal communication skills