Senior CRA
We are seeking a Senior Clinical Research Associate (CRA) to play a key role in establishing and managing our Phase III clinical trial activities in Israel. This is a unique opportunity to take ownership, build infrastructure from the ground up, and grow professionally within an innovative and dynamic organization.
Responsibilities
· Establish the operational infrastructure for a Phase 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