In this role, you will manage a team of talented CRAs working across a diverse portfolio of innovative medical device trials. You will have the opportunity to drive study execution, mentor team members, and collaborate with leading medical device companies across global markets.
Responsibilities:
Oversee day-to-day clinical trial operations from planning to close-out.
Directly manage a team of CRAs working on multiple clinical projects.
Provide ongoing training, support, and professional development to CRAs.
Ensure all studies are conducted in compliance with GCP, ISO 14155, and local
regulatory requirements.
Collaborate with sponsors, clinical sites, and cross-functional teams to ensure quality
and timelines are met.
Contribute to SOPs development, internal quality initiatives, and resource planning.
Requirements: At least 5 years of hands-on experience managing clinical trials, with a strong focus on
medical devices.
Previous experience in line management or direct supervision of clinical staff must.
Proven understanding of GCP, ISO 14155, and regulatory frameworks for medical
devices.
Excellent communication and interpersonal skills were looking for a warm,
professional team player who can mentor others and lead with empathy.
Fluent in English (written and spoken); Hebrew an advantage.
Industry
Professional Services
Employment Type
Full-time
This position is open to all candidates.
