Study Start Up Clinical Research Associate

About the role

IQVIA is seeking a motivated Study Start‑Up Clinical Research Associate to join its sponsor‑dedicated team. In this role you will support site preparation, identify early site needs, and ensure a smooth hand‑over to execution teams.

Key responsibilities

• Perform site selection and verify eligibility for studies across phases I‑IV.
• Serve as the primary contact for trial sites during selection, start‑up, and IRB/IEC and health authority submission preparation.
• Collect site‑specific submission documents (e.g., FDA forms, CVs, GCP certificates, DSL) within agreed timelines.
• Collaborate with start‑up team members to meet country‑specific timelines and deliverables.
• Evaluate site practices against regulatory requirements, Good Clinical Practice and ICH guidelines.
• Track progress of regulatory submissions, recruitment, case report form completion, and data query resolution.
• Work closely with site experts and client representatives to address issues and manage risk.

Required profile

• University degree in a scientific discipline or health‑care field.
• Experience in submissions, site identification, issue management and risk identification.
• Excellent command of Hebrew and English.
• Strong organizational, time‑management and problem‑solving abilities.
• Ability to build effective relationships with coworkers, managers and clients.
• Willingness to travel as needed.

Required skills

• Proficient use of MS Office applications.