Study Start Up Clinical Research Associate

IQVIA is looking for talented and motivated team member to join our Sponsor dedicated team as Study Start Up Clinical Research Associate. At this position you would be responsible of site preparation and early identification of real site needs and issues and close handover to execution CRA

Your responsibilities will include:

• Performing site selection verification of the elegibility for studies from phase I-IV.
• Acts as the main contact for trial sites during site selection, study start-up and IRB/IEC and HA submission preparation.
• Collects submission-related site-specific documents for all relevant site personnel within agreed timelines (e.g., FD, CV, GCP certificates, DSL, etc.)
• Collaborates with the other team members of start up in timelines and deliverables are met according to country commitments.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
• Collaborating with experts at study sites and with client representative
  
  

• University degree in scientific discipline or health care
• Experience in Submissions, Site Identification, issue management and risk identification.
• Very good computer skills including MS Office
• Excellent command of Hebrew and English language.
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Flexibility to travel