Description
Syneos Health is seeking an experienced Clinical Research Associate to work within the team of a global Pharma client. The role is permanent and fully dedicated to one sponsor.
As a Clinical Research Associate, you will be responsible for the full range of activities from study set-up through to close-out.
Responsibilities:
- Assess potential investigators and decide on the suitability of the site.
- Develop/adapt recruitment and retention strategy for the site.
- Ensure that the current versions of the trial documents that are listed on the Site Initiation Report and all required trial-related materials and supplies are provided to the investigational site.
- Negotiate investigator budgets at site level and track the status of site CTA.
- Plan and conduct investigator and site-staff training.
- Conduct site initiation, monitoring and closure visits.
- Create site specific and monitoring tools.
- At the investigational site, ensure clinical drug supplies are available, appropriately used, handled, stored (e.g., temperature logs, security), and returned, accurately inventoried and documented.
Qualifications:
- 2 years + of hands-on Monitoring experience with Israeli sites and with pharmaceutical drugs clinical trials
- Experience with Oncology/Hemato-Oncology studies is an advantage
- Experience with RBM would be highly preferred
- Fluent in Hebrew as well as a good level of English
- Ready to frequent business trips (75% of time)
- Strong communication and interpersonal skills, a motivation towards strong teamwork and enjoy building relationships