Sponsor Dedicated Clinical Trial Manager - Home based EMEA, Hebrew Speaker

Overview

Sponsor Dedicated Clinical Trial Manager - Home based EMEA, Hebrew Speaker

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model puts the customer and the patient at the center of everything we do.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with problem solvers to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies.

Discover what our 29,000 employees, across 110 countries already know: WORK HERE MATTERS EVERYWHERE.

Job Responsibilities

Fluency in Hebrew and deep knowledge of Israeli clinical processes are essential requirements.

The role will be accountable for overseeing and maintaining country (Israel) deliverables as part of the overall project plan. Manages and maintains accurate country level plans. Ensures timely bidirectional communication between the global and local study team. Cluster-focused stakeholder management.

Main Responsibilities

• Responsible for documented review for reports/issues written by the CRAs/Lead CRAs.
• Drives recruitment at regional/country level.
• Responsible for local country vendor management and oversight (as applicable).
• Drives data cleaning at regional/country level.

Requirements

• Hebrew fluency
• Previous experience with Israeli sites and knowledge of Israeli RA contacts and regulatory and submissions processes

• Background & Expertise:
• Preferably with historical CRA or strong site-level experience
• Solid understanding of site operations and dynamics.

• Start-Up Phase Experience:
• Involvement in site selection, feasibility assessments, timeline planning, and recruitment support.
• Experience working with vendors during study setup.

• Conduct Phase Responsibilities:
• Ability to support the study team during audits, inspections, and query resolution.
• Strong leadership skills to manage complex or challenging conversations.
• Experience in Oncology field and across different study phases

• Local Knowledge & Language:
• Deep understanding of local (Israeli) regulatory and ethics processes.
• Fluency in Hebrew

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health at

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will be considered. The Company will determine what constitutes equivalent qualifications. This description does not create an employment contract. The language herein is intended to comply with the laws of each country in which it operates, including the EU Equality Directive. The Company is committed to compliance with the Americans with Disabilities Act, including reasonable accommodations when appropriate.

Summary

Roles within the Clinical Trial Management job family at the P22 level are responsible for overseeing the development, coordination, and implementation of Phase 1 clinical research studies. These roles collaborate with the principal investigator, coordinate with client teams and operations, and track study progress against milestones, deliverables, and budget while ensuring regulatory compliance globally and regionally. They contribute to the design, implementation, and delivery of processes, programs, and policies, and may manage work of lower-level professionals to ensure efficient and effective clinical trials.