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

Overview

Sponsor Dedicated Clinical Trial Manager - Home based EMEA, Hebrew Speaker. Updated:
February 20, 2026.

Location:

Amsterdam, NH, Netherlands. Job :

-OTHLOC-3528-2DR.

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model places the customer and the patient at the center of everything we do, with a focus on simplifying and streamlining work to better serve our customers and patients.

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

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

Why Syneos Health

• We are passionate about developing our people through career development, progression, training, and rewards.
• We maintain a Total Self culture that encourages authenticity and care for our people.
• We value diversity of thoughts, backgrounds, cultures and perspectives to ensure everyone feels they belong.

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

• Oversee and maintain country (Israel) deliverables as part of the overall project plan; manage and maintain accurate country-level plans.
• Ensure timely bidirectional communication between the global and local study teams; engage in cluster-focused stakeholder management.
• Documented review of reports/issues written by the CRAs/Lead CRAs.
• Drive recruitment at regional/country level.
• Oversee local country vendor management as applicable.
• Drive data cleaning at regional/country level.

• Hebrew fluency
• Previous experience with Israeli sites and knowledge of Israeli RA contacts and regulatory and submissions processes
• At least 3 years of experience as a Clinical Trial Manager

• 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 with vendors during study setup.
• Conduct Phase Responsibilities
  :
  Ability to support the study team during audits, inspections, and query resolution; strong leadership for complex conversations; experience in Oncology and across study phases preferred.
• Local Knowledge & Language
  :
  Deep understanding of local Israeli regulatory and ethics processes;
  Hebrew fluency.

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 your role, you’ll take initiative and challenge the status quo in a dynamic environment. Learn more about Syneos Health at

Tasks, duties, and responsibilities as listed are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks. Equivalent experience, skills, and/or education will be considered. The Company will determine what constitutes equivalent qualifications. Nothing herein should be construed as an employment contract. Language is intended to comply with country legislation, including the EU Equality Directive, in relation to recruitment and employment.

The Company is committed to compliance with the Americans with Disabilities Act, including reasonable accommodations when appropriate.

Roles within the Clinical Trial Management job family at the M24 level serve as the clinical functional lead for site management, clinical monitoring and central monitoring of assigned study(ies). The position provides leadership, problem-solving, mentoring, and technical support to the Clinical Operations team to ensure compliance with the monitoring plan and timely, quality deliverables within budget. The Senior CTM may provide direction and coordination across regions and/or countries to ensure clinical project and site deliverables are met.