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

Overview

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 brings the customer and the patient to the center of everything that we do. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals.

WORK HERE MATTERS EVERYWHERE

Responsibilities

• Oversee and maintain country (Israel) deliverables as part of the overall project plan; manage and maintain accurate country level plans.
• Ensure timely communication bidirectionally between the global and local study team;
  - focused stakeholder management.
• Responsible for documented review of reports/issues written by the CRAs/Lead CRAs.
• Drives recruitment at regional/country level.
• Responsible for local country vendor management and oversight (as applicable).
• Drive data cleaning at regional/country level.

Qualifications

• Fluency in Hebrew; deep knowledge of Israeli clinical processes are essential 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
  - 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 conversations; experience in Oncology and across different study phases.
• Local Knowledge & Language: deep understanding of local (Israeli) regulatory and ethics processes.

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
- changing environment. Learn more about Syneos Health at http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. The Company may consider equivalent experience, skills, and/or education in lieu of listed qualifications. The Company will determine what constitutes equivalent qualifications. Nothing herein should be construed to create an employment contract. All statements are intended to comply with applicable law in each country of operation, 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, serve as liaisons between research subjects, client teams, investigators, and clinic operations teams, and meticulously plan logistics and resource usage. They track study progress in alignment with project milestones, client deliverables, and budget, while ensuring regulatory compliance globally and by region.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Research, Analyst, and Information Technology

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