Clinical Trial Manager — Sponsor Dedicated (Hybrid, Paris)

Syneos Health, Inc.; Montrouge; Hybride; EUR 80 000 - 120 000; Plein temps

Avantages offerts par ce poste

Competitive remuneration package

Career development and training

Opportunity to progress career

Résumé du poste

Syneos Health is seeking a Clinical Trial Manager for sponsor-dedicated work in a hybrid setup. The role covers country-level oversight from startup to closeout, with 50% time based at client offices in Paris and 50% remote.

You will coordinate cross-functional teams, manage timelines and budgets, and ensure data integrity across CTMS/eDC systems. The ideal candidate has GCP/ICH expertise, strong regulatory knowledge, and proven leadership in clinical research projects.

Qualifications

• GCP and ICH guidelines knowledge is essential for compliance.
• Strong understanding of clinical research processes and regulations.
• Experience leading cross functional teams and managing priorities.

Responsabilités

• Provide country-level oversight from startup to closeout with time, budget and quality accountability.
• Serve as main contact for internal/external stakeholders at country level.
• Coordinate cross-functional teams and site feasibility with country study targets.
• Lead risk assessment, issue resolution, and CAPA where needed.
• Ensure data in CTMS/eDC systems is current and accessible to the country team.
• Prepare country-specific documents and support Health Authority submissions.

Connaissances

GCP & ICH

Regulatory knowledge

Clinical research

Cross-functional leadership

Organization & planning

Risk analysis

Communication skills

Tech proficient

Formation

Bachelor's degree in life sciences

Clinical research certification

Outils

CTMS

eTMF

eDC access

Description du poste

Syneos Health is seeking a Clinical Trial Manager for sponsor-dedicated work in a hybrid setup. The role covers country-level oversight from startup to closeout, with 50% time based at client offices in Paris and 50% remote.

You will coordinate cross-functional teams, manage timelines and budgets, and ensure data integrity across CTMS/eDC systems. The ideal candidate has GCP/ICH expertise, strong regulatory knowledge, and proven leadership in clinical research projects.