Excelya

Clinical Operations Lead

🇫🇷 Lyon, França Híbrido Saúde e ciência Tempo inteiro Lead Publicado Mai 26, 2026
Localização Lyon, França
Modalidade Híbrido
Contrato Tempo inteiro
Senioridade Lead
Categoria Saúde e ciência
Idioma English
Publicado 26 de Maio de 2026
Última verificação 27 de Maio de 2026
Contexto da JobGrid

Resumo da vaga pela JobGrid

Clinical Operations Lead at Excelya: Lyon, França; Híbrido; Tempo inteiro; Lead; Saúde e ciência. JobGrid adds normalized role facts, source context, and a path to the employer application page so candidates can compare the listing before applying.

  • Location and workplace: Lyon, França, Híbrido
  • Role classification: Saúde e ciência, Tempo inteiro, Lead
  • Source freshness: checked by JobGrid on 2026-05-27.
  • Application path: candidates continue to the employer application page with non-personal referral tags.

About the Job

At Excelya, we are committed to fostering an environment defined by Audacity, Care, and Energy. As a Clinical Operations Lead , you will play a vital role in enhancing our clinical research strategies and ensuring operational excellence across our studies.

This position offers a unique opportunity to lead a dedicated team while collaborating with various stakeholders to uphold the highest standards of quality in clinical operations. You will be instrumental in driving innovation and contributing to cutting-edge research initiatives that shape the future of healthcare.

Main Responsibilities

  • Overall leadership of clinical projects and cross-functional team coordination, including identification, onboarding, and management of clinical sub-teams, as well as facilitation of project and team meetings with internal and external stakeholders (including CROs)
  • Strong oversight of CRO partners: coordination of activities, performance monitoring, alignment with clinical strategy, risk and escalation management, and ensuring high-quality deliverables
  • Contribution to the development and execution of clinical operational strategies (TPP, CDP, etc.), ensuring alignment with project objectives and driving innovative and efficient approaches
  • Ownership of timeline management through planning tools (RDPM), including setup, monthly updates, simulation scenarios, and adherence to key milestones
  • Rigorous budget management: tracking, updating, and reviewing costs (eCote, RDPM, CASA), ensuring alignment with strategic and operational plans
  • Structured and timely reporting of project activities (clinical supply planning, time tracking, progress updates, risks) to management and stakeholders
  • Driving team engagement and fostering a collaborative environment, ensuring strong communication, alignment, and team performance
  • Contribution to broader platform activities, including process improvement initiatives, participation in working groups, acting as a subject matter expert, and delivering training sessions