CTM

Pharmaceutical Research Associates, Inc; France; Hybride; EUR 45 000 - 65 000; Plein temps

Résumé du poste

Une entreprise de recherche clinique de premier plan recherche des Clinical Trial Managers pour rejoindre son équipe dédiée à Paris/Ile-de-France. Le candidat idéal aura une expérience dans la gestion d'essais cliniques, avec des responsabilités allant de la planification à la mise en œuvre des études cliniques. ICON offre un environnement de travail hybride avec des avantages axés sur le bien-être et l'équilibre travail-vie personnelle.

Prestations

Assurance santé

Planification de la retraite

Programme d'assistance aux employés

Assurance vie

Congés annuels

Avantages optionnels (bons de garde d'enfants, réductions de gym, etc.)

Qualifications

• Expérience en tant que CTM ou Local Trial Manager dans l'industrie pharmaceutique ou CRO.
• Compétences en monitoring.
• Fluency in French and professional proficiency in English.

Responsabilités

• Planifier et gérer l'exécution des études cliniques.
• Être responsable des livrables d'étude en France.
• Collaborer avec les équipes locales pour assurer l'alignement avec les attentes mondiales.

Connaissances

Organizational skills

Communication skills

IT skills

Multitasking

Adaptability

Description du poste

Overview

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations.

With our patients at the center of all we do, we help accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures excellence in our work.

Responsibilities

We are constantly looking for motivated, reliable, and dedicated CTMs in the Paris/Ile-de-France area to join our sponsor-dedicated team!

You will have similar experience as a Clinical Trial Manager, Local Trial Manager, or Study Manager within the pharmaceutical industry or a CRO.

The role requires 1-3 days/week at the client office.

You will be the primary contact responsible for leading, managing, and coordinating the conduct of clinical trials from start-up to close-out at a country level in France. You will ensure the quality and scientific integrity of the trials. The Local Trial Manager collaborates with cross-functional stakeholders to ensure timely and budget-conscious execution of clinical trial deliverables within the country.

Key responsibilities include:

• Planning, managing, and overseeing clinical study execution in line with the global program strategy
• Being accountable for study deliverables in France
• Leading country-level operational planning and supporting site selection
• Keeping key stakeholders informed of study progress
• Communicating country status, including timelines and deliverables, to stakeholders and updating relevant systems
• Overseeing vendor activities such as laboratories and equipment provisioning
• Monitoring the execution of the clinical study against timelines, deliverables, and budget
• Reviewing Monitoring Visit Reports
• Contributing to study-level forecasting, accountability, reconciliation, and ELE process management
• Executing regulatory inspection readiness activities
• Assigning and overseeing study support staff deliverables
• Collaborating with local teams to ensure alignment with global expectations

Qualifications

Requirements:

• Experience as a CTM, Local Trial Manager within the pharmaceutical industry or CRO
• Monitoring experience
• Excellent organizational skills
• Ability to adapt and prioritize in a dynamic environment
• Strong IT skills
• Effective communication skills, capable of multitasking and working under pressure
• Fluency in French and professional proficiency in English

What ICON offers: Our success depends on our people. We prioritize building a diverse culture that rewards high performance and nurtures talent. Along with a competitive salary, ICON provides various benefits focused on well-being and work-life balance, including:

• Annual leave entitlements
• Health insurance options
• Retirement planning
• Global Employee Assistance Program (TELUS Health)
• Life assurance
• Optional benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, health assessments, etc.

#LI-DC1#LI-Hybrid

Visit our careers website to learn more about working at ICON: https://careers.iconplc.com/benefits

ICON, including subsidiaries, is an equal opportunity employer committed to a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. If you need a reasonable accommodation during the application process or to perform essential job functions, please let us know or submit a request here.

Interested but unsure if you meet all requirements? We encourage you to apply—there’s a good chance you are exactly what we’re looking for, whether for this or other roles at ICON.