CTM

ICON Strategic Solutions; France; Hybride; EUR 50 000 - 70 000; Plein temps

Résumé du poste

ICON Strategic Solutions is seeking a Clinical Trial Manager in the Paris/Ile-de-France area to oversee clinical trials. The role involves managing study execution, ensuring compliance with regulations, and collaborating with stakeholders. Ideal candidates will have experience in the pharmaceutical industry and strong organizational skills.

Prestations

Various annual leave entitlements

Health insurance options

Retirement planning options

Global Employee Assistance Programme

Life assurance

Flexible country-specific benefits

Qualifications

• Stable experience as a CTM or Local Trial Manager in the pharmaceutical industry or CRO.
• Prior monitoring experience.
• Fluency in French and professional proficiency in English.

Responsabilités

• Lead, manage, and coordinate clinical trials from start-up to close-out.
• Ensure timely and on-budget execution of clinical trial deliverables.
• Oversight of vendor activities and monitoring study execution.

Connaissances

Organization

Communication

IT Skills

Multitasking

Description du poste

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

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

Our people are our greatest strength, are 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 what we do, we do well.

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 demonstrate some similar experience as a Clinical Trial Manager, Local Trial Manager, or Study Manager within the pharmaceutical industry or a CRO.

The format will be 1-3 days/week at the client office.

In this role, you will be a primary point of contact to lead, manage, and coordinate the conduct of clinical trials from study start-up to close-out at a country level in France. You will maintain the quality and scientific integrity of clinical trials at a country level. The Local Trial Manager collaborates with cross-functional stakeholders to ensure timely and on-budget execution of clinical trial deliverables within the country.

Key responsibilities include:

• Planning, management, and oversight of clinical study execution in accordance with the global program strategy
• Accountable for study deliverables in France
• Leading country-level operational planning and supporting site selection within the assigned country
• Ensuring key stakeholders are kept informed of study progress
• Communicating country status (including timelines and deliverables) to key stakeholders and ensuring updates to relevant systems
• Oversight and monitoring of applicable vendor activities, e.g., laboratories and equipment provisioning
• Monitoring the execution of the clinical study against timelines, deliverables, and budget for France
• Reviewing Monitoring Visit Reports
• Contributing to the study-level forecast for investigational product, supporting study-level accountability and reconciliation, management of ELE process
• Executing regulatory agency inspection readiness activities
• Assigning and overseeing deliverables of study support staff
• Collaborating with local teams to ensure country-level study delivery aligns with global expectations

You will need:

• Some stable experience as a CTM, Local Trial Manager within the pharmaceutical industry or CRO
• Prior monitoring experience
• Excellent organization skills
• Ability to work well in a dynamic environment and prioritize/respond to changing needs
• Strong IT skills
• Strong communication skills with the ability to multitask and work effectively under pressure
• Fluency in French and professional proficiency in English

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve prioritized building a diverse culture that rewards high performance and nurtures talent.

In addition to a competitive salary, ICON offers a range of benefits focused on well-being and work-life balance, including:

• Various annual leave entitlements
• A range of health insurance options
• Retirement planning options
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to support professionals
• Life assurance
• Flexible country-specific benefits such as childcare vouchers, bike schemes, gym discounts, travel passes, health assessments, and more

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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 the essential functions of a role, please let us know or submit a request here.

We encourage you to apply even if you’re unsure if you meet all the requirements — you might be exactly what we’re looking for.