Clinical Trial Manager

ICON Strategic Solutions; France; Sur place; EUR 40 000 - 60 000; Plein temps

Résumé du poste

A leading healthcare intelligence firm in France is seeking a Regulatory Submission Lead to manage clinical trials and oversee submissions. The ideal candidate will hold a university degree in medicine or science, possess strong knowledge of clinical systems, and be proficient in both French and English. This role involves collaboration with cross-functional teams and ensuring compliance with regulatory standards.

Prestations

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Employee Assistance Programme

Flexible optional benefits

Qualifications

• University degree in medicine, science, or equivalent.
• Demonstrated ability to drive the clinical deliverables of a study.
• Subject matter expertise in designated therapeutic area.

Responsabilités

• Plan and manage all aspects of clinical trials.
• Oversee clinical trial submissions and approvals.
• Collaborate with cross-functional teams.

Connaissances

Strong knowledge of core clinical systems

Excellence in French

Problem-solving skills

Ability to drive clinical deliverables

Knowledge of local regulatory processes

Formation

University degree in medicine or science

Description du poste

Overview

Regulatory Submission Lead

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

What you will be doing

• Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards.
• Oversee clinical trial submissions and approvals at the country level, including preparation of local language materials and coordination with Ethics Committees and Regulatory Authorities.
• Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
• Build and manage strong relationships with trial investigators and stakeholders.
• Ensure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
• Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.

Your Profile

• University degree in medicine, science, or equivalent combination of education & experience
• Strong knowledge of core clinical systems, operational tools, and performance metrics.
• Solid understanding of local regulatory processes for clinical trial submissions and approvals.
• Excellent proficiency in French and English.
• Demonstrated ability to drive the clinical deliverables of a study
• Subject matter expertise in the designated therapeutic area
• Prior monitoring experience is preferred
• Ability to travel up to 20%

What ICON can offer you

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

Equity, inclusion and non-discrimination

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee? Please apply here.