Clinical Research Associate

130 ICR France - FRA

CDI France, France, Paris Santé
Publiée le
23/04/2026
Contrat
CDI · Inconnue
Localisation
France, France, Paris
Taille équipe
Inconnue emp.
Rémunération
Inconnue
Télétravail occasionel 1-3 ans exp. Francais Anglais

Avantages

Horaires de travail flexiblesTickets restaurantMutuelle santéPlan d'épargne pour la retraite collectif (PERCO)Formation en leadership
Missions clés Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials · Ensuring adherence to study protocols, regulatory requirements, and patient safety standards · Building strong relationships with investigators and site staff to support efficient study execution · Reviewing clinical data and resolving queries to maintain accuracy and integrity · Contributing to the preparation and review of key study documents, including protocols and clinical study reports.
Profil recherché Bac +3 (Licence, Bachelor) · 1-3 ans d'expérience · Attention to detail · Organisational skills · Communication skills · Ability to work independently and collaboratively
Outils & compétences Clinical trial processes, International Council for Harmonisation Good Clinical Practice guidelines

Le poste en détail

Site Management I France

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

Join a global leader in clinical research and play a key role in advancing innovative treatments and therapies. As a Clinical Research Associate, you will contribute to the design, monitoring, and analysis of clinical trials, helping to bring new medicines to patients while ensuring the highest standards of quality, safety, and compliance.

Your Responsibilities

In this role, you will take ownership of clinical trial monitoring activities and work closely with cross-functional teams to ensure successful study delivery. Your responsibilities will include:

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
  • Ensuring adherence to study protocols, regulatory requirements, and patient safety standards
  • Building strong relationships with investigators and site staff to support efficient study execution
  • Reviewing clinical data and resolving queries to maintain accuracy and integrity
  • Contributing to the preparation and review of key study documents, including protocols and clinical study reports

Your Profile

You are an experienced and detail-oriented professional with a passion for clinical research and improving patient outcomes. You bring:

  • A bachelor’s degree in a scientific or healthcare-related discipline
  • At least two years of experience working as a Clinical Research Associate
  • Strong knowledge of clinical trial processes, applicable regulations, and International Council for Harmonisation Good Clinical Practice guidelines
  • Excellent organisational and communication skills, with a high level of attention to detail
  • The ability to work both independently and collaboratively in a dynamic environment
  • Flexibility and willingness to travel as required

What We Offer

You will be part of a collaborative and forward-thinking environment where your expertise directly contributes to meaningful scientific progress. This is an opportunity to grow your career while making a tangible impact on the development of life-changing therapies.

If you are ready to take the next step in your clinical research career, we encourage you to apply.

#LI-Hybrid

#LI-VV1

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.

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

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 or submit a request here.

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 click here to apply