Senior Cra

Senior CRA (Late Phase), France, Paris, Remote,

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

ICON Commercialisation & Outcomes (ICO) optimises the value of drugs and medical devices through innovative strategies that reflect evolving evidentiary, regulatory, and reimbursement requirements. Our expert team communicates a product’s unique clinical and economic value, enabling success in today’s dynamic and patient-centric healthcare environment.

ICO helps clients make evidence-based, commercially sound decisions early in development—supporting the introduction of high-value products to the market in the shortest time possible.

As a Senior Clinical Research Associate (Senior CRA) within ICO’s late-phase research group, you will be instrumental in executing and driving site and patient engagement activities across a variety of post-marketing and real-world evidence studies. Working within a hybrid model that supports project management and cross-functional collaboration, you’ll play a vital role in ensuring that our clients’ studies are delivered on time, within scope, and with the highest quality.

This role offers an excellent opportunity to contribute not only as a senior-level monitor but also as a key partner in building and refining operational processes within a fast-evolving group.

What You Will Be Doing:

- Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
- Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

- Advanced degree in a relevant field such as life sciences, nursing, or medicine.
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
- Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.

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.

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