JUMP TO CONTENT

CRA I

  1. Paris
JR154532
  1. Clinical Monitoring
  2. ICON Full Service & Corporate Support
  3. Hybrid

About the role

This vacancy has now expired. Please click here to view live vacancies.

CRA I, Sponsor Dedicated, Paris, Hybrid.

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.

Clinical Research Associate I (CRA I) — Sponsor-dedicated, Paris

As a CRA I at ICON, you will join a team dedicated to a single global pharmaceutical sponsor, based in Paris. Working across Phase I to III trials in neurology, dermatology, oncology and rare diseases, you will contribute to our clinical trial operations function and help deliver high-quality outcomes across the sponsor's programmes.

What you will do

  • Your role centres on delivering clinical trial monitoring to a high standard, working closely with your team, the sponsor and study sites. Key responsibilities include:
  • Coordinating the set-up and monitoring of studies independently, producing accurate study status reports and maintaining study documentation.
  • Resolving sponsor-generated queries efficiently and supporting study cost-efficiency, including contributing to the preparation and review of study documentation and feasibility assessments for new proposals.
  • Building and maintaining strong, collaborative relationships with key stakeholders, clinical investigators and site staff.
  • Safeguarding patient safety by ensuring compliance with ICON's procedures, protocols and regulatory requirements.

Your profile

  • You will bring relevant clinical trial monitoring experience (6-12 months within a CRO) along with:
  • A university degree in medicine, life sciences, pharmacy or a related field.
  • Working knowledge of ICH-GCP guidelines and the ability to review and evaluate medical data.
  • Fluent French and English, written and spoken.
  • Strong interpersonal skills, enabling you to handle queries promptly and professionally.
  • Willingness to travel 8 times per month.

Why this role

Dedicated to a single sponsor, you will get to know their pipeline in depth and build lasting relationships with their teams, with the training, stability and long-term career progression of one of the world's largest CROs behind you.

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.

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

List #1

Day in the life

A picture of Suzaita
Suzaita's story - an insight into working in Clinical Research

Teaser label

A Day In The Life

Content type

Blogs

Publish date

04/05/2023

Summary

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil

Teaser label

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Read more
Suzaita Hipolito

by

Suzaita Hipolito

Suzaita Hipolito

by

Suzaita Hipolito

View all

Similar jobs at ICON

Senior CRA- Phase I Oncology-NY/NJ

Salary

Location

US, Farmingdale, NY

Location

New York

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR156413

Expiry date

01/01/0001

Melissa Benner Read more Shortlist Save this role
Senior CRA- Phase I Oncology- NY/NJ/PA

Salary

Location

US, New York, NY, Rochester

Location

Boston

Rochester

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR156415

Expiry date

01/01/0001

Melissa Benner Read more Shortlist Save this role
Senior CRA- Phase I Oncology- NY/NJ/PA

Salary

Location

US, New York, NY, Rochester

Location

Boston

Rochester

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR156417

Expiry date

01/01/0001

Melissa Benner Read more Shortlist Save this role
Senior CRA- Phase I Oncology- IA/CO/UT/NE

Salary

Location

US, McFarland, IA

Location

McFarland

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR156410

Expiry date

01/01/0001

Melissa Benner Read more Shortlist Save this role
Senior CRA- Phase I Oncology- NJ/NY

Salary

Location

US, New York, NY, Rochester

Location

Boston

Rochester

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR156412

Expiry date

01/01/0001

Melissa Benner Read more Shortlist Save this role
Senior CRA

Salary

Location

US, Bristol, TN

Location

Boston

Bristol

Remote Working

Remote

Business Area

ICON Strategic Solutions (FSP)

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:

Reference

JR156396

Expiry date

01/01/0001

Kaitlyn Lurker Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above