Key Facts

Remote From:

Full time

Mid-level (2-5 years)

English

Hard Skills

Building Inspections Protocol Implementation Conformance Statement Clinical Study Design Patient Safety Language Interpretation Protocol Analysis Data Integrity Clinical Study Design Clinical Trial Planning FDA Regulations Query Planning

Other Skills

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Organizational Skills
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Teamwork
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Detail Oriented
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Communication

Roles & Responsibilities

Bachelor's degree in a scientific or healthcare-related field
Minimum of 2 years of experience as a Clinical Research Associate
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines
Strong organizational and communication skills, with attention to detail; ability to work independently and collaboratively

Requirements:

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process
Collaborating with investigators and site staff to facilitate smooth study conduct
Performing data review and resolution of queries to maintain high-quality clinical data

ICON plc

Pharmaceuticals

About ICON plc

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.

Company type: XLarge

Industry: Pharmaceuticals

Founded: 2018

Company size: 10001

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Job description

Clinical Research Associate, Sponsor Dedicated

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

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.

What you will be doing

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

Collaborating with investigators and site staff to facilitate smooth study conduct.

Performing data review and resolution of queries to maintain high-quality clinical data.

Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your profile

Bachelor's degree in a scientific or healthcare-related field.

Minimum of 2 years of experience as a Clinical Research Associate.

In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

Strong organizational and communication skills, with attention to detail.

Ability to work independently and collaboratively in a fast-paced environment.
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

ICON plc est une organisation de premier plan à l’échelle mondiale dans le domaine de l’intelligence en santé et de la recherche clinique. Nous sommes fiers de favoriser un environnement inclusif qui stimule l’innovation et l’excellence, et nous vous invitons à nous rejoindre dans notre mission visant à façonner l’avenir du développement clinique.

Nous recherchons actuellement un(e) Attaché(e) de Recherche Clinique (ARC) II pour rejoindre notre équipe diversifiée et dynamique. En tant qu’ARC II chez ICON, vous jouerez un rôle clé dans la conception et l’analyse des essais cliniques, l’interprétation de données médicales complexes et la contribution à l’avancement de traitements et de thérapies innovants.

Vos missions

Réaliser des visites de qualification des sites, de mise en place, de suivi et de clôture des essais cliniques.
Garantir le respect du protocole, l’intégrité des données et la sécurité des patients tout au long du processus de l’étude.
Collaborer avec les investigateurs et le personnel des sites afin de faciliter le bon déroulement des études.
Effectuer la revue des données et la résolution des queries afin de maintenir des données cliniques de haute qualité.
Contribuer à la préparation et à la révision de la documentation des études, notamment les protocoles et les rapports d’études cliniques.

Votre profil

Licence ou Bachelor dans un domaine scientifique ou lié à la santé.
Minimum de 2 ans d’expérience en tant qu’Attaché(e) de Recherche Clinique.
Excellente connaissance des processus des essais cliniques, de la réglementation et des lignes directrices ICH‑GCP.
Solides compétences organisationnelles et de communication, avec un grand souci du détail.
Capacité à travailler de manière autonome tout en collaborant efficacement dans un environnement dynamique et exigeant.
Disponibilité pour voyager au moins 60 % du temps (à l’international et au niveau national – déplacements en avion et en voiture) et possession d’un permis de conduire valide.

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