CDCII

Clinical Data Coordinator II- 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.

We are currently seeking a Clinical Data Coordinator II to join our diverse and dynamic team. As a Clinical Data Coordinator 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 

• Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.

• Manage clinical and third-party data reconciliation based on edit specifications and data review plans.

• Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.

• Address data related questions and recommend potential solutions.

• Identify root cause to systematically resolve data issues.

Your profile 

• Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.

• Intermediate knowledge of clinical data management within the pharmaceutical or biotechnology industry.

• Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).

• Strong attention to detail and the ability to work effectively in a fast-paced environment.

• Excellent communication skills and the ability to collaborate with cross-functional teams.

• Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.

Nous recherchons actuellement un(e) Clinical Data Coordinator II pour rejoindre notre équipe diversifiée et dynamique. En tant que Clinical Data Coordinator 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 au développement de traitements et de thérapies innovants.

Vos missions

• Assister le/la Data Management Study Lead dans la maintenance des eCRF, des spécifications de validation des données et des procédures spécifiques à l’étude.

• Gérer la réconciliation des données cliniques et des données tierces conformément aux spécifications d’édition et aux plans de revue des données.

• Suivre et communiquer l’état d’avancement des études et des indicateurs de tâches aux data scientists cliniques, à l’équipe projet et au management fonctionnel.

• Traiter les questions liées aux données et recommander des solutions potentielles.

• Identifier les causes racines afin de résoudre systématiquement les problématiques de données.

Votre profil

• Diplôme de niveau licence (Bachelor) dans un domaine pertinent, tel que les sciences de la vie ou la santé.

• Connaissances intermédiaires en gestion des données cliniques dans l’industrie pharmaceutique ou biotechnologique.

• Maîtrise des logiciels et systèmes de gestion des données (par exemple Medidata, Oracle RDC ou équivalent).

• Sens aigu du détail et capacité à travailler efficacement dans un environnement dynamique et exigeant.

• Excellentes compétences en communication et aptitude à collaborer avec des équipes transverses.

• La connaissance des lignes directrices et normes réglementaires (par exemple ICH-GCP) est un atout.

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