Job Description
Clinical Data Coordinator- 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 I to join our diverse and dynamic team. As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
**What you will be doing **
+ Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.
+ Review clinical and third-party data based on edit specifications and data review plans.
+ Issue clear, accurate, and concise queries to investigational sites.
+ As required, communicate effectively with peers, clinical data scientist and functional management.
+ Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.).
**Your profile **
+ Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
+ Basic kNwledge of clinical data management within the pharmaceutical or biotechNlogy 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.
+ KNwledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
Nous recherchons actuellement un(e) **Coordinateur(trice) des Données Cliniques I** pour rejoindre notre équipe diversifiée et dynamique. En tant que Coordinateur(trice) des Données Cliniques 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 Responsable de l’Étude en Data Management dans le développement des eCRF, des spécifications de validation des données et des procédures spécifiques à l’étude.
+ Examiner les données cliniques et les données de tiers conformément aux spécifications de contrôle et aux plans de revue des données.
+ Émettre des demandes de clarification (queries) claires, précises et concises à destination des centres investigateurs.
+ Selon les besoins, communiquer efficacement avec les pairs, les data scientists cliniques et le management fonctionnel.
+ Réaliser d’autres activités liées au projet afin de garantir le respect des délais de l’étude (par exemple : classement et archivage de la documentation de l’étude, envoi des queries aux centres investigateurs pour résolution, etc.).
**Votre profil**
+ Diplôme de niveau licence (Bachelor) dans un domaine pertinent, tel que les sciences de la vie ou la santé.
+ Connaissances de base en gestion des données cliniques au sein de l’industrie pharmaceutique ou biotechnologique.
+ Familiarité avec les logiciels et systèmes de data management (par exemple : Medidata, Oracle RDC ou équivalent).
+ Forte attention aux détails 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 directives et normes réglementaires (par exemple : ICH-GCP) constitue un atout.
Si tu le souhaites, je peux aussi l’adapter à un **style plus corporate** , **plus concis** , ou **aligné avec les standards ICON** .
**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 (https://careers.iconplc.com/benefits) 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 (https://careers.iconplc.com/reasonable-accommodations)
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 (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
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 I to join our diverse and dynamic team. As a Clinical Data Coordinator at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of inNvative treatments and therapies.
**What you will be doing **
+ Assist Data Management Study Lead in development of eCRF, Data Validation Specifications, and Study Specific Procedures.
+ Review clinical and third-party data based on edit specifications and data review plans.
+ Issue clear, accurate, and concise queries to investigational sites.
+ As required, communicate effectively with peers, clinical data scientist and functional management.
+ Perform other project activities as required in order to ensure that study timelines are met (for example, filing and archiving of study documentation, dispatching of queries to investigator sites for resolution, etc.).
**Your profile **
+ Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.
+ Basic kNwledge of clinical data management within the pharmaceutical or biotechNlogy 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.
+ KNwledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus.
Nous recherchons actuellement un(e) **Coordinateur(trice) des Données Cliniques I** pour rejoindre notre équipe diversifiée et dynamique. En tant que Coordinateur(trice) des Données Cliniques 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 Responsable de l’Étude en Data Management dans le développement des eCRF, des spécifications de validation des données et des procédures spécifiques à l’étude.
+ Examiner les données cliniques et les données de tiers conformément aux spécifications de contrôle et aux plans de revue des données.
+ Émettre des demandes de clarification (queries) claires, précises et concises à destination des centres investigateurs.
+ Selon les besoins, communiquer efficacement avec les pairs, les data scientists cliniques et le management fonctionnel.
+ Réaliser d’autres activités liées au projet afin de garantir le respect des délais de l’étude (par exemple : classement et archivage de la documentation de l’étude, envoi des queries aux centres investigateurs pour résolution, etc.).
**Votre profil**
+ Diplôme de niveau licence (Bachelor) dans un domaine pertinent, tel que les sciences de la vie ou la santé.
+ Connaissances de base en gestion des données cliniques au sein de l’industrie pharmaceutique ou biotechnologique.
+ Familiarité avec les logiciels et systèmes de data management (par exemple : Medidata, Oracle RDC ou équivalent).
+ Forte attention aux détails 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 directives et normes réglementaires (par exemple : ICH-GCP) constitue un atout.
Si tu le souhaites, je peux aussi l’adapter à un **style plus corporate** , **plus concis** , ou **aligné avec les standards ICON** .
**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 (https://careers.iconplc.com/benefits) 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 (https://careers.iconplc.com/reasonable-accommodations)
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 (https://wd3.myworkday.com/icon/d/task/1422$1235.htmld) to apply
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