Senior Project Manager - DCT
- Canada, Multiple US Locations
- Clinical Project Management
- ICON Full Service & Corporate Support
- Remote
TA Business Partner
- Full Service Division
About the role
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ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
Role: DCT Senior Project Manager
Location: US & Canada (Remote)
Recognize, exemplify, and adhere to ICON's values, which center on our commitment to People, Clients and Performance.
In order to be qualified for this role you must have experience one or more of the following:
eConsent
Telehealth
ePro
eCOA
Direct to Patient (DTP)
home nursing
digital health platform
- Stay abreast of industry changes, including regulatory guidance pertaining to DCTs and new technology/vendor offerings to support DCTs.
• Lead the planning and implementation of cross-functional Decentralized Clinical Trial project(s).
• Facilitate the definition of project scope, goals and deliverables
• Define project tasks and resource requirements.
• Develop full-scale cross-functional project plans.
• Assemble and coordinate project staff
• Manage project budget
• Plan and schedule project timelines
• Develop and Manage Risk Mitigation Strategies for projects
• Track project deliverables using appropriate tools
• Provide direction and support to project team
• Quality assurance
• Constantly monitor and report on progress of the project to all stakeholders
• Present reports defining project progress, problems and solutions.
• Implement and manage project changes and interventions to achieve project outputs
• Project evaluations and assessment of results
To be successful in the role, you will have:
Bachelor’s Degree in science, business, medicine or equivalent degree
Project Management or equivalent (PMI certification) is desirable
Experience managing projects with Decentralized Clinical Trial elements is preferred
At least 1 year PM experience within clinical research and study operations
Experience in working on a wide range of therapeutic indications; Late Phase experience preferred
Comprehensive knowledge of ICH-GCP
Strength in communication, planning, decision-making, negotiation, conflict management and time management skills
Willingness to travel up to 25% as needed
Benefits of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.
We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.
ICON is an equal opportunity and inclusive employer and 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 through the form below.
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ICON plc est un chef de file mondial en matière de soins de santé intelligents et de recherche clinique. De la molécule au médicament, nous faisons progresser la recherche clinique en offrant des services externalisés aux entreprises pharmaceutiques, biotechnologiques et d’équipement médical, ainsi qu’aux organismes gouvernementaux et de santé publique.
En plaçant nos patient(e)s au cœur de toutes nos activités, nous contribuons à accélérer le développement de médicaments et de dispositifs, qui sauvent des vies et améliorent la qualité de vie des patient(e)s.
Nos employé(e)s sont le fer de lance de notre culture et constituent la force motrice de notre succès. Les employé(e)s d’ICON ont pour mission de réussir et sont animé(e)s d’une passion qui garantit que ce que nous faisons, nous le faisons bien.
Rôle : Chef de projet sénior DCT
Lieu : États-Unis et Canada (télétravail)
Reconnaître, incarner et respecter les valeurs d’ICON qui sont axées sur notre engagement envers les gens, les clients et le rendement.
En tant que membre du personnel, l’employé(e) doit reconnaître l’importance de notre culture d’amélioration des processus, et la soutenir en mettant l’accent sur leur simplification, en ajoutant de la valeur à notre entreprise et en répondant aux besoins des clients.
• Diriger la planification et la mise en œuvre de projets d'essais cliniques décentralisés et interfonctionnels.
• Faciliter la définition de la portée, des objectifs et des livrables du projet
• Faciliter la définition de la portée, des objectifs et des livrables du projet.
• Élaborer des plans de projet interfonctionnels à grande échelle.
• Rassembler et coordonner le personnel du projet
• Gérer le budget du projet
• Organiser et planifier les échéanciers du projet
• Développer et gérer des stratégies d'atténuation des risques pour les projets
• Suivre les livrables du projet à l'aide d'outils appropriés
• Guider et apporter un soutien à l'équipe de projet
• Assurance qualité
• Surveiller et faire part en continu de l'avancement du projet à toutes les parties prenantes
• Présenter des rapports définissant l'avancement du projet, les problèmes et les solutions.
• Mettre en œuvre et gérer les changements et les interventions du projet pour atteindre les résultats du projet
• Évaluations de projet et appréciation des résultats
- Se tenir informé des changements de l'industrie, y compris les directives réglementaires relatives aux DCT et aux nouvelles offres de technologie/fournisseur pour prendre en charge les DCT.
Ce dont vous avez besoin pour réussir dans ce poste :
- Baccalauréat en sciences, commerce, médecine ou diplôme équivalent
- Gestion de projet ou l'équivalent (certification PMI) est souhaitable
- Une expérience de la gestion de projets avec des éléments d'essais cliniques décentralisés est souhaitable
- Au moins 1 an d'expérience en tant que manager de projet dans la recherche clinique et les opérations d'étude
- Expérience professionnelle sur un large éventail d'indications thérapeutiques; Expérience en phase tardive souhaitée
- Connaissance approfondie des BPC de l’ICH.
- Solides compétences en communication, organisation, prise de décision, négociation, gestion des conflits et gestion du temps
- • Capacité de voyager jusqu'à 25 % du temps si besoin
Les avantages à travailler pour ICON:
Notre réussite est tributaire de la connaissance, des capacités et de la qualité de nos employé(e)s. C'est la raison pour laquelle nous nous sommes donnés pour priorité de bâtir une culture qui récompense les hautes performances et nourrit les talents.
Nous offrons des rémunérations globales très concurrentielles. Et pour les conserver, nous les comparons régulièrement à celles de nos concurrents. Nos primes annuelles reflètent l’atteinte des objectifs de rendement — tant les nôtres que les vôtres.
Nous offrons également une vaste gamme d’avantages sociaux aux employé(e)s et à leur famille ainsi que des régimes de retraite concurrentiels — et des avantages connexes comme l’assurance vie. Vous pouvez donc économiser et planifier en toute confiance les années à venir.
Mais au-delà de la rémunération concurrentielle et d’un programme d’avantages sociaux complet, vous bénéficierez d’un environnement où vous serez encouragé(e) à satisfaire votre sentiment d’utilité et à susciter des changements durables.
ICON est un employeur inclusif, souscrivant au principe de l’égalité d’accès à l’emploi, et s’engage à offrir un milieu de travail sans discrimination ou harcèlement. Tous et toutes les candidat(e)s qualifié(e)s bénéficieront d’une considération égale pour l’emploi, sans égard pour l’ethnicité, la couleur, la religion, le sexe, l’orientation sexuelle, l’identité de genre, l’origine nationale, le handicap ou le statut d’ancien combattant protégé.
Si, en raison d’un problème de santé ou d’un handicap, vous avez besoin d’un aménagement adéquat pour une partie du processus de candidature, ou dans le but d’exécuter les fonctions essentielles d’un poste, veuillez nous en aviser en remplissant le formulaire ci-dessous.
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Application process
Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.
Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.
One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.
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