As a Site Care Partner, you will join the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence.
What you will be doing:
- Responsible for relationship building and operational oversight of the site.
- Provide study support on escalated site issues related to study delivery by coordinating communications and resolution efforts (e.g., vendor, site contracts, and payment issues).
- Ensure the strategy/approach for IP and ancillary supplies for sites and country requirements throughout the study lifecycle.
- Accountable for effective site recruitment planning and delivery, aligned with global, country, and local targets; support enrollment and respond to recruitment issues from investigators.
- Maintain regular communication with investigator sites to gather status updates and drive delivery to study goals (recruitment, data entry timelines).
- Partner with local RA/CTRO/SAP to ensure timely completion of country/local registry when applicable.
En quoi consistera votre travail:
- Accompagner les centres d’étude dans leur activation et dans les activités de l’étude, du début à la clôture.
- Maintenir des communications régulières pour obtenir des mises à jour et des commentaires sur leur progrès et rendement.
- Agir en tant que personne-ressource principale pour toutes questions concernant les centres d’étude, en assurant la liaison avec les équipes appropriées.
- Informer et éduquer les centres d’étude sur les opportunités de participation aux études de recherche du portefeuille de Pfizer.
- Diriger la planification du recrutement des centres conformément au plan mondial et aux objectifs locaux.
You are:
Education
- Bachelor’s degree or RN in a related field or equivalent, with at least 5 years of experience.
- Proficiency in the local language preferred; English required.
Skills and Technical Competencies
- Knowledge of Good Clinical Practice/ICH Guidelines and regulatory requirements.
- Good computer skills and adaptability to new technologies.
- Effective communication, presentation, and interpersonal skills.
- Ability to travel up to 75% regularly.
- Networking and relationship-building skills.
- Ability to manage cross-functional relationships and projects.
- Effective communication with internal and external stakeholders.
- Ability to adapt to evolving technologies and processes.
- Knowledge of country-specific GCP requirements.
Ce que vous devez posséder:
- Knowledge of quality and regulatory requirements for applicable countries.
- Experience with site activation, clinical trial monitoring, and regulatory environments.
- Proven success in scientific, technical, or administrative roles.
- Strong networking and relationship development skills.
- Ability to manage interdepartmental projects and processes.
- Effective communication skills with stakeholders.
- Adaptability to technological and procedural changes.
What ICON can offer you:
Our success depends on our people. We prioritize building a diverse culture that rewards performance and nurtures talent. In addition to a competitive salary, ICON offers various benefits focused on well-being and work-life balance, including health insurance, retirement plans, employee assistance programs, life assurance, and flexible benefits.
Visit our careers website for more: https://careers.iconplc.com/benefits
ICON is committed to inclusion and providing an accessible environment for all candidates. We do not discriminate and provide accommodations for applicants with disabilities. Learn more: https://careers.iconplc.com/reasonable-accommodations
Interested but unsure if you meet all requirements? We encourage you to apply, as you might be the perfect fit for this or other roles at ICON.