Associate Project Manager
Como Associate Project Manager, apoyarás la coordinación y gestión de ensayos clínicos. El puesto ofrece desarrollo profesional y un entorno colaborativo.
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Más de 90.000 ofertas activasEn remoto, Poland, Warsaw·Añadida hace 2 meses (comprobada el 19 oct)
63 ofertas abiertas
Esta oferta está publicada en inglés.
Site Contracts Lead - Home or office based
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Site Contracts Lead at ICON, you will oversee and coordinate the preparation, negotiation, and execution of clinical trial agreements and budgets for assigned studies or portfolios.
You will oversee contract management workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
You will have solid contract management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
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:
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
ICON es una organización de investigación clínica (CRO) que ofrece servicios subcontratados de desarrollo clínico y comercialización a las industrias farmacéutica, biotecnológica y de dispositivos médicos. La empresa se describe como la organización de investigación clínica líder en el mundo y opera a escala global, con empleados en 119 ubicaciones en 53 países.
Sus servicios abarcan operaciones clínicas y científicas, ensayos clínicos descentralizados, servicios clínicos tempranos y de laboratorio, imagen médica, asuntos regulatorios, consultoría, comercialización, redacción médica, biometría y medidas de resultados. ICON trabaja en sectores que incluyen la farmacéutica, la biotecnología, los dispositivos médicos, el gobierno y la salud pública, y en áreas terapéuticas como la oncología, la cardiovascular, el sistema nervioso central, las vacunas y las enfermedades raras y huérfanas.