Remote Jobs at ICON plc
Find your next remote opportunity · 93 Open Positions
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.
We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries.
We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Project Manager
Project Manager leading and coordinating healthcare projects at ICON. Delivering projects on time, within budget, and to quality standards while managing cross-functional teams.
Global Pharmacovigilance Excellence Lead
Global Pharmacovigilance Excellence Lead overseeing safety and efficacy of clinical trials for new medicines. Responsible for leading transformational projects and ensuring compliance in GPV activities.
Senior Manager – Biosample Operations Lead
Senior Manager Biosample Operations leading strategic biosample management in clinical studies at ICON. Focused on operational feasibility and compliance for new medicines.
Senior Study Start Up Associate
Senior Study Start Up Associate at ICON managing clinical research site start-up processes in a fast-paced environment. Leading site activation tasks and ensuring regulatory compliance with top-notch patient safety standards.
Senior Medical Writer
Principal Medical Writer at ICON leading the development of regulatory and clinical documents. Collaborating across teams to ensure high-quality outputs and adherence to standards.
RBSM – CRM
Central Monitor ensuring quality and integrity of clinical trial data through monitoring at ICON. Collaborating cross-functionally and utilizing advanced data analytics tools for effective monitoring.
Grants Specialist
Grants Specialist for ICON managing grant applications, collaborating with internal stakeholders on proposals. Ensuring compliance and tracking activities in a global healthcare setting.
Patient Recruitment Lead
As a Patient Recruitment Lead at ICON, you'll drive patient recruitment strategies for clinical trials. Collaborate with teams to enhance recruitment efforts and ensure compliance with regulatory standards.
Study Delivery Specialist
Site Management Associate I at ICON supporting clinical trial management and site monitoring activities for a global healthcare organisation. Delivering clinical research work and collaborating with cross-functional teams.
Contract Analyst II
Contract Analyst II at ICON managing clinical trial agreements and vendor contracts. Collaborating with cross-functional teams and ensuring compliance with legal and regulatory standards.
Clinical Data Manager
Senior Clinical Data Manager at ICON responsible for designing and analyzing clinical trials. Collaborating with teams to manage data quality and mentoring junior coordinators.
Site Management Associate II
SMA II at ICON supporting clinical trial site management, ensuring compliance with regulations and protocols. Collaborating with teams to enhance site performance and mentoring staff for development.
Site Contracts Lead
Site Contracts Lead overseeing and coordinating clinical trial agreements and budgets for assigned studies at ICON. Collaborating with internal teams to ensure quality and timeliness in deliverables.
Clinical Trial Manager
Clinical Trial Manager at ICON managing clinical trial operations and ensuring quality outcomes across clinical programmes. Collaborating with teams and ensuring compliance with regulations.
Senior Contract Analyst
Senior Contract Analyst at ICON managing contractual agreements and compliance in a global healthcare intelligence organization. Collaborating with stakeholders to review and negotiate contracts for clinical research projects.
Clinical Research Associate
Clinical Research Associate analyzing clinical trials and contributing to innovative treatments at ICON. Collaborating with investigators and ensuring compliance through monitoring activities in Romania.
Senior Clinical Trial Manager – Oncology
Senior Clinical Trial Manager at ICON managing clinical trial operations activities and supporting teams to deliver quality outcomes across clinical programmes.
Study Start-up Associate II
Study Start Up Associate II at ICON leading the initiation of clinical trials. Ensuring compliance with regulatory requirements and advancing innovative treatments and therapies.
Senior Clinical Trial Manager
Senior Clinical Trial Manager managing clinical trial operations and team capabilities at ICON. Focused on budget oversight, study performance, and relationship building with stakeholders.
Senior Contract Study Manager
Contracts Analyst reviewing and analyzing contracts related to clinical trials at ICON. Collaborating with teams to manage contract risks and ensure compliance with regulations.