ICON Job Opportunities: Apply Now for Multiple Positions

We are thrilled to announce that ICON, a global provider of outsourced development and commercialization services to the pharmaceutical, biotechnology, and medical device industries, is opening up multiple job opportunities. If you’re looking to make a significant impact in the healthcare industry, one of these positions might be perfect for you.

Job Listings

PV Associate/Sr PV Associate

As a PV Associate/Sr PV Associate, you will be responsible for monitoring and assessing the safety of pharmaceutical products. This role requires a keen eye for detail and a strong understanding of pharmacovigilance practices. If you have experience in drug safety and are looking to advance your career, apply now.

Supervisor, CTA

The Supervisor, CTA position involves overseeing clinical trial activities, ensuring compliance with regulatory requirements, and managing a team of clinical trial associates. Strong leadership and organizational skills are essential for this role. Apply today if you have a background in clinical research and a passion for guiding teams to success.

Clinical Research Associate I/II

As a Clinical Research Associate I/II, you will conduct site monitoring visits, ensure clinical trials are conducted according to protocol, and maintain regulatory documentation. This role is ideal for candidates with experience in clinical trials and a meticulous approach to ensuring data integrity. Apply now to join a dynamic team dedicated to advancing medical research.

Data Scientist (Real-World Evidence & Medical Claims) – Homebased

The Data Scientist (Real-World Evidence & Medical Claims) role involves analyzing large datasets to generate insights that support clinical and commercial decision-making. This homebased position requires expertise in data analysis, statistical modeling, and a solid understanding of medical claims data. If you have a passion for leveraging data to drive healthcare advancements, apply today.

Site Management Administrator

As a Site Management Administrator, you will support site management activities, including site selection, initiation, and close-out processes. This role requires excellent organizational skills and the ability to manage multiple tasks simultaneously. Apply now if you are detail-oriented and have experience in clinical site management.

TMF Lead

The TMF Lead will be responsible for overseeing the Trial Master File (TMF) process, ensuring that all documentation is complete, accurate, and compliant with regulatory standards. This role demands strong project management skills and experience in clinical trial documentation. Apply today if you are meticulous and have a background in managing TMF processes.

We have 6 jobs, that could be just what you are looking for.

PV Associate/Sr PV Associate

Clinical Research Associate I/II

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Data Scientist (Real-World Evidence & Medical Claims) – Homebased

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