As a Clinical Research Coordinator you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Opthamology experience is required. What You Will Be Doing. Maintain test and control article inventory throughout the study, and perform test and control article reconciliation at study completion. Manage the investigator file (ISF) and other regulatory documents throughout the study ...
If you are seeking a leadership position in clinical research data management with one of the largest & most reputable global clinical research organizations, please apply to this sponsor aligned position with ICON LLC (global CRO). As a Global Data Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will provide data management oversight and accountability f...
This position is onsite in Wilmington, DE - no relocation. The Staff Scientist will play a critical role within the Antibody Discovery group by performing essential functions to support the early-phase screening of antibody candidates. Responsibilities include protein QC using analytical methods, maintaining mammalian cell lines relevant to cell-binding assays, preparing normalized antibody stocks, and stamping these into assay plates using high-...
If you are seeking a leadership position in clinical research data management with one of the largest & most reputable global clinical research organizations, please apply to this sponsor aligned position with ICON LLC (global CRO). As a Global Data Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will provide data management oversight and accountability f...
If you are seeking a leadership position in clinical research data management with one of the largest & most reputable global clinical research organizations, please apply to this sponsor aligned position with ICON LLC (global CRO). As a Global Data Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will provide data management oversight and accountability f...
If you are seeking a leadership position in clinical research data management with one of the largest & most reputable global clinical research organizations, please apply to this sponsor aligned position with ICON LLC (global CRO). As a Global Data Manager you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence. You will provide data management oversight and accountability f...
As a Senior Specialist, Medical Operations, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What You Will Be Doing. Essential Document Maintenance – ensures all appropriate documentation in support of a proposal has been collected and filed correctly within the document repository systems on an ongoing basis. Pharmacovigilance Compliance activities - IAL distribution...
ICON is hiring a Clinical Scientist II (Flow Cytometry) for our Wilmington, DE lab location. If qualified and interested, please apply today. Qualifications. 2 years clinical Lab Work with. Flow Cytometry. Testing Techniques (western Blot, qPCR, ELISA etc. B.Sc. or Master’s degree. Candidates with hands-on experience in flow cytometry and flow cytometry data analysis software will be preferred. Candidates with a background in cancer and/or myeloi...
ICON Strategic Solutions is currently hiring for a Technical ePRO Project Manager for one of our client dedicated teams. This is a hybrid based role and will require you to be in office 3 days/week in either Rahway, NJ or West Point, PA. The in office requirement will drop to 2 days/week after 6 months of proven work history. This role will be responsible for. Manage translation process and timelines with vendors. Kickoff ePRO development. Draft/...
As a Optometrist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. This position is located in Fort Worth Texas. Location. 900 Jerome St. Suite 300 Ft. Worth, TX 76104. Hours will be M-F 9-6. What you will be doing. Responsible for the safety of all clinical subjects participation in clinical studies and conduct of the clinical trials and data integrity. Knowledge of s...
