... Clinical Research Associate I Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial ... ensuring regulatory, ICH-GCP and or Good ...
... Research Associate (Lead CRA) to join our diverse and dynamic team. As a Lead CRA at ICON, you will play a pivotal role in overseeing and managing clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements ...
... the study process, audits and regulatory inspections, according to company policies ... from local language, as required. Regulatory and Site Start Up: Collects, ... effective publishing and delivery to regulatory authorities. Budgeting, Agreements and Payments: ...
... positive “can-do” attitude. The Associate Counsel is primarily responsible for ... revenue-generating customer agreements. The Associate Counsel will also provide legal ... it is expected that the Associate Counsel will establish productive relationships ...
... product expertise across Medical Affairs. You will work with Therapeutic ... operational needs within Medical Affairs. Leads a Medical Affairs Excellence Matrix forum to establish ... . 5+ years of Medical Affairs Leadership experience Experience building and ...
... Biotech Solutions Clinical Research Associate I II Sr. ... a Clinical Research Associate I II Sr. at ICON, you will play a pivotal role in monitoring clinical trials, ensuring compliance with study protocols and regulatory requirements, and contributing to the ...
... treatments. From clinical trials to regulatory, consulting, and market access, our ... are met. The Site Contract Associate is responsible for the coordination ... applicable ICH-GCP Guidelines, local regulatory requirements, and PAREXEL WSOPs and ...
... treatments. From clinical trials to regulatory, consulting, and market access, our ... are met. The Site Contract Associate is responsible for the coordination ... applicable ICH-GCP Guidelines, local regulatory requirements, and PAREXEL WSOPs and ...
... Responsibilities and Study Conduct Ensuring regulatory, ICH-GCP and protocol compliance. ... and verifies issues or risks associated with blinded or randomized information ... skills relating to colleagues and associates, both inside and outside of ...
... Pharma Solutions Clinical Research Associate I II ICON plc ... a Clinical Research Associate I II at ICON, you will play a pivotal role in monitoring clinical trials, ensuring compliance with study protocols and regulatory requirements, and contributing to the ...