... Medical Advisor on clinical trials • Experience working on Global Clinical Trials including Clinical Trial Design, Data & Reporting • Knowledge of both SSO Operational Clinical Trials and Medical Affairs • Operations ... our associates that drive us each day ...
... years of experience as a Clinical Research Associate, with a focus on ophthalmology trials. In-depth knowledge of GCP, ICH guidelines, and regulatory requirements related to clinical trials. Strong communication and interpersonal skills. ...
... precision medicine by combining novel clinical trial designs, industry-leading operational and ... and a say in how clinical trials are runYou plan ahead, but ... and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights ...
... precision medicine by combining novel clinical trial designs, industry-leading operational and ... and a say in how clinical trials are runYou plan ahead, but ... and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights ...
... Local Study Team (LST) the Clinical Trial Assistant ensures quality and consistency of study deliverables to time, cost and quality objectives.Essential Functions:Assist Clinical Research Associates (CRAs) and Regulatory and Start- ...
... minimum of 1 year of clinical trial monitoring experience is preferred, however, ... and regulations, assigned protocols and associated protocol specific procedures including monitoring ...
... of EU clinical trial applications for the EEA region for internally managed trials. The CTSC collaborates with global ... submissions or multinational clinical trial submissions under the EU Clinical Trial Directive. Demonstrated experience being solutions ...
... every successful clinical trial. Working alongside brilliant minds across ... experience as a Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role 3+ years’ experience as a Clinical Research Associate Willingness to travel We love ...
... legal and regulatory standards Conduct clinical trials according to ICH GCP local ... their medical responsiblity of the clinical trial. Review and follow Scientific Advice ...
... standards • Conduct clinical trials according to ICH GCP, local ... finalization of the clinical trial • Medical monitoring of the trials • Oversee a lab report review, ... responsiblity of the clinical trial. • Review and follow Scientific Advice ...