To lead Local Study Team(s) (LSTs) at country level to deliver committed components of clinical studies according to agreed resources, budget and…
\ \ JOB DESCRIPTION Minimum Qualifications & Experience: Graduate in a clinical or life sciences related field. Relevant experience/qualifications in allied professions…
\ \ Study Start Up Specialist\
\ Job Description 100,000+ That\\\'s how many patients participate in our clinical trials at any given time. GCO is Novartis\\\' powerhouse of…
\ At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare…
\ \ The Associate Start up Project Manager oversees and manages the start up phase of domestic and/or international clinical trials, primarily…
\ \ At Lilly, we unite caring with discovery to make life better for people around the world. We are a global…
\ \ General Tasks Responsible for maintaining awareness of regulatory legislation, guidance and practice, ICH/GCP and relevant Sponsor requirements Take ownership in…
\ \ The Associate Start up Project Manager oversees and manages the start up phase of domestic and/or international clinical trials, primarily…
b\'\ General Tasks\ \ Responsible for maintaining awareness of regulatory legislation, guidance and practice, ICH/GCP and relevant Sponsor requirements\ Take ownership in…
\ Job Description: About the Position: The Regulatory Start Up Associate is primarily responsible for planning, preparation, review of country and site…
b\'\ The Associate Start up Project Manager oversees and manages the start up phase of domestic and/or international clinical trials, primarily on…
\ \ Study Start Up Specialist\
\ Overview ICON plc is a world leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research…
\ \ \ \ 100,000+ That\\xe2\\x80\\x99s how many patients participate in our clinical trials at any given time. GCO is Novartis\\xe2\\x80\\x99 powerhouse…
\ Job Description Associate Director, Regulatory Affairs The Associate Director, Regulatory Affairs role reports to the SSDM Director/(Sr) Director and will partner…
\ \ ICON plc is a world leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research…
\ Job Description: About the Opportunity: The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial…
\ JOB DESCRIPTION About the Opportunity: The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial…
\ Job Description: Minimum Qualifications & Experience: Graduate in a clinical or life sciences related field. Relevant experience/qualifications in allied professions may…