Local Trial Manager
... site-level goal setting and study-specific deliverables for clinical sites within their country(ies) Contribute to deliver and or lead CRA, Investigator and Study Coordinator training Manage, oversee and monitor ...
... site-level goal setting and study-specific deliverables for clinical sites within their country(ies) Contribute to deliver and or lead CRA, Investigator and Study Coordinator training Manage, oversee and monitor ...
... the CTMRT Accountable to the Clinical Study Team for: review of medical- ... strategies in collaboration with the Clinical Study Team as appropriateSupport the Data ... neededMay participate in writing initial Clinical Study Report narratives or narratives in ...
... -functional team Review and provide clinical operations input into relevant clinical documents such as the protocol, investigator brochure, regulatory documents, clinical study reports and other documents and ...
... patient recruitment, and overall study success. Build advancing capabilities at Topography’s clinical trial sites, working with internal ... + years of experience in Clinical Research, serving as a Clinical Research Coordinator or similar role, with advancing ...
... closely collaborating with the Clinical Operations Lead and or assigned Clinical Trial Managers to execute clinical studies. Drafting and distributing essential site ... the appropriate conduct of clinical studies Excellent verbal and written communication ...
... setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures ...
... setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures ...
... setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures ...
... : Provide medical monitoring to multiple clinical trials.Lead project teams to design and implement clinical studies.Write protocols, investigator brochures, clinical study reports and review clinical trial documents.Conduct investigator meetings ...
... the conduct and oversight of clinical studies in academia or industry is ... submissions, abstracts, manuscripts and publications, clinical study reports, clinical pharmacology translational medicine plans, etc. ...