... examine ways to enhance overall clinical trial performance.Facilitate communication between clinical sites and other Abbott clinical staff (e.g., CSL, CRA, ... : technical, protocol, standard of care, clinical trial reimbursement, etc.Responsible for product ...
... vendors required for conduct of clinical trialsDirect Manage necessary clinical trial approvals from IRBs ECs, and ...
... documentation and filing of a clinical trial and acts as a pivotal point of contact for the entire clinical trial team. The following list provides ...
... , training and experience.Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements, i.e. ...
... in the domains relevant to Clinical Psychology. The courses can be ... seminars, and individual supervision of clinical or research internships and thesis ... topics. The ideal candidate links clinical research to societal conditions and ...
... interface between our client and clinical trial sites across all development programs, working closely with Clinical Development & Clinical Operations Advising and participating in ...
... as a key interface with clinical trial sites across all development programs, working closely with Clinical Development and Clinical Operations. Additionally, you will collaborate ...
... Acts as a Clinical Trial Regulatory Manager (CTRM) on global ... Prepares and maintains core clinical trial submission dossiers in accordance with ... Investigational Medicinal Product Dossier, clinical trial justifications with minimum support of ...
... Degree in natural sciences or clinical sciences Several years of professional experience in clinical trial management and or clinical research Experience within the pharmaceutical ...
... relevant for the conduct of clinical trials Ideally experience in the field of vaccine development Supervisory managerial experience in clinical development including supervision of CROs ...