and Delivery. Manages a project as a project manager overseeing interdisciplinary clinical research studies and ensures compliance... and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations such as site...
. Escalates to the project manager any risks to clinical trial management deliverables (timeline, quality and budget... compliance and delivery according to protocol, SOPs, ICH GCP and country regulations This may include data management, study...
The Clinical Trial Manager II (CTM II), Dermatology & Rheumatology, is responsible for the operational management... but is not limited to clinical research associate (CRA) training, identification of quality issues related to site performance...
Dedicated****Job Overview**The Quality Manager provides services within the assigned country/countries or region that ensure... an integrated and comprehensive quality and compliance approach for clinical trials in close collaboration with local and global...
within the assigned country/countries or region that ensure an integrated and comprehensive quality and compliance approach...), International Conference on Harmonization (ICH), Good Clinical Practice (GCP), applicable regulatory requirements, quality...
Dedicated****Job Overview**The Quality Manager provides services within the assigned country/countries or region that ensure... an integrated and comprehensive quality and compliance approach for clinical trials in close collaboration with local and global...
within the assigned country/countries or region that ensure an integrated and comprehensive quality and compliance approach...), International Conference on Harmonization (ICH), Good Clinical Practice (GCP), applicable regulatory requirements, quality...
, consolidate, and communicate strategic insights from country/regional teams to optimize clinical development and business...The Position Provides strategic leadership, functional expertise, and operational oversight for clinical trial...
per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements... contracts, including tracking and data in associated systems Ensure quality and completeness of TMF for assigned clinical trials...
per established project team goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements... within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead...
Leadership Drive, consolidate, and communicate strategic insights from country/regional teams to optimize clinical development...The Position Provides strategic leadership, functional expertise, and operational oversight for clinical trial...
of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g... your career in clinical research and lead challenging full-service projects on the country/regional levelwhile growing...
with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting... all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs...
of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g... your career in clinical research and lead challenging full-service projects on the country/regional levelwhile growing...
of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g... & experience - Significant experience in Clinical Research and site monitoring - Experience as a Study Manager or Leadwith...
with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting... all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs...
of projects in compliance with industry regulations, ICH-GCP, essential study documents, and applicable controlled documents (e.g... & experience - Significant experience in Clinical Research and site monitoring - Experience as a Study Manager or Leadwith...
with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting... all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs...
with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting... all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs...
, implementation, and management of projects in compliance with industry regulations, ICH-GCP, essential study documents... (if delegated by the Project Manager) - Prepares presentations and conducts training of Investigators - Ensures team compliance...