... compliance with study protocols Ensure clinical trials are executed in compliance with ... of more than one major clinical trial Ability to assist in preparation of a clinical development plan, clinical trial design, protocol writing, and essential ...
... and in the future. Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to ...
... Regulations, ICH Guidelines and other global regulatory requirements governing clinical research. Global clinical trial oversight required Excellent verbal and ...
... years of relevant experience in clinical operations global clinical trials in various positions, including minimum ...
... Regulations, ICH Guidelines and other global regulatory requirements governing clinical research. Global clinical trial oversight required Excellent verbal and ...
... review of data from oncology clinical trials with working knowledge of oncology ... ability to apply oncology and clinical trial knowledge to the review of ...
... review of data from oncology clinical trials with working knowledge of oncology ... ability to apply oncology and clinical trial knowledge to the review of ...
... will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while performing trial related activities for assigned protocols. ...
... review of data from oncology clinical trials with working knowledge of oncology ... ability to apply oncology and clinical trial knowledge to the review of ...
... review of data from oncology clinical trials with working knowledge of oncology ... ability to apply oncology and clinical trial knowledge to the review of ...