Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve investigators regarding participant welfare while on study Notify relevant parties of Serious Adverse Events
Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve investigators regarding participant welfare while on study Notify relevant parties of Serious Adverse Events
sub-EFFECT clinical study site(s) team and manage day-to-day activities of the study site(s) To provide care to patients participating according to the study protocol Location: Chris Hani Baragwanath Academic performance areas: Clinical study management Contribute to the development of study documentation including EFFECT trial study team during staff leave period Maintain close contact with the study management group financial implications for the project Conduct clinical study in accordance with GCP regulations and standard
sub-EFFECT clinical study site(s) team and manage day-to-day activities of the study site(s) To provide care to patients participating according to the study protocol Location: Chris Hani Baragwanath Academic performance areas: Clinical study management Contribute to the development of study documentation including EFFECT trial study team during staff leave period Maintain close contact with the study management group financial implications for the project Conduct clinical study in accordance with GCP regulations and standard
performance of clinical trial related duties in research studies in accordance with Good Clinical Practice (GCP) Maintain a positive and constructive partnership with study Investigators and other site staff through constructive appropriately and in a timely manner Discuss QC trends with study team during team meetings To pay particular attention and recorded accurately Ensure study staff is always following study standard operating procedures Required
performance of clinical trial related duties in research studies in accordance with Good Clinical Practice (GCP) Maintain a positive and constructive partnership with study Investigators and other site staff through constructive appropriately and in a timely manner Discuss QC trends with study team during team meetings To pay particular attention and recorded accurately Ensure study staff is always following study standard operating procedures Required