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
Unit) has for over 20 years conducted numerous studies to assess the burden of and prevent vaccine-preventable vaccine-preventable diseases (VPD). Current studies and projects include infant rotavirus and BCG trials. Description operations manager to drive effective transversal business and facilities operations support With a multi-dimensional approach to problem-solving, risk management, and business continuity The operations team supports hard and Wits Health Consortium Shared Services Centre on business administration The incumbent will be someone with
Unit) has for over 20 years conducted numerous studies to assess the burden of and prevent vaccine-preventable vaccine-preventable diseases (VPD). Current studies and projects include infant rotavirus and BCG trials. Description operations manager to drive effective transversal business and facilities operations support With a multi-dimensional approach to problem-solving, risk management, and business continuity The operations team supports hard and Wits Health Consortium Shared Services Centre on business administration The incumbent will be someone with
performance areas: Inform participants about the study Screen potential participants and obtain informed informed consent according to SOPs Administer study questionnaires/interviews Draw blood/collect biological the fieldwork team if required Develop and update study-specific job aides Collect participant data from and other study documents Safekeeping of project assets Facilitate training of staff on study protocol timeously and accurately Provide regular updates on the study to key stakeholders Take ownership and accountability
performance areas: Inform participants about the study Screen potential participants and obtain informed informed consent according to SOPs Administer study questionnaires/interviews Draw blood/collect biological the fieldwork team if required Develop and update study-specific job aides Collect participant data from and other study documents Safekeeping of project assets Facilitate training of staff on study protocol timeously and accurately Provide regular updates on the study to key stakeholders Take ownership and accountability
participants following the study eligibility criteria Book and/or perform study-specific pre-screening or required) Provide background information about the study to participants prior to informed concern being each participant before conducting any qualitative study-related activities Conduct successful in-depth interviews in the development of qualitative SOPs and other study tools Assist with staff training as needed Develop qualitative analysis, writing, and dissemination of study results to participants and stakeholders Participation
participants following the study eligibility criteria Book and/or perform study-specific pre-screening or required) Provide background information about the study to participants prior to informed concern being each participant before conducting any qualitative study-related activities Conduct successful in-depth interviews in the development of qualitative SOPs and other study tools Assist with staff training as needed Develop qualitative analysis, writing, and dissemination of study results to participants and stakeholders Participation
QC activities are performed effectively across studies where trends are identified, coordinate relevant across all studies Assist with the review and revision of standard operating procedures per study-specific detailed knowledge, and understanding of the relevant studies and SOPs, knowledge of clinical research documentation
QC activities are performed effectively across studies where trends are identified, coordinate relevant across all studies Assist with the review and revision of standard operating procedures per study-specific detailed knowledge, and understanding of the relevant studies and SOPs, knowledge of clinical research documentation