Description Main purpose of the job: Support research studies for optimal implementation Location: 22 Esselen Johannesburg Key performance areas: Support the study team with any research-related activity Support prescribed reports for timely submission to the study coordinator/leadership team Assist in patient recruitment experience, and personal abilities: Research Internships and/or exposure to clinical trial working environment
Description Main purpose of the job: Support research studies for optimal implementation Location: 22 Esselen Johannesburg Key performance areas: Support the study team with any research-related activity Support prescribed reports for timely submission to the study coordinator/leadership team Assist in patient recruitment experience, and personal abilities: Research Internships and/or exposure to clinical trial working environment
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
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
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
in accordance with requirements for the specific study After packing one kit will be Quality Controlled be quality control checking before dispatch to study sites Log dispatched kits onto the laboratory information a detailed list of bar codes of kit orders per study for reporting and statistical purposes Keep the
in accordance with requirements for the specific study After packing one kit will be Quality Controlled be quality control checking before dispatch to study sites Log dispatched kits onto the laboratory information a detailed list of bar codes of kit orders per study for reporting and statistical purposes Keep the