Clinical Trail Researcher required for Institute in Cape Town. Clinical Trail Researcher required for
Clinical Trail Researcher required for Institute in Cape Town. Clinical Trail Researcher required for
thinking, planning and execution of initiatives to support the growth of AEON in line with institutional strategies Management (including the Office for Research Support and Management, Office for Institutional Strategy
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job manager and within the scope of practice Manage and support staff members Required minimum education and training:
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor procurement for the study Assist team members and support teams with an open helpful attitude, perform on-the-job manager and within the scope of practice Manage and support staff members Required minimum education and training:
CONTRACT
EMAVUNDLENI CLINICAL RESEARCH SITE; CROSSROADS
The Desmond carry out laboratory activities at Emavundleni Clinical Research Site, as well as to ensure that the final of health and safety regulations
Advantageous:
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews report/s on findings for the site management team Support the Regulatory/Data team with periodic quality Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality of the relevant studies and SOPs, knowledge of clinical research documentation Computer literate with
Ensure the site is well prepared for external lab, clinical, social science, and community monitoring reviews report/s on findings for the site management team Support the Regulatory/Data team with periodic quality Assess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard 1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality of the relevant studies and SOPs, knowledge of clinical research documentation Computer literate with
e the site is well prepared for external lab, clinical, social science, and community monitoring reviews
job: To provide best practice data collection, clinical assessments, collection of specimens, and care medical notes and complete CRFs Maintain full clinical records for all participants Maintain an inventory nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African similar will be an advantage Certification in good clinical practice Experience in a research environment