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 resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Communicate with Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform Events of Medical Importance as per protocol requirements. Quality control of patient files and data entries
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 resolve protocol queries and missing data with Investigators and Clinical Trials Assistants Communicate with Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform Events of Medical Importance as per protocol requirements. Quality control of patient files and data entries
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming expenditures of the clinic, adhering to relevant finance and procurement policies Analyse data to track progress of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming expenditures of the clinic, adhering to relevant finance and procurement policies Analyse data to track progress of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming expenditures of the clinic, adhering to relevant finance and procurement policies