accurate mapping of clinical trial data into a harmonised database, support data acquisition processes senior staff in improving the data harmonisation platform from a clinical standpoint
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 events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator
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 events Prepare for and manage participant visits and data capturing in line with protocol and site SOPs Perform requirements. Quality control of patient files and data entries (i.e., eCRF's, CRF's) Attend Investigator
through public health-focused epidemiological, clinical and basic science research and innovation
Clinical study management
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study
produce detailed reports, present to clients, analyze data, and develop strategies to
improve quality
standards.
• Design and execute quality monitoring programs to evaluate customer interactions (calls
quality metrics and benchmarks.
• Analyze quality data to identify trends, patterns, and areas for improvement;
/>service quality and customer satisfaction.
• Monitor compliance with company policies, procedures, and
skills with the ability to interpret data, identify trends, and make data driven decisions.
• Excellent
marking client's products vs competitor offering and monitor industry developments for threats and opportunities to be imported into Africa, including vehicles clinics. Planning and implementation all passenger FBU
monthly one-on-one meetings with supervised staff to monitor performance and support
Design and implement environmental monitoring programs to gather data on air, water, soil, and biodiversity biodiversity. Analyse environmental data using advanced statistical and modeling tools to provide actionable