focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development coordinating all aspects of clinical research study activities and ensuring that clinical research projects are and pre-screening process Conduct study-specific training as required Oversee adequate study-specific files attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the being involved on the floor Identifying staff training needs and being involved with addressing these
focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development coordinating all aspects of clinical research study activities and ensuring that clinical research projects are and pre-screening process Conduct study-specific training as required Oversee adequate study-specific files attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the being involved on the floor Identifying staff training needs and being involved with addressing these
focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development coordinating all aspects of clinical research study activities and ensuring that clinical research projects are pre-screening process
li>To provide best practice, data collection, clinical assessments, and collection of specimens (cord study requirement other than blood samples, if applicable
Required
job: To provide best practice, data collection, clinical assessments, and collection of specimens (cord study requirement other than blood samples, if applicable Obtain vital signs and other special investigations accurately and in a timely manner Maintain full clinical records for all participants Maintain an adequate attending training and development sessions and relevant Perform tasks based on the protocol training provided document this training Required minimum education and training: Diploma in General Nursing (Midwifery)
job: To provide best practice, data collection, clinical assessments, and collection of specimens (cord study requirement other than blood samples, if applicable Obtain vital signs and other special investigations accurately and in a timely manner Maintain full clinical records for all participants Maintain an adequate attending training and development sessions and relevant Perform tasks based on the protocol training provided document this training Required minimum education and training: Diploma in General Nursing (Midwifery)
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials coordinate the Mycology division projects Staff training and supervision of field staff Planning of field documentation following Good Clinical Practice Assist with any outstanding ethics application amendments and respond coworker relationships Required minimum education and training: Master's or Honour's Degree in Public Health the public health sector Experience managing a clinical trial Good data management skills Able to work
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials coordinate the Mycology division projects Staff training and supervision of field staff Planning of field documentation following Good Clinical Practice Assist with any outstanding ethics application amendments and respond coworker relationships Required minimum education and training: Master's or Honour's Degree in Public Health the public health sector Experience managing a clinical trial Good data management skills Able to work
through public health-focused epidemiological, clinical, and basic science research and innovation
Required minimum education and training:
Regulatory Authorities (Country Specific where applicable), Medicines and Related Substances Control Act Council, ensuring timeous processing of regulatory applications. Key Job Outputs Manage work streams for- and submission of new product applications in South Africa and other applicable territories, including but other human medicines. Prepare the registration applications for submission to the regulatory authorities pertaining to the pharmaceutical industry. Internal training and mentoring of peers when required. Establish