This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials objectives Working with a designated Data scientist to ensure high data quality Monitor the progress of research Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application public health sector Experience managing a clinical trial Good data management skills Able to work well in
epidemiological, clinical, and basic science research and innovation It currently manages several clinical trials objectives Working with a designated Data scientist to ensure high data quality Monitor the progress of research Maintain study site documentation following Good Clinical Practice Assist with any outstanding ethics application public health sector Experience managing a clinical trial Good data management skills Able to work well in
through public health-focused epidemiological, clinical, and basic science research and innovation
engagement activities
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 attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the and senior study personnel as and when required Data Quality Assurance & Control Ensure all study of quality Oversee resolution of any CRF, QC, and data queries Oversee adequate and completeness of participant
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 attend the 1-year, 2-year, and 3-year face-to-face clinical visit Maintain logs to remind study staff of the and senior study personnel as and when required Data Quality Assurance & Control Ensure all study of quality Oversee resolution of any CRF, QC, and data queries Oversee adequate and completeness of participant
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 attend the 1-year, 2-year, and 3-year face-to-face clinical visit
Data Quality Assurance & Control
manage bibliographic data and related research materials