Junior Lab Analyst (6 Month contract) required for a reputable company based in East
ensure compliance with BRC standards
product life cycle translating global safety data to insights and actions tailoring to local specificities Work with LSO/CSTL to provide medical input and insights for aggregate reports while undertaking a local (PV and non-medicinal product safety) : Provide insights on compliance metrics to CSTL/LSO Support LSO/CSTL Pharmacovigilance System Master File (PSMF) contributions and data, as needed, accurately and in a timely manner. Responsible language(s) and English language required Good in data analysis and reporting Proficiency in global and
product life cycle translating global safety data to insights and actions tailoring to local specificities Work with LSO/CSTL to provide medical input and insights for aggregate reports while undertaking a local (PV and non-medicinal product safety) : Provide insights on compliance metrics to CSTL/LSO Support LSO/CSTL Pharmacovigilance System Master File (PSMF) contributions and data, as needed, accurately and in a timely manner. Responsible language(s) and English language required Good in data analysis and reporting Proficiency in global and
study participants, conducting requisite sample and data collection as per protocol and Standard Operating effective, ethical participant engagement (must have insight into pregnancy, ante-natal care, and related challenges documentation/questionnaires and checklists
study participants, conducting requisite sample and data collection as per protocol and Standard Operating effective, ethical participant engagement (must have insight into pregnancy, ante-natal care, and related challenges documentation/questionnaires and checklists Ensure the data collected is complete and free from errors through abnormality in data collection to Study Coordinators or Medical Officers Collect required data from participant recruited daily in the study electronic database Address data queries and resolve them accordingly Any other duties
study participants, conducting requisite sample and data collection as per protocol and Standard Operating effective, ethical participant engagement (must have insight into pregnancy, ante-natal care, and related challenges documentation/questionnaires and checklists Ensure the data collected is complete and free from errors through abnormality in data collection to Study Coordinators or Medical Officers Collect required data from participant recruited daily in the study electronic database Address data queries and resolve them accordingly Any other duties
continuous improvement initiatives, leveraging insights from project execution to optimize processes, that should you upload personal information and data, that information will be shared with our
will be responsible for participant recruitment and data collection at the allocated study sites
will be responsible for participant recruitment and data collection at the allocated study sites
will be responsible for participant recruitment and data collection at the allocated study sites