Data Bioanalysis•Analysis and processing of analytical data accumulated during the method validation and analytical phases for various analytes and techniques,•Collation and analysis of raw and processed data at the end of each phase,•Compilation of method validation, bioanalytical and stability reports,•Responsibility for the acceptance of accuracy and integrity of data before the study documentation are submitted for auditing,•Conforming to the ISO (International Organization for Standardization) standard, GLP (Good Laboratory Practice) and GCP (Good Clinical Practice) principles, EMA (European Medical Agency), SANNAS (South African National Accreditation System).•Keeping pace with developments in analytical chemistry, immunochemistry and / or related fields specifically through published works (specifically white papers).•Writing and updating SOP (Standard Operating Procedures) as well as the various templates, forms and spreadsheets linked to these SOPsTechnical and scientific input required for the writing of reports.Assisting with Project Management activities as delegated by the Project Manager.Advising, assisting and training junior personnel in aspects related to the processing of data and writing of reports for studies.

Data Bioanalysis•Analysis and processing of analytical data accumulated during the method validation and analytical phases for various analytes and techniques,•Collation and analysis of raw and processed data at the end of each phase,•Compilation of method validation, bioanalytical and stability reports,•Responsibility for the acceptance of accuracy and integrity of data before the study documentation are submitted for auditing,•Conforming to the ISO (International Organization for Standardization) standard, GLP (Good Laboratory Practice) and GCP (Good Clinical Practice) principles, EMA (European Medical Agency), SANNAS (South African National Accreditation System).•Keeping pace with developments in analytical chemistry, immunochemistry and / or related fields specifically through published works (specifically white papers).•Writing and updating SOP (Standard Operating Procedures) as well as the various templates, forms and spreadsheets linked to these SOPs.

• The processing and quality control of bioanalytical data accumulated during the validation and production phases of BE and clinical studies studies and collation of processed data. • Interpretation of chromatography, key parameters, trends and results.• Conforming to the ISO/IEC 17025 standard, GLP principles and other quality systems and regulations that may be applicable.• Assisting with aspects related to information technology, systems validations and logistics management, which may reasonably be delegated by the Management of BASD.• Keeping pace with developments in analytical chemistry, immunochemistry and/or related fields which have a bearing on the optimal functioning of the group.• Complying with SOPs relevant to area of work.