qualification. OOS investigation and documentation experience. Author Environmental monitoring reports and the lab as needed. Perform special studies when required. Lift and carry laboratory equipment and material Lab Training accountability and responsibility Head of department/ line manager: Accountable for ensuring you are trained Highlight additional training requirements to Line Manager where necessary DELEGATED RESPONSIBILITY: has no delegated responsibilities. This position requires the responsibility of delegation from reporting
qualification. OOS investigation and documentation experience. Author Environmental monitoring reports and the lab as needed. Perform special studies when required. Lift and carry laboratory equipment and material Lab Training accountability and responsibility Head of department/ line manager: Accountable for ensuring you are trained Highlight additional training requirements to Line Manager where necessary DELEGATED RESPONSIBILITY: has no delegated responsibilities. This position requires the responsibility of delegation from reporting
site regulatory and essential documents to all required stakeholders: Ethics Committees, South African regulatory bodies Ensure compliance with regulatory requirements within research studies Location: ILTBRU, Jose train the site personnel in the protocol and its requirements Review and Assess Case Report Forms, Informed protocol is adhered to at all times Ensure all required protocol parameters are followed and recorded notifications occur Provide expert guidance on the requirements of local and international regulatory bodies
site regulatory and essential documents to all required stakeholders: Ethics Committees, South African regulatory bodies Ensure compliance with regulatory requirements within research studies Location: ILTBRU, Jose train the site personnel in the protocol and its requirements Review and Assess Case Report Forms, Informed protocol is adhered to at all times Ensure all required protocol parameters are followed and recorded notifications occur Provide expert guidance on the requirements of local and international regulatory bodies
site regulatory and essential documents to all required stakeholders: Ethics Committees, South African bodies
requirements
study-specific pre-screening or screening (randomization if required) Provide background information about the study and when required (i.e. participant reimbursements) Document team meetings as and when required Compile activities, progress, etc. Take ownership and accountability for tasks and demonstrate effective self-management club, seminars, writing series workshops, etc. Required minimum education and training: Honors Degree Valid driver's license Required minimum work experience: 4 years of working experience in a research (qualitative
study-specific pre-screening or screening (randomization if required) Provide background information about the study and when required (i.e. participant reimbursements) Document team meetings as and when required Compile activities, progress, etc. Take ownership and accountability for tasks and demonstrate effective self-management club, seminars, writing series workshops, etc. Required minimum education and training: Honors Degree Valid driver's license Required minimum work experience: 4 years of working experience in a research (qualitative
study-specific pre-screening or screening (randomization if required)
Required minimum education and training:
< ong>Required minimum work experience:need one full year of RA Officer / RA Associate experience within the regulatory affairs department at a with SAHPRA, etc. The position requires a candidate with practical experience as a Regulatory Affairs Scientist as well as the current guidelines and requirements is required. Candidates must be able to work independently least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company to apply. Matric/
need one full year of RA Officer / RA Associate experience within the regulatory affairs department at a with SAHPRA, etc. The position requires a candidate with practical experience as a Regulatory Affairs Scientist as well as the current guidelines and requirements is required. Candidates must be able to work independently least one full year of RA Officer / RA Associate experience at a PHARMACEUTICAL company to apply. Matric/