Media Studies And Communication Jobs in South Africa
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Scientific / QA
- Mayfly Agri Ltd (8)
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- Permanent
Research Audiologist Pretoria
Insphired Recruitment Solutions
Pretoria
R350 000 – R450 000 (user studies) User and Clinical Studies: 60%. Conducting user and usability engineering studies, RETSPL RETSPL studies, and clinical validation studies. Managing all aspects of the research study. Develop research executing, and analysing surveys. Documenting and communicating user research findings. Preparing reports and Planning, conducting, and writing up of claims studies. Documentation: 25%. Assisting the Legal & and processes relevant. M. Communication Pathology in Audiology (or studying towards) 2 years of industry
share this job on whatsappResearch Audiologist R350 000 – R450 000
Insphired Recruitment SolutionsPretoria
R350 000 – R450 000 (user studies) User and Clinical Studies: 60%. Conducting user and usability engineering studies, RETSPL RETSPL studies, and clinical validation studies. Managing all aspects of the research study. Develop research executing, and analysing surveys. Documenting and communicating user research findings. Preparing reports and Planning, conducting, and writing up of claims studies. Documentation: 25%. Assisting the Legal & and processes relevant. M. Communication Pathology in Audiology (or studying towards) 2 years of industry
Junior Technologist
FreerecruitSouth Africa
sample reception where and if necessary. o Communication and liaison with clients pertaining to sample 17025. o Preparation of buffers, reagents, and media necessary for sample processing in compliance with plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) plating of samples; evaluation of microbial growth on media; isolation and identification of suspect isolates) self by attending courses and doing literature studies. o Improve knowledge about specific protocols,
Project Manager Hillbrow, South Africa
Aj PersonnelHillbrow
Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory authorities
Project Managers (x2 Wits Rhi) From To (basic Plus Benefits) - Yearly
Aj PersonnelHillbrow
Description Main purpose of the job: The project manager/study coordinator is responsible for coordinating all activities according to good clinical practice, the study protocol, and the site's standard operating procedures protocol and GCP compliance Assist study team with efficient study start-up, conduct, and close-out Manage Manage regulatory updates throughout the study (New ICFs, Protocol Amendments, etc.) Proactively resolve Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor, and regulatory authorities
Quality Assurance Administrator Klerksdorp, South Africa
Aj PersonnelKlerksdorp
performance of clinical trial related duties in research studies in accordance with Good Clinical Practice (GCP) Maintain a positive and constructive partnership with study Investigators and other site staff through constructive and its requirements Assist with regulatory communications, adherence, and regulatory file review Ensure appropriately and in a timely manner Discuss QC trends with study team during team meetings To pay particular attention and recorded accurately Ensure study staff is always following study standard operating procedures Required
Quality Assurance Administrator (wits Phru) From To (basic Plus Benefits) - Yearly
Aj PersonnelKlerksdorp
performance of clinical trial related duties in research studies in accordance with Good Clinical Practice (GCP) Maintain a positive and constructive partnership with study Investigators and other site staff through constructive and its requirements Assist with regulatory communications, adherence, and regulatory file review Ensure appropriately and in a timely manner Discuss QC trends with study team during team meetings To pay particular attention and recorded accurately Ensure study staff is always following study standard operating procedures Required
Quality Assurance Administrator (wits Phru)
Klerksdorp
performance of clinical trial related duties in research studies in accordance with Good Clinical Practice (GCP) n a positive and constructive partnership with study Investigators and other site staff through constructive requirements
Environmental Scientist Johannesburg
Michael PageJohannesburg
Scientist: Conduct environmental assessments and impact studies to evaluate the effects of projects and activities applying best practices to ongoing projects. Communicate research findings to both technical and non-technical conducting environmental assessments and impact studies. Strong analytically skills, with experience using and environmental modeling tools. Excellent communication and presentation skills. Ability to work collaboratively
Environmental Scientist
Michael PageJohannesburg
Scientist: Conduct environmental assessments and impact studies to evaluate the effects of projects and activities applying best practices to ongoing projects. Communicate research findings to both technical and non-technical conducting environmental assessments and impact studies. Strong analytically skills, with experience using and environmental modeling tools. Excellent communication and presentation skills. Ability to work collaboratively
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