Aj PersonnelJohannesburg
Main purpose of the job: The main purpose of a data manager in a scientific research setting is to oversee
oversee the collection, organization, and storage of data generated from experiments, observations, or surveys
the quality, security, and accessibility of the data throughout the research project and beyond Location:
areas: Technical Data Management and Analytics: Developing and implementing data management plans to ensure
ensure data is collected, processed, and stored in compliance with ethical, legal, and regulatory requirements
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Aj PersonnelJohannesburg
Main purpose of the job: The main purpose of a data manager in a scientific research setting is to oversee
oversee the collection, organization, and storage of data generated from experiments, observations, or surveys
the quality, security, and accessibility of the data throughout the research project and beyond Location:
areas: Technical Data Management and Analytics: Developing and implementing data management plans to ensure
ensure data is collected, processed, and stored in compliance with ethical, legal, and regulatory requirements
share this job on whatsapp
Johannesburg
job:
- The main purpose of a data manager in a scientific research setting is to oversee
oversee the collection, organization, and storage of data generated from experiments, observations, or surveys
the quality, security, and accessibility of the data throughout the research project and beyond
nical Data Management and Analytics:
Johannesburg
hire a Petrochemical Laboratory Manager. This role involves managing a team of skilled technicians and
operations as per ISO9001 and the QMS
Manage and mentor a team of laboratory technicians and
in optimal working conditionDevelop and manage the laboratory budget, ensuring cost-effective
testing methodsStrong leadership and team management skillsExcellent problem-solving and
skillsProficiency in laboratory information management systems (LIMS) and other relevant software
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Johannesburg
R480KPA
documentation
Safety Equipment and PPE ManagementREQUIREMENTS
Hillbrow
job:
- To provide best practice data collection, clinical assessments, collection of specimens,
t participant data from medical notes and complete CRFs
- Maintain full clinical records for all
SOPs
- Prepare all relevant reports
- Capture data timeously and accurately
- Provide regular
accountability for tasks and demonstrate effective self-management
- Follow through to ensure that quality
Nursing experience in STI/HIV, research and or clinical trials
Professional
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Hillbrow
e the site is well prepared for external lab, clinical, social science, and community monitoring reviews
Assist
on findings for the site management teamSupport the Regulatory/Data team with periodic quality
neededAssess staff awareness and compliance to Good Clinical Practice (GCP), Protocol requirements, Standard
accountability for tasks and demonstrate effective self-managementFollow through to ensure that quality
1-2 years of relevant work experience within a clinical research environment in Quality Control and Quality
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Hillbrow
projections and planning
Review data to identify trends, data quality issues, and areas for impro
files and data entries (i.e., eCRF’s, CRF’s)Support the storage and archiving of data as per the
audits, site inspections, and similarSupport data clean-up activities resulting from assessmentsEnsure
cipate in regular planning sessions with line manager and/or technical specialistsCompile prescribed
assignments and duties as needed, delegated by the line manager and within the scope of practiceSupport
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Johannesburg
activities, including analysis and interpretation of data, to conduct research relevant to the discipline
tests
Interpret test results together with epidemiological dataInterpret test results associated with outbreak
and solving technical problemsProject managementLaboratory Administration:
and report quality control issues to Laboratory ManagerDemonstrate cost consciousness and assists
attempt to solve them and report to Laboratory ManagerRequired Minimum Education
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Manpowergroup SaSouth Africa
an appropriate PV, vigilance system, and Risk Management to ensure appropriate oversight for products
pro-active Benefit Risk Management throughout product life cycle translating global safety data to insights and
Medical Safety Responsibility & Benefit Risk Management: Establish Product knowledge with a focus on
of AE/PQC material, where needed. PV contract management: Support LSO/CSTL with the local Pharmacovigilance
Pharmacovigilance System Master File (PSMF) contributions and data, as needed, accurately and in a timely manner. Responsible
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