Medforum Medi Clinic Jobs in South Africa
Scientific / QA
- Aj Personnel (4)
- Insphired Recruitment Solutions (2)
- Lancet Laboratories Ltd (2)
- Mayfly Agri Ltd (2)
- Zest Worx (2)
- Mna Recruitment (1)
- Staff Solutions (1)
- Permanent
Research Audiologist Pretoria
Insphired Recruitment Solutions
Pretoria
R350 000 – R450 000 Working in a clinical environment and interacting with both clinical and non-clinical and academic colleagues and organization of data (user studies) User and Clinical Studies: 60%. Conducting user and usability engineering engineering studies, RETSPL studies, and clinical validation studies. Managing all aspects of the research team with required documentation. Investigating clinical & regulatory requirements and providing feedback
share this job on whatsappResearch Audiologist R350 000 – R450 000
Insphired Recruitment SolutionsPretoria
R350 000 – R450 000 Working in a clinical environment and interacting with both clinical and non-clinical and academic colleagues and organization of data (user studies) User and Clinical Studies: 60%. Conducting user and usability engineering engineering studies, RETSPL studies, and clinical validation studies. Managing all aspects of the research team with required documentation. Investigating clinical & regulatory requirements and providing feedback
Quality Assurance Administrator Klerksdorp, South Africa
Aj PersonnelKlerksdorp
performance of clinical trial related duties in research studies in accordance with Good Clinical Practice To conduct Quality Control activities for the clinical trials and train the site personnel in the protocol Course (for clinical trials) Advantageous ABC of Quality Control Certificate and Good Clinical Practice control procedures in clinical trials At least 2 - 3 years' experience working in clinical trials Desirable processes are conducted in accordance with Good Clinical Practice guidelines and regulations Delegation
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 To conduct Quality Control activities for the clinical trials and train the site personnel in the protocol Course (for clinical trials) Advantageous ABC of Quality Control Certificate and Good Clinical Practice control procedures in clinical trials At least 2 - 3 years' experience working in clinical trials Desirable processes are conducted in accordance with Good Clinical Practice guidelines and regulations Delegation
Quality Assurance Administrator (wits Phru)
Klerksdorp
performance of clinical trial related duties in research studies in accordance with Good Clinical Practice solving
Head Of Medical Affairs Gauteng
Mna RecruitmentGauteng
dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.). Key Responsibilities: Ensure products. Identify investigators appropriate for clinical trials. Act as a conduit for unsolicited, investigator-initiated initiation, oversight and follow up of assigned clinical studies and medical projects initiated within therapeutic area of the company (e.g. post marketing clinical activities such as registry/database projects physicians (individually or in groups meetings, clinical sessions, RTDs etc.), where requested. Participate
Project Manager Hillbrow, South Africa
Aj PersonnelHillbrow
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
Project Managers (x2 Wits Rhi) From To (basic Plus Benefits) - Yearly
Aj PersonnelHillbrow
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol performance areas: Oversee all operations in the clinical trial to ensure protocol and GCP compliance Assist queries and missing data with Investigators and Clinical Trials Assistants Communicate with CRO, Sponsor minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
Veterinarian - New Zealand $100,000 To $130,000 Nzd
Zest WorxSouth Africa
$100,000 to $130,000 NZD requirements and company policies Large animal clinical records are forwarded to administration team as
Veterinarian New Zealand
Zest WorxSouth Africa
$100,000 to $130,000 NZD requirements and company policies Large animal clinical records are forwarded to administration team as
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