Clinical Facilitator Jobs in Johannesburg, Gauteng
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Last 7 days
Clinical Coder Randburg
Blue Marble Recruitment
Randburg
The Clinical Coder will play a critical role in ensuring accurate and timely coding of medical procedures Working closely with healthcare providers, the Clinical Coder will review patient records, assign appropriate preferred. Minimum of 2 years of experience in clinical coding within a healthcare setting. Proficiency
share this job on whatsappAesthetic Therapist Needed For Busy Aesthetic Clinic In Sandton
Sandton
7500 Monthly
Aesthetics Therapist needed in Sandton
- Diploma in Somatology/ Aesthetic / Health & Skincare qualification.
- MUST have CIDESCO/ ITEC/ or SAAHSP qualifications.
- MUST have Cruise ship experience
- At least 3 years of working experi
Medical Advisor Sunninghill
Universal HealthJohannesburg
setting. They provide medical expertise, review clinical policies and guidelines, and collaborate with outcomes while managing costs. Review and assess clinical policies, treatment guidelines, and utilization appropriateness, and cost-effectiveness. Provide clinical support and guidance to internal teams, including assess new and existing clinical policies and protocols from an evidence-based, clinical and financial impact input and clinical advisory services. Presentations will often be required. Provide clinical technical
Medical Advisor Market Related
Universal HealthJohannesburg
setting. They provide medical expertise, review clinical policies and guidelines, and collaborate with outcomes while managing costs. Review and assess clinical policies, treatment guidelines, and utilization appropriateness, and cost-effectiveness. Provide clinical support and guidance to internal teams, including assess new and existing clinical policies and protocols from an evidence-based, clinical and financial impact input and clinical advisory services. Presentations will often be required. Provide clinical technical
Research Nurse Hillbrow, South Africa
Aj PersonnelHillbrow
job: To provide best practice data collection, clinical assessments, collection of specimens, and care medical notes and complete CRFs Maintain full clinical records for all participants Maintain an inventory study documents Safekeeping of project assets Facilitate training of staff on study protocol and SOPs nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African similar will be an advantage Certification in good clinical practice Experience in a research environment
Research Nurses (x 2 Wits Rhi) From To (basic Plus Benefits) - Yearly
Aj PersonnelHillbrow
job: To provide best practice data collection, clinical assessments, collection of specimens, and care medical notes and complete CRFs Maintain full clinical records for all participants Maintain an inventory study documents Safekeeping of project assets Facilitate training of staff on study protocol and SOPs nursing experience in STI/HIV, research and or clinical trials Professional body registration: South African similar will be an advantage Certification in good clinical practice Experience in a research environment
Research Nurses (x 2 Wits Rhi)
Hillbrow
Professional
be an advantage
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 (x 3 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
Project Managers (x 3 Wits Rhi)
Hillbrow
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol 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
experience:
- 3-5 years experience in clinical trials/research
Desirable
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