Clinical Programme Specialist Jobs in Hillbrow
Programme Manager (key Populations Programme Wits Rhi)
Hillbrow
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming Populations Programme team
share this job on whatsappProgramme Manager Hillbrow, South Africa
Aj PersonnelHillbrow
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming Populations Programme team Regularly monitor and track site performance in relation to programme targets Actively participate in the Key Populations Programme's senior management team, providing support to management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies evaluate the impact of the programme Support the implementation of clinical guidelines at a site level
Programme Manager (key Populations Programme Wits Rhi) From To (basic Plus Benefits) - Yearly
Aj PersonnelHillbrow
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming Populations Programme team Regularly monitor and track site performance in relation to programme targets Actively participate in the Key Populations Programme's senior management team, providing support to management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies evaluate the impact of the programme Support the implementation of clinical guidelines at a site level
Project Managers (x2 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
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
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