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
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
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study
epidemiological, clinical and basic science research and innovation It currently manages a number of clinical trials brings together leading academic researchers, clinical and public health leaders, non-governmental organisations Main purpose of the job: To join the sub-EFFECT clinical study site(s) team and manage day-to-day activities Rossmore NICD, Sandringham Key performance areas: Clinical study management Contribute to the development requirements Participate in regular meetings between the clinical teams and cover duties of the EFFECT trial study
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
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
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming management, control and monitor expenditures of the clinic, adhering to relevant finance and procurement policies of the programme Support the implementation of clinical guidelines at a site level through on-site mentoring administrative procedures associated with accurate clinical record keeping and reporting including patient and accessibility of essential medicine for the clinic; and compliant and effective safety, quality control
project PrEP staff to ensure compliance with good clinical/Pharmacy Practice and maintenance of high standards compliance with good pharmacy practises and Ideal clinic requirements Provide guidance on the correct prescribing relevant authorities Compare pharmacy data to the clinic data Compile and submit comprehensive monthly report their career Certification in Basic HIV and Good Clinical Practice Exposure to public or private pharmacy
project PrEP staff to ensure compliance with good clinical/Pharmacy Practice and maintenance of high standards compliance with good pharmacy practises and Ideal clinic requirements Provide guidance on the correct prescribing relevant authorities Compare pharmacy data to the clinic data Compile and submit comprehensive monthly report their career Certification in Basic HIV and Good Clinical Practice Exposure to public or private pharmacy