Reference: NFU011858-ZAL-1 Embark on a pivotal role as a Corporate Analyst within a progressive organization. Job & Company Description: Your expertise in financial analysis and modelling will drive strategic financial decisions. Embark on a pivotal role as a Corporate Analyst within a progressi
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming populations in the Johannesburg Health District
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming populations in the Johannesburg Health District Monitor and review the implementation and progress of site Wits RHI Key Populations Programme team Regularly monitor and track site performance in relation to programme with senior management, control and monitor expenditures of the clinic, adhering to relevant finance and policies, contracts, and agreements Support the monitoring, evaluation & recording of outputs to evaluate
design, implementation and continuous improvement of clinic- and community[1]based primary, HIV, and gender-affirming populations in the Johannesburg Health District Monitor and review the implementation and progress of site Wits RHI Key Populations Programme team Regularly monitor and track site performance in relation to programme with senior management, control and monitor expenditures of the clinic, adhering to relevant finance and policies, contracts, and agreements Support the monitoring, evaluation & recording of outputs to evaluate
responsible for coordinating all clinical trial activities according to good clinical practice, the study protocol areas:
Desirable
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 key meetings to manage the study Manage site monitoring visits/audits or similar Manage procurement for 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 key meetings to manage the study Manage site monitoring visits/audits or similar Manage procurement for minimum work experience: 3-5 years experience in clinical trials/research Desirable additional education
and growth of relevant recognised Voluntary Associations, Licenced Bodies, and Service Providers Develop Registration, Renewal and the Recognition of Voluntary Associations (sections 18, 19, 22 and 25 of the Engineering Standard; Recognition Framework for Voluntary Associations); Provide inputs to the review of the legislative the natural growth of the database; Continually monitor and update the risk register as it pertains to the management of external/ forensic audit RFIs; Monitor the implementation of operational plans, manage
maintaining adequate budgets, which include costs associated with operations. Update and maintain the full audits Strong Costing Accounting Assigns tasks and monitors expectations Planning and prioritizing to meet
on a 12-month contract. Key Responsibilities: Monitor Accounts Receivable : Regularly review outstanding discrepancies. Credit Limit Management : Set and monitor credit limits for customers. Reporting : Prepare Risk Management : Identify and mitigate risks associated with credit and collections. Requirements: Experience