stakeholder inputs – e.g., ensure that Wits RHI is represented in all field verification site visits Ensure other stakeholders and ensure that Wits RHI is represented Ensure optimal communication between and across other information regarding the position. We offer Medical Aid Contribution, Provident Fund Contribution
Client's products. This role will support the medical components of Pharmacovigilance (PV) for the Company provide guidance on productive cross-functional medical safety collaborations for the Company and Clients Supporting the Business/ Commercial team in PV medical aspects in the development of contracts and proposals attending BID defence meetings and conferences as the medical expert, as required. Providing Senior Management specific project/ Client activities. Developing PV medical raining presentations and delivering training,
Client's products. This role will support the medical components of Pharmacovigilance (PV) for the Company provide guidance on productive cross-functional medical safety collaborations for the Company and Clients Supporting the Business/ Commercial team in PV medical aspects in the development of contracts and proposals attending BID defence meetings and conferences as the medical expert, as required. Providing Senior Management specific project/ Client activities. Developing PV medical raining presentations and delivering training,
declared medically fit for the position and environment, as determined by a risk-based medical examination briefing and task activity sessions to represent area of accountability and act as a conduit for
requirements and related standards / guidelines Relevant medical degree or science degree 5 years of documented biostatistics included Experience and application of medical device regulations (MDR 2017/745; 21CFR820; Act documents and standards (ISO 14155) Experience in medical writing, conducting systematic review and clinical
requirements and related standards / guidelines Relevant medical degree or science degree 5 years of documented biostatistics included Experience and application of medical device regulations (MDR 2017/745; 21CFR820; Act documents and standards (ISO 14155) Experience in medical writing, conducting systematic review and clinical
Post claim management and settlement. Medical bill reviewing. Medical case management. Complex problem identification
Post claim management and settlement. Medical bill reviewing. Medical case management. Complex problem identification
submission requirements. The company is positively represented to various stakeholders, constructive interactions communicated to the business. The company is positively represented to various stakeholders for constructive interactions provided. Constructive feedback from regulatory and medical colleagues on sharing of best practices. Personal
stakeholder inputs – e.g., ensure that Wits RHI is represented in all field verification site visits Ensure other stakeholders and ensure that Wits RHI is represented Ensure optimal communication between and across other information regarding the position. We offer Medical Aid Contribution, Provident Fund Contribution