ICH GCP. Meticulous attention to detail in patient data recording. Completion and management of study documentation clinical trial processes. Conduct clinical trials and provide medical oversight. Liaise with stakeholders and per protocol. Participate in and initiate trial data publications. Oversee regulatory processes, participant as per protocols. Conduct and attend relevant training. Review and action laboratory results. Interpret Interpret ECGs, CXRs, etc. Address monitoring and data queries. Review and draft SOPs. Prepare source documents
ICH GCP. Meticulous attention to detail in patient data recording. Completion and management of study documentation clinical trial processes. Conduct clinical trials and provide medical oversight. Liaise with stakeholders and per protocol. Participate in and initiate trial data publications. Oversee regulatory processes, participant as per protocols. Conduct and attend relevant training. Review and action laboratory results. Interpret Interpret ECGs, CXRs, etc. Address monitoring and data queries. Review and draft SOPs. Prepare source documents
that all stock and services related costs are captured for month end close off;
Closing
incidents and unsafe acts are reported. Provide on the job training. Assess and approve contractors Safety & Safety Reps functioning. Identification of training needs. Standby duties on rotational basis. Grade
policies and procedures.
Plant (Chrome and PGM recovery) experience.
- Training experience will be advantageous
- Computer
closing out reports
- Provide site induction and on the job training
- Assess contractor H&S
in the preparation of budgets and forecasts, providing valuable insights to support decision-making processes
a focus on new German HESS machinery. Training will be provided. Requirements: Advanced electrical skills
Safety Act policies and procedures. Provide coaching and on-the-job training to reporting staff. Communicate