LOM, MTP, STP, Scoping/Concept, PFS, BFS) Pit/Stope Optimisation Mine Design Mine Scheduling Equipment
LOM, MTP, STP, Scoping/Concept, PFS, BFS) Pit/Stope Optimisation Mine Design Mine Scheduling Equipment
For a confidential discussion please contact Lisa-Mari on (021) 035 1433 or send your CV to l.jordan(at)thetalentexperts
For a confidential discussion please contact Lisa-Mari on (021) 035 1433 or send your CV to l.jordan(at)thetalentexperts
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
This role will play a key role in bringing deep clinical understanding and judgment in benefit-risk assessments role will also ensure projects adhere to Good Clinical and Pharmacovigilance Practice and Regulatory interpretation of safety information collected from pre-clinical through to post-marketing, including medical review Investigator's Brochures, Clinical Study Protocol, Study Safety Plans, and Clinical Safety reports. Reviewing interpretation of safety information collected from pre-clinical through to post-marketing, including medical review
Provide clinical inputs on ex-gratia funding requests Open, review and resolve all clinical queries and and assessments through providing a clinical decision or requesting more information where required Implement authorisation and claiming is facilitated Provide clinical training / support to identified stakeholders Knowledge and application of clinical principles and processes Knowledge of clinical and funding protocol development development Clinical research and assessment Knowledge of scheme rules and contractual negotiations Skill:
Provide clinical inputs on ex-gratia funding requests Open, review and resolve all clinical queries and and assessments through providing a clinical decision or requesting more information where required Implement authorisation and claiming is facilitated Provide clinical training / support to identified stakeholders Knowledge and application of clinical principles and processes Knowledge of clinical and funding protocol development development Clinical research and assessment Knowledge of scheme rules and contractual negotiations Skill:
Requirements: Grade 12 / Matric Diploma in Clinical Engineering/ Electrical Engineering (light current current or higher) Minimum of 6 years relevant Clinical Engineering experience in a hospital environment Fully
SKILLS REQUIRED INCLUDE: Grade 12/Matric Diploma in Clinical Engineering/Electrical Engineering light current current or higher At least 6 years relevant Clinical Engineering experience in a hospital/medical equipment