will be responsible for the following: Provide clinical oversight, timely medical advice and ensure implementation including specialized collections. Ensure SANBS donor clinic compliance to relevant legislation including the maintain and protect the health of blood donors. 2.7. Clinical decision making where deviations from protocols events by: 3.5.1 Providing clinical advice to attending staff on the optimal clinical management of such donors by: 3.6.1 Providing clinical advice to attending doctors on the optimal clinical management of such patients
will be responsible for the following: Provide clinical oversight, timely medical advice and ensure implementation including specialized collections. Ensure SANBS donor clinic compliance to relevant legislation including the maintain and protect the health of blood donors. 2.7. Clinical decision making where deviations from protocols events by: 3.5.1 Providing clinical advice to attending staff on the optimal clinical management of such donors by: 3.6.1 Providing clinical advice to attending doctors on the optimal clinical management of such patients
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
purpose of this position: The Case Manager utilising clinical knowledge and expertise, mitigates financial risk Responsibilities: Responsible for application of clinical knowledge in justifying patient hospitalisation hospitalisation Ensure accurate, specific and comprehensive clinical coding Timeous, effective communication and follow-up
purpose of the job: To provide clinical expertise in support of clinical research activities, including according to the study protocol and providing clinical insight and support to the local investigator quality assurance of study file source data, i.e. clinical source notes and CRFs to ensure the forms are study Accurately abstract information from the clinical notes Make sure that all the NHLS results have Professional Nurse Advantageous: REDCap Training Good Clinical Practice Certificate (GCP) Any qualification in