Clinical Research and Development Specialist: HBM Ref: CRS/BM/LM Salary: Market related Location: Pretoria testing and roll -outs. Provide clinical research on an adhoc clinical topics. Providing feedback to Medical Hospital Benefit Management teams. Key requirements: Clinical Diploma or Degree (required) Active registration managed healthcare experience Minimum 5 years clinical experience as a nursing practitioner or pharmacist
us to change the health care system using your clinical knowledge and organisational skills. You must precisely, iterate, be lean, and prove yourself. Your clinical knowledge must be sound. You must be able to challenge admin staff) Assistance in the documentation of clinical information Maintain relationships between external improvement. Clinical process development: Understanding clinical process and engage with clinical data to understand the issues Provide clinical input into broad range of clinical developmental work including
us to change the health care system using your clinical knowledge and organisational skills. You must precisely, iterate, be lean, and prove yourself. Your clinical knowledge must be sound. You must be able to challenge admin staff) Assistance in the documentation of clinical information Maintain relationships between external improvement. Clinical process development: Understanding clinical process and engage with clinical data to understand the issues Provide clinical input into broad range of clinical developmental work including
qualification and/or Case Management qualification Diverse clinical nursing experience Case Management experience 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
HPCSA registered Medical Technologist (Clinical Pathology), who will be responsible for in the diagnosis, treatment, and monitoring of clinical conditions. Reporting to the Laboratory Manager discipline platforms as well as reviewing and verifying clinical results
dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.). Establish and maintain professional professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate. Screen relevant relevant training materials. Design and implement clinical research projects within defined standards and and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate
dossiers, HEOR dossiers, medical information packs, clinical expert reviews etc.). Establish and maintain professional professionals individually or in groups (meetings, clinical sessions, etc.), where appropriate. Screen relevant relevant training materials. Design and implement clinical research projects within defined standards and and budgets (e.g. Phase IV, post marketing clinical activities such as registry/database projects, epidemiological Support the affiliate Clinical Research Department in the management of clinical studies, as appropriate
integrating the clinical care and self-management aspects He/ She will be an integral part of the clinical and disease epidemiology, clinical management, conditions, and self-management of chronic conditions into clinical practice Participates in meetings and gives assistance to clinical, disease management and member counselor team of 3 years' experience in Disease Management, clinical patient management and health education within
emphasis on small stock/flock health management ); Clinical and herd/flock health services through the Onderstepoort Hospital, surrounding community and satellite clinics, including participation in a 24-hour service; reasonable time; A minimum of three years of veterinary clinical experience predominantly in Ruminant medicine specialist; Minimum of five years of veterinary clinical experience with at least three years' experience Veterinarian; Minimum of five years of veterinary clinical experience with at least three years' experience
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