Klínískur öryggisfulltrúi
Klínískir öryggisfulltrúar eru skráðir klínískir starfsmenn sem tryggja að heilbrigðisupplýsingakerfin sem stofnunin smíðar, kaupir og setur upp séu örugg fyrir sjúklinga. Þeir stýra ferli klínískrar áhættustýringar, leiða greiningu hættna, bera ábyrgð á hættuskrám og skrifa og samþykkja skýrslur um klínísk öryggismál, með stöðlum um klíníska áhættustýringu eins og ISO 14971 og IEC 80001-1.
Þessi texti var þýddur úr ensku af gervigreindaraðstoðarmanni og hefur ekki enn verið yfirfarinn af móðurmálshafa. Tilvitnanir í UK GDaD PCF (hæfniramma bresku ríkisstjórnarinnar fyrir stafræn störf og gagnastörf) og í ESCO haldast á ensku.
- Hlutverk í UK GDaD PCF
- Ekkert: þessi viðmiðun skilgreinir hlutverkið
- Starfsgreinar í ESCO
- clinical informatics manager (ISCO-08 1342); regulatory affairs manager (ISCO-08 2619)
- Á GitHub
- Hlutverkaskjal · Hlutverkagögn
Stig
| Launaflokkur | Hlutverkastig | Stig í UK GDaD PCF | Launaþrep bresku opinberu þjónustunnar | Stig starfsmats |
|---|---|---|---|---|
| 7 | Klínískur öryggisfulltrúi | — | — | 522 |
| 8a | Eldri klínískur öryggisfulltrúi | — | — | 577 |
| 8b | Yfirmaður klínísks öryggis | — | — | 619 |
Í stofnun á sviði stafrænnar heilbrigðis- og velferðarþjónustu
- Hlutverkið verður að vera í höndum skráðs klínísks starfsmanns, svo öryggismat byggi á núgildandi klínískri þekkingu og faglegri ábyrgðarskyldu.
- Heilbrigðisupplýsingatækni getur skaðað sjúklinga með röngum, vantandi, seinkuðum eða villandi upplýsingum, svo hlutverkið metur áhættu sem er oft falin í gögnum og vinnuflæði.
- Vinna við klínískt öryggi nær yfir allan líftíma kerfis, frá hönnun og innkaupum til útsetningar, breytinga og úreldingar.
- Sumar vörur eru einnig lögbundnar sem lækningatæki, svo hlutverkið vinnur með regluverks- og gæðasamstarfsfólki þar sem öryggismál og tækjaskrár skarast.
- Öryggisatvik tengd heilbrigðisupplýsingatækni geta valdið alvarlegum skaða, svo hlutverkið rannsakar atvik og tryggir að lærdómur sé dreginn.
Starfsgreinar og færni í ESCO
ESCO telur upp þá færni og þekkingu sem vinnuveitendur þurfa yfirleitt (nauðsynleg) eða geta þurft (valfrjáls) fyrir hverja starfsgrein. Notaðu þær sem gátlista fyrir samtöl um þróun.
clinical informatics manager
Clinical informatics managers oversee the daily operations of information systems used in a medical institutions. They also carry out research, using their understanding of clinical practices to find ways to improve healthcare services.
Nauðsynleg: færni og þekking (28)
Færni og hæfni
- adhere to organisational guidelines
- analyse large-scale data in healthcare
- apply good clinical practices
- apply organisational techniques
- collect healthcare user's general data
- communicate in healthcare
- comply with quality standards related to healthcare practice
- conduct clinical software research
- contribute to continuity of health care
- contribute to public health campaigns
- follow clinical guidelines
- oversee clinical information system activities
- perform clinical coding procedures
- review patient's medical data
- use clinical assessment techniques
- use foreign languages for health-related research
Þekking
Valfrjáls: færni og þekking (31)
Færni og hæfni
- advise on training courses
- communicate in foreign languages with health service providers
- comply with legislation related to health care
- implement strategic planning
- inform policy makers on health-related challenges
- manage budgets
- manage project metrics
- manage workflow processes
- meet deadlines
- participate in medical records' auditing activities
- perform project management
- recruit employees
- supervise staff
- train employees
Þekking
- IBM InfoSphere DataStage
- IBM InfoSphere Information Server
- Informatica PowerCenter
- Oracle Data Integrator
- Oracle Warehouse Builder
- Pentaho Data Integration
- QlikView Expressor
- SAP Data Services
- SQL Server Integration Services
- analytical methods in biomedical sciences
- audit techniques
- conditions for professional practice of clinical psychology
- creation of clinical psychological opinions
- data extraction, transformation and loading tools
- health psychology
- healthcare analytics
- manage healthcare staff
regulatory affairs manager
Regulatory affairs managers are in charge of regulatory and legal affairs in several sectors such as the healthcare, energy and banking industries. They oversee the development of products and services from inception to market release by making sure everything complies with the local legislation and meets regulatory requirements. They have experience in the different phases of regulatory processes and act as an interface between business and government legislation or regulatory boards.
Nauðsynleg: færni og þekking (26)
Færni og hæfni
- advise on efficiency improvements
- analyse legislation
- comply with legal regulations
- develop company strategies
- develop licensing agreements
- develop organisational policies
- enforce financial policies
- ensure compliance with company regulations
- ensure compliance with legal requirements
- ensure compliance with policies
- ensure products meet regulatory requirements
- identify legal requirements
- implement strategic planning
- integrate strategic foundation in daily performance
- interpret technical requirements
- manage relationships with stakeholders
- meet the requirements of legal bodies
- monitor company policy
- monitor compliance with licensing agreements
- organise business documents
- prepare licence agreements
Þekking
Valfrjáls: færni og þekking (25)
Færni og hæfni
- advise on legal decisions
- analyse legal enforceability
- analyse scientific data
- communicate with banking professionals
- contact scientists
- identify hazards in the workplace
- keep updated on innovations in various business fields
- protect personal data and privacy
- provide legal advice
- support managers
Þekking
- banking activities
- copyright legislation
- corporate law
- corporate social responsibility
- financial jurisdiction
- financial products
- hazard analysis and critical control points
- intellectual property law
- international trade
- law enforcement
- nuclear legislation
- patents
- procurement legislation
- quality standards
- tax legislation
Contains ESCO v1.2.1 data (https://esco.ec.europa.eu/). © European Union. Reuse authorised under Commission Decision 2011/833/EU.