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Data Coordinator / Data-koördineerder wanted immediately: APPLY HERE

Data Coordinator / Data-koördineerder wanted immediately: APPLY HERE

Bellville, Western Cape

Bestuur die insameling, bewaring en lewering van hoë kwaliteit data vir die volle duur van elke navorsingsprojek:
Lewer insette in die ontwerp van databasisse en -insamelingsinstrumente om sodoende te verseker dat dit voldoen aan die vereistes vir vaslegging van en verslagdoening oor
kliniese data van wisselende kompleksiteit;
Toets projekdatabasisse en -vasleggingskerms om te verseker dat dit aan die protokol voldoen, sowel as aan institusionele prosesse en prosedures;
Beproef nuwe prosesse en sisteme ten einde die data uit kliniese navorsing optimaal te bestuur;
Verwerk data, spoor dit na en valideer dit akkuraat en betyds, ooreenkomstig die voorskrifte vir dataverwerking en -vaslegging;
Bestuur die protokol rakende pasiëntinligting en oorsig, en betrek protokolspesifieke riglyne by die dataoorsigproses;
Aanvaar die primêre verantwoordelikheid vir datagehalte deur met die datavaslegging- en die datagehaltespan te skakel, asook met projekleiers;
Verrig protokolspesifieke gehaltekontrole- en gehalteversekeringstake onafhanklik vir elke projek;
Verseker dat goeie kliniese praktyk en goeie kliniese-data-bestuurspraktyk nagevolg word, asook standaardprosedures en werksvoorskrifte;
Ontwikkel en onttrek akkurate dataverslae soos nodig vir voortgesette projekdeurvoering en vir disseminasie;
Onttrek en analiseer verslae soos en wanneer nodig;
Aankoop van IT-toerusting, soos en wanneer nodig;
IT-kennis om te help met tegniese IT-probleme;
Werkende kennis van IT-programmering.

Managing the collection, maintenance and delivery of high-quality data throughout the duration of every research project;
Contributing to the design of databases and data collection tools, ensuring that they meet the requirements for entering and reporting clinical data of varying complexity;
Testing project databases and data entry screens to assure compliance with the protocol and institutional processes and procedures;
Testing new processes and systems for the optimal management of data in clinical research;
Processing, tracking and validating data accurately and on time, in accordance with the instructions for data processing and entering;
Managing the patient information and review protocol, and incorporating protocol-specific guidelines into the data reviewing process;
Taking the primary responsibility for data quality, liaising to that purpose with the teams for data entry and data quality, as well as with project leaders;
Performing project-specific quality control and quality assurance tasks for each project independently;
Ensuring adherence to good clinical practice, good clinical data management practices, and to standard procedures and working instructions;
Developing and extracting accurate data reports as needed for ongoing project implementation and for dissemination;
Extracting and analysing reports as and when required;
Purchasing of IT equipment, as and when required;
Sound IT knowledge to assist with technical IT issues;
Sound working knowledge of IT programming.

Minstens vyf jaar ervaring van databestuur, verkieslik in ‘n Mediese/ Kliniese navorsingsomgewing;
Ervaring met kliniese-data-bestuurstelsels (bv. REDCap);
Uitstekende praktiese kennis van verskeie sagtewarepakkette vir databasisbestuur (bv. SQL Server 2005/2008 en MS Access);
‘n Uitstekende vermoë om navrae te formuleer: T-SQL, ETL (ekstraheer, transformeer, laai);
Die vermoë om ‘n groot hoeveelheid data akkuraat en doeltreffend te hanteer;
Bereidwilligheid om skiktyd te werk
Die vermoë om in spanverband te werk en aktief tot vaardigheidsoordrag by te dra;
Die vermoë om dataverwante bedrywighede deeglik en konsekwent aan te teken;
Die vermoë om sistematies te werk te gaan en om verskillende inligtingsbronne en -stelsels byeen te bring;
Die vermoë om vertroulike inligting professioneel te hanteer;
Goeie skriftelike en mondelinge kommunikasievaardighede.

At least five years’ experience of data management, preferably in a research environment;
Experience with clinical data management systems (e.g. REDCap)
Excellent working knowledge of various database management software packages (e.g. SQL Server 2005/2008 and MS Access);
Excellent query writing skills: T-SQL, ETL (extract, transform, load);
The ability to deal with large volumes of data accurately and efficiently;
The willingness to work flexitime;
The ability to work collaboratively in a team and to actively engage in skills transfer;
The ability to document data-related activities well and consistently;
The ability to work systematically and to integrate various sources of information and systems;
The ability to handle confidential information in a professional manner;
Good verbal and written communication skills.

N/A

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Source: Indeed

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