Data Manager/statistician

University of Antwerp
Antwerpen, Belgium
1 day ago
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Role details

Contract type
Temporary contract
Employment type
Full-time (> 32 hours)
Compensation
€14,768.0 - €18,928.0
Working hours
Regular working hours
Languages
Dutch, English, French
Job source

Tech stack

Data Analysis Big Data Spreadsheets Clinical Data Repository Databases Computer Literacy Data Validation Data Integrity Electronic Data Capture R (Programming Language) Python (Programming Language) Meta-Data Management
+4 more
Microsoft Office SAS (Software) Data Storage Technologies Data Management

Job description

  • Development of databases and data specifications, including design, user requirements and access rights, building in controls, validating data;
  • Development and maintenance of all data management documentation (SOP, work instructions, study-specific data management documents);
  • Perform quality assurance/quality control-checks of data captured in the clinical database, in line with company quality standards and coordinate timely database corrections with clinical sites;
  • Maintain databases throughout their life cycle to ensure data integrity, generate and review documentation regarding database changes;
  • Reviewing clinical data;
  • Monitor and track data entry and resolve queries according to agreed timelines;
  • Assist in monitoring study statistics and site performance;
  • Assist in standardising procedures around meta-data management;
  • Coordinate archiving of study databases and related documents (including backup, optimisation, integrity verification);
  • Assist in the procurement of software, hardware and data storage upgrades;
  • Be willing to make regular field visits to DR Congo (and possibly other African countries) to oversee data management or related activities and install necessary software;
  • Provide training on data management to the study teams (in Belgium and international institutions);
  • Assume responsibility for leading, supervising and monitoring the data management activities of the clinical research organisation (CRO);
  • Managing potential protocol violations/deviations within clinical studies;
  • Perform sample size calculations;
  • Analysing collected data in R or SAS, You will report to and be supervised by the PregInPoxVac or Tumaini Senior Data Manager and Project Manager, who have a direct functional link with the Principal Investigators of these clinical trial.

Requirements

  • Minimum master’s degree in Epidemiology, Statistics, or a related field;
  • Good understanding of clinical studies and knowledge of or training in ICH Good Clinical Practices;
  • High proficiency with MS Office;
  • Experience in Electronic Data Capture systems (e.g. RedCap, Medrio, etc.);
  • Computer experience in database, spreadsheet and analysis software (e.g. R, SAS, Python);
  • Knowledge of basic medical terminology is required, as well as scientific and clinical research methods;
  • Knowledge of and experience with industry standards related to data management, i.e. CDISC, SDTM, ADaM, is a plus;
  • Ability to work with large data sets with attention to detail;
  • Ability to apply knowledge and skills effectively in a highly organised manner, adhering to legal guidelines and standard operating procedures;
  • Excellent organisational skills and good analytical / problem-solving skills;
  • Strong interest in scientific work, flexible attitude and strong sense of initiative and responsibility;
  • Good communication skills;
  • Excellent knowledge of English, good knowledge of French; knowledge of Dutch is a plus;
  • Ability to work in a team and if necessary independently, to (train) the study team, in Belgium and in Africa;
  • Ability to work productively with minimal supervision and meet deadlines;
  • Willing to travel to (remote) sites in Africa;
  • Experience working with/in developing countries (preferably in Africa) is a great asset;
  • Experience as a (clinical) data manager and data analysis is an asset.

Benefits & conditions

  • Meal vouchers
  • Internet cost / Subscription
  • Additional paid leave
  • Parking
  • Public transport contribution
  • Eco Cheque
  • Training
  • Remote work

  • Working in an intellectually stimulating, international and interdisciplinary research environment, with room for personal initiative;
  • A fixed-term contract of 12 months for 1 FTE position, with perspective of extension for at least another 2 years;
  • Start date: October or November 2026;
  • You will receive a gross monthly salary within pay band 7.1-9.1 of the pay scales of the Administrative and Technical Staff. Your entry-level grade depends on your relevant professional experience. More information on our pay scales and other benefits can be found here on our website.
  • You get meal vouchers, eco vouchers, internet connectivity allowance, group insurance, guaranteed income insurance, and a bicycle allowance or full reimbursement of your commute by public transport;
  • You will work largely at Campus Drie Eiken with in a dynamic and stimulating working environment and flexible working time arrangements.

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