Blank
Loslegen
Blank
Karrierechancen
Zurück zur Jobsuche

Junior Clinical Data Manager

Our client located in the Walloon Brabant is actively looking for a Junior Clinical Data Manager.

Hybrid working opportunity (min. 1 day/week on site at the client's location is required).

Job description

As a Clinical Data Manager, you provide support to the Clinical Data Management (CDM) team in managing specific data entry and data review tasks under the supervision of the Lead CDM responsible for the project. You provide support to the CDM programming team in executing Quality Control (QC) activities under the supervision of the CDM Programming Specialist and Lead Clinical Data Manager responsible for the projects. You provide information and advice for questions on the data entry, data review and quality control activities.

Responsibilities

  • You create annotated CRF
  • You perform Data Review activities:
    • Generate queries and review for consistency;
    • Perform data modifications according to query answers.
  • You perform the reconciliation of SAE and external vendor datasets (including resolution and follow-up of the inconsistencies).
  • You perform Quality Control (QC) activities:
    • Data entry of dummy data;
    • Test reports, listings and patient profiles to ensure that they work correctly based on the dummy data entered;
    • Report on findings and follow-up until resolution. (QC activities are done on: annotated CRFs, SAS reports and SAS listings, patient profiles, checks, dummy unblinded datasets, standard and SDTM tabulations, patient PDFs and data)
  • You perform Data Entry activities:
    • Registration, verification, tracking of CRFs and other forms in CDMS prior to data entry and management in accordance with priorities;
    • Data entry of CRFs and other forms; this also includes Laboratory Normal Ranges;
    • Correction of inconsistencies between two entries.
  • You provide support for the Coding activities: upload terms in ID-Code, communication with coders and medical reviewers, provide coding status and check out pending terms.
  • You perform EDC data extracts (snapshots) either on pre-defined frequencies or upon request.
  • You file CRF pages. Send the patient PDF files either to the sponsor or investigator sites.
  • You perform tasks in accordance with the company Standard Operating Procedures.

Requirements

  • You hold a University degree in health related field or computer science or equivalent experience
  • You have an internship experience or a 1st working experience in Data Entry and Data Review
  • You prove experience in using word processing software and spreadsheets (MS Word, Excel)
  • You have good communication and interpersonal skills
  • You are accurate and pay attention to details
  • You are able to work in team environment
  • You have a working knowledge in English
  • An existing right to work in Europe is required

Benefits

  • A balanced salary package based on your capabilities and experience
  • Hybrid working opportunity (min. 1 day/week on site)