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Medical Data Specialist Zaventem (BE) Oxford Global Resources

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Gevraagd

  • 37 - 40 uur
  • Engels (taal)

Aanbod

  • Vast contract
  • Deels thuiswerken
 

Vacature in het kort

Zaventem (BE)
A Medical Data Specialist is needed to join a team in Belgium. The role involves working with Clinical Database Developers and Managers to review and process clinical data, ensuring accuracy and compliance with study protocols. Tasks include database testing and site support. Enjoy the benefits of a hybrid working model, with office presence required only three times a week for a few hours. Join a collaborative team and make a difference in clinical data management. Read on for more information about this exciting opportunity.
 

Over het bedrijf

Oxford Global Resources
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Volledige vacaturetekst

For one of our clients located in the north of Brussels, we are looking for a Medical Data Specialist to join their team in Belgium.

Job Description

In this role, the Medical Data Specialist will work closely with Clinical Database Developers and Clinical Data Manager leads. The primary focus will be on reviewing and processing clinical data to ensure that all collected data is accurate, compliant, and consistent with the clinical study protocol. The Medical Data Specialist will also work on additional activities including database testing and site support.

Responsibilities

  • Review clinical data for completeness, accuracy, and consistency in accordance with the investigational plan
  • Develop and maintain data management documentation and guidelines in line with Good Clinical Practices (GCP) and Good Documentation Practices (GDP)
  • Perform regular data cleaning tasks (e.g., listings review, query management) following Data Management processes and the Data Management Plan
  • Provide regular updates and escalate issues to study functional leads
  • Provide direct support to the project team on data management activities, if required
  • Maintain compliance with corporate, core, and study-specific learning requirements
  • Collaborate closely with cross-functional teams, including Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs), to ensure data integrity and alignment with study objectives

Requirements

  • Master's degree in Life Sciences
  • Ideally, 1-2 years of experience in clinical data management or clinical data cleaning. Junior candidates with min 4-6-month internship in clinical data management within the industry or a CRO, and holding an ICH-GCP certification will also be considered.
  • Fluent in English, with strong communication skills and the ability to collaborate effectively in a global team environment
  • Basic knowledge of programming languages (e.g., SQL) is a plus. Experience using data processing tools such as Excel, SAS, R, or Python is an asset.
  • Strong organizational and analytical skills, with a solution-oriented mindset and a positive attitude
  • Existing right to work in Europe is required

Additional Information

  • Start Date: ASAP (October 1st the latest)
  • Schedule: full-time
  • Permanent Contract with Oxford Global Resources
  • Hybrid working model (Presence in the office is required 3 times/week (It can be limited to a few hours during the day)
  • Client's location : north of Brussels

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