Clinical Trial Data Analyst (talent pool)

☞ PharmiWeb.Jobs

Ver: 145

Dia de atualização: 16-11-2025

Localização: Mechelen Antwerp

Categoria: IT - Software

Indústria: Staffing Recruiting

Posição: Associate

Tipo de empregos: Full-time

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Conteúdo do emprego

Join our pipeline of candidates for our future recruitment needs in our Project Management department!

If you are looking for a company where you can personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view, consider working at Labcorp Drug Development as a Clinical Trial Data Analyst.

About The Position

The Clinical Trial Data Analyst (Global Monitor) will create and maintain the Global Monitoring plan for the assigned studies, coordinate the work of Client Coordinator Specialists, Global Monitoring Center and Regional Study Coordinators and ensure regular communication with the Global Study Managers or Global Study Leads who are accountable for the entire protocol.

Responsibilities/Duties
  • Leverages therapeutic area, client and study type knowledge to create and maintain a study specific monitoring and data lock plan
  • Liaises with internal teams to ensure monitoring needs for a study can be met with quality
  • Ability to create and motivate a team around project deliverables
  • Provides data focused impact assessments as needed
  • Triage of new work requests
  • Liaises with Developers to ensure development of monitoring tools are completed to the client’s specifications
  • Delegates/generates reports related to monitoring activities
  • Reviews/analyzes data within monitoring scope
  • Suggests actions/changes to the Global Study Manager based on data analysis
  • Escalates issues, highlights trends and liaises closely with Global Study Manager or Global Study Lead throughout life of the study to ensure monitoring is appropriate
  • Supports Risk Management Plan creation and ongoing maintenance through monitoring, analysis
  • Participates in functional meetings (e.g. CLFs) and provides input, keeping processes up to date
  • Complies with the Global Project Management strategy
  • Supports a culture of continuous improvement, quality and productivity
Education
  • University Degree required; Masters or PhD in scientific field preferred
Experience
  • 5-7 years of related experience (Education can substitute for work experience) in project management, data analysis for the pharmaceutical/healthcare industry
  • Demonstrated advanced level knowledge of Excel, Access and other monitoring tools.
  • Curious, data driven analytical thinker
  • High degree of motivation, flexibility and creativity
  • Big picture thinker who suggests changes to process, identifies risks and potential opportunities for data improvement
  • Strong problem-solving skills
  • Able to operate with minimal guidance while owning deliverables end-to-end
  • Proven ability to effectively communicate ideas/concepts and to motivate others to accomplish challenging shared goals and objectives.
  • Dedication for learning and self-improvement
  • Robust self-organization; at-ease with managing conflicting priorities
  • Strong customer service skills
  • Working proficiency in English
Labcorp Is Proud To Be An Equal Opportunity Employer

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant’s race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement .
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Data limite: 31-12-2025

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