Trial Insights Manager

Novo Nordisk

Gladsaxe Kommune

Vor Ort

DKK 651.000 - 957.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Novo Nordisk in Søborg is seeking a Trial Insights Manager who will lead analyses shaping global Phase I–IV trial location decisions. You will turn multi‑source data into clear, evidence‑based country allocation recommendations for trial planners and Clinical Operations teams.

Your work covers feasibility, enrolment forecasts and operational insights, with a focus on traceability, reproducibility and transparent documentation to support data‑driven decisions across global trials.

Qualifikationen

  • Master's degree or equivalent in life sciences, data science, statistics, economics, engi­neering, business administration or another relevant field.
  • Significant experience in analytics, clinical operations, trial planning, feasibility, data science or related RD/biomedical support.
  • Strong analytical and conceptual problem-solving skills with the ability to handle complexity and ambiguity.
  • Experience with analytical tools such as SQL, Power BI, Python, R, Excel (preferred).
  • Experience with scenario modelling, analytical tool development, data integration, dashboards or reproducible analytics.
  • Experience working with cross-functional stakeholders and translating data into business recommendations.

Aufgaben

  • Lead analytical work packages that support country allocation, feasibility assessment, enrolment forecasting and operational decisions for global Phase I‑IV trials.
  • Define analytical approaches, integrate multiple data sources and run scenario analyses for medium and high complexity planning questions.
  • Develop and quality assure analytical input on country allocation scenarios, recruitment assumptions and operational feasibility.
  • Translate data and insights into clear recommendations and facilitate data-driven dialogue to build alignment.
  • Plan, scope and deliver analytical projects, including stakeholder mapping, timelines and risk identification.
  • Build, test and maintain analytical tools, dashboards, reusable code and data pipelines, driving automation and scalability.
  • Document assumptions, data sources, limitations, methodology and review steps transparently, shaping data/analytics standards.

Kenntnisse

Analytical thinking
Cross‑functional collaboration
Stakeholder management
Communication and presentation
Coaching others
Documentation and traceability
Problem solving in ambiguity
Project management
Training in analytics

Ausbildung

Master's degree or equivalent

Tools

SQL
Power BI
Python
R
Excel

Jobbeschreibung

Your impact begins here

As Trial Insights Manager in Trial Performance Insights, you will lead the analysis that shapes where global Phase I-IV clinical trials run. You will turn data from multiple sources into clear, evidence-based country allocation recommendations for trial planners and Clinical Operations teams. Your work will inform feasibility, enrolment forecasts and operational decisions, helping trials start on solid ground and move forward at pace for people living with serious chronic diseases.

Location: Søborg

Department: Trial Performance Insights

What You'll Bring
  • A Master's degree or equivalent in life sciences, data science, statistics, economics, engineering, business administration or another relevant field.
  • Significant experience in one or more of the following areas: analytics, clinical operations, trial planning, feasibility, data science, consulting or related R&D business support.
  • Strong analytical and conceptual problem-solving skills, and the ability to handle complexity and ambiguity with limited predefined procedures.
  • Strong experience with analytical tools such as SQL, Power BI, Python, R, Excel or similar is preferred; alternatively, a strong background in clinical operations is equally valued.
  • Experience with scenario modelling, analytical tool development, data integration, dashboards or reproducible analytics.
  • Experience working with cross-functional stakeholders and translating complex data into business recommendations.
  • Strong stakeholder management and influencing skills, with clear communication and presentation skills.
  • A quality mindset focused on traceability, reproducibility and documentation.
  • The ability to coach or guide less experienced colleagues.
  • Training in advanced analytics, project management, clinical trial operations or data engineering.
What You'll Do
  • Lead analytical work packages that support country allocation, feasibility assessment, enrolment forecasting and operational decisions for global Phase I-IV trials.
  • Define analytical approaches, integrate multiple data sources and run scenario analyses to deliver robust outputs for medium and high-complexity trial planning questions.
  • Develop and quality assure analytical input on country allocation scenarios, recruitment assumptions and operational feasibility.
  • Translate data and operational insight into clear recommendations, and facilitate data-driven dialogue that explains assumptions and builds alignment.
  • Plan, scope and deliver analytical projects, including stakeholder mapping, timelines and risk identification.
  • Build, test and maintain analytical tools, dashboards, reusable code and data pipelines, and drive automation and scalability of methods and outputs.
  • Document assumptions, data sources, limitations, methodology and review steps transparently, and help shape standards for data, analytics and quality review.
Who You'll Work With

You will join Trial Performance Insights in Research & Development, where colleagues bring together curiosity, data, technology and collaboration to help advance scientific ideas into clinical testing.

Your closest partners will be trial planners and Clinical Operations teams, who rely on your analysis to make country allocation and feasibility decisions. You will also work with colleagues in TP-AP, Global Trial Allocation and related R&D functions to align on assumptions, share better practice and develop common analytical standards. The work covers global trials, so you will bring different perspectives together, create clarity and help teams move from insight to decision.

What You Can Expect Here

You will work on complex questions with real influence on how trials are planned. You are trusted to own your work, make your voice heard and shape the standards and tools your colleagues use. You will grow through hands-on project delivery, collaboration across R&D functions and the chance to coach colleagues, in an environment that supports you to perform at your best.

Salary: For this role, the Annual Base Salary ranges from DKK 651,200 to 956,900, corresponding to the level of the position. The placement within the salary range will be assessed during the recruitment process based on the candidate's skills, competencies, knowledge, and relevant experience.

Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

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