Junior Business Analyst – GxP & LIMS

Søborg

We are looking for a Data Scientist for our client in the Pharma industry Job Description We are looking for a Data Scientist to work on projects focused on developing predictive models for treatment outcomes in clinical trials. You will work with harmonized data from multiple RCTs, building and validating machine learning models, with direct impact on future trial design and clinical decision-making. Required Skills Experience working with healthcare data (clinical trials or RWE), including familiarity with standard data structures and common data quality challenges Strong foundation in both statistical modeling and machine learning approaches (regression, classification, regularization, ensemble methods) Understanding of RCT methodology, causal inference, and treatment effect estimation Experience working with longitudinal and time-series data, including handling of missing data and irregular observation schedules Proficiency in Python and/or R and experience working in cloud-based data platforms Strong communication skills and ability to translate complex analytical findings for both technical and non-technical audiences A PhD with 1+ year of relevant experience or a Master's with 3+ years of relevant experience Experience building interactive dashboards and data visualization tools (e.g., R Shiny) Prior experience in pharmaceutical drug development, health economics, or related life sciences fields Start date: 01-06-2026 End date: 18-12-2026 Location: Søborg, Denmark For the duration of this assignment Ework Services (0,9%) will be deducted from the total amount invoiced. We offer candidates continuously. This means that we sometimes remove the assignments before deadline. If you are interested, we recommend that you apply immidiately.

København

We are looking for a Senior Portfolio & PMO Transformation Lead for our client in the Financial Industry We are seeking external consultant support with strong experience in portfolio management, large‑scale transformations, and establishment or maturation of PMO/TMO functions. The organisation operates in a complex environment where large transformation initiatives, multiple projects, ongoing development, and BAU activities must be managed in parallel, while adapting to being part of a larger group. This requires clear portfolio oversight, prioritisation, and executive decision support. External consultants are engaged primarily to bring proven experience, frameworks, and practical know‑how, ensuring a structured and effective setup from the outset. The need is focused on the initial establishment phase, not long‑term operational support. Digital tools (incl. Jira) are used to support execution and reporting, but the emphasis is on portfolio governance, transparency, and decision‑making rather than tool configuration. Consultant setup Consultant must be based in Denmark and able to be present in the office We are open to: 1 full‑time consultant with broad portfolio / transformation experience, or 2 part‑time consultants, combining: Strong portfolio management / PMO / transformation experience Supporting experience with portfolio or delivery tools Must have experience Portfolio management in complex organisations with transformations, projects, development, and operations running in parallel Experience establishing or strengthening PMO / TMO or portfolio governance Experience from regulated environments (banking, pension, financial services) Ability to translate governance and portfolio needs into pragmatic processes and tool usage (tool agnostic mindset) Start date: 01-06-2026 End date: 30-09-2026 Location: Copenhagen, Denmark For the duration of this assignment Ework Services (0,9%) will be deducted from the total amount invoiced. We offer candidates continuously. This means that we sometimes remove the assignments before deadline. If you are interested, we recommend that you apply immediately.

København

We are looking for 1-2 Senior Test managers for Transformation Program in NLP for our client in the Financial Industry The Test Managers will be working with the following: Test planning Test estimation Test koordination Test reporting Test follow up Test execution Required Skills: 10+ Years of Test Management experience Pension domain knowledge Experience with Azure and large complex IT landscapes Good communicator Start date: 01-06-2026 End date: 30-11-2026 Location: Copenhagen, Denmark For the duration of this assignment Ework Services (0,9%) will be deducted from the total amount invoiced. We offer candidates continuously. This means that we sometimes remove the assignments before deadline. If you are interested, we recommend that you apply immediately.

Søborg

We are looking for a Senior Veeva Safety Consultant / Business Administrator for our Client in the pharma industry Job description We are looking for an experienced consultant to join our Safety Operations PV Technology team, with a focus on delivering Veeva Safety advanced business administration and support tasks that allow operational excellence and clæompliance of the pharmacovigilance database and associated systems. This role requires a strong technical foundation, strategic thinking, and the ability to work independently while collaborating across functions. Key responsibilities Lead and deliver Veeva Safety complex business administration tasks related to pharmacovigilance safety database operations and technology integrations, while also supporting the day to day operations, troubleshooting and end user support. Drive and support change implementation, including requirement clarification, impact and risk assessment, creating and execution of test cases and associated coordination. Ensure high-quality execution of tasks to secure compliance with regulatory requirements and internal standards. Contribute to the development and continuous improvement of SOPs and training materials, collaborate with stakeholders to identify leaner ways of working and flag potential risks proactively. Required skills Deep knowledge within Veeva Safety database, including business administrator responsibilities, trial setup, data verification, and release support. Veeva CDMS and clinical trial design knowledge is a plus Demonstrated ability to manage complex tasks with minimal guidance and deliver impactful results. Quality and compliance experience, including GxP validation documentation (e.g. User Acceptance Test plans) Business testing and regulatory compliance. Capable of developing training content and providing super-user support to global stakeholders. Start date: ASAP End date: 26-04-2027 Location: Søborg, Denmark For the duration of this assignment Ework Services (0,9%) will be deducted from the total amount invoiced. We offer candidates continuously. This means that we sometimes remove the assignments before deadline. If you are interested, we recommend that you apply immidiately.