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Clinical Data Visualization & Reporting Analyst, preston, lancashire
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Client:
Meet Life Sciences
Location:
preston, lancashire, United Kingdom
Job Category:
Other
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EU work permit required:
Yes
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Job Views:
2
Posted:
31.05.2025
Expiry Date:
15.07.2025
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Job Description:
About the Role
We are seeking a Clinical Data Visualization & Reporting Analyst to support critical functions in clinical trial operations. This role contributes to data-driven decision-making by developing advanced reports and dashboards for medical monitoring, safety review, data quality management, and other cross-functional business needs.
The ideal candidate will be analytical, detail-oriented, and comfortable working with clinical data and visualization tools. You’ll partner closely with cross-functional stakeholders—including Clinical Operations, Data Management, Medical Affairs, and IT—to create impactful visualizations that support clinical development activities.
Responsibilities
Depending on experience level (Entry through Expert), responsibilities may include:
* Developing dashboards and reports for medical safety review, risk-based monitoring, biomarker evaluation, and other clinical trial activities.
* Collaborating with internal stakeholders to translate business needs into technical solutions.
* Supporting integrated reporting and metrics development aligned with clinical and strategic goals.
* Participating in lifecycle and change management of analytics platforms.
* Contributing to system and performance optimizations.
* Mentoring junior team members and leading reporting development (advanced/expert levels only).
Key Tools & Technologies
* Visualization Tools: Tibco Spotfire, Tableau, Power BI, or QlikView
* Data Management & Querying: SQL, ETL pipelines, Data Warehousing (e.g., ODW)
* Collaboration & Platforms: SharePoint, clinical trial data platforms
Qualifications
Entry Level:
* Bachelor's degree in a technical field (Engineering, Computer Science, Life Sciences, or Statistics).
* Some experience with clinical data and reporting tools in a regulated environment.
Base Level (1–3 years):
* Experience in a clinical trial or regulated industry environment.
* Working knowledge of visualization tools and SQL.
* Familiarity with SDTM or other clinical data models preferred.
Advanced Level (4+ years):
* Strong experience in data visualization within clinical trials.
* Advanced skills in reporting tools and scripting languages.
* Ability to independently manage complex reporting tasks.
Expert Level (6+ years):
* Deep expertise in data analytics and clinical reporting.
* Proven ability to lead projects and mentor teams.
* Familiarity with CDISC standards and advanced reporting infrastructure.
Desired Competencies
* Strong analytical and problem-solving skills
* Excellent communication and stakeholder management
* Experience working in a matrixed, cross-functional team
* Ability to manage multiple priorities in a fast-paced environment
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