Manager Data Intelligence

• Collects validates and maintains data from internal and external sources to support feasibility and operational activities.
• Analyses clinical trial site investigator and operational data to identify trends patterns and opportunities for improvement.
• Develops and maintains standard reports dashboards and data visualizations to support stakeholder decision-making.
• Supports feasibility assessments by providing data summaries analyses and insights related to study requirements site performance recruitment trends and therapeutic areas.
• Collaborates with Operational Strategy Clinical Operations Business Development and other functional stakeholders to understand data needs and deliver timely analyses.
• Performs data quality reviews and works to resolve data inconsistencies and gaps.
• Identifies opportunities to improve existing data collection reporting and analytical processes.
• Supports the evaluation and integration of new data sources tools and technologies.
• Maintains documentation related to data sources methodologies reporting processes and best practices.
• Develops and updates reporting templates and analytical tools to improve efficiency and consistency.
• Provides ad hoc analyses and reports in support of departmental and organizational priorities.
• Monitors key operational and feasibility metrics and communicates findings to stakeholders.
• Supports process improvement initiatives by leveraging data to identify efficiencies and operational enhancements.
• Ensures compliance with applicable quality standards policies and data governance requirements.
• Performs other duties and special projects as assigned.

Qualifications :

• Bachelors degree in Life Sciences Data Analytics Health Sciences Business Statistics Public Health or a related field required. Masters degree in a relevant discipline preferred.
• Strong experience in clinical research feasibility clinical operations data analytics business intelligence or a related field.
• Experience working with clinical trial investigator site operational or healthcare-related datasets.
• Demonstrated experience analysing and interpreting complex data from multiple sources.
• Experience developing reports dashboards and data visualizations for business stakeholders.
• Experience working within a CRO pharmaceutical biotechnology healthcare or related environment preferred.
• Experience supporting feasibility assessments site selection activities clinical operations or operational planning preferred.
• Experience collaborating with cross-functional teams in a global environment.
• Knowledge of clinical development processes and clinical trial conduct is desirable.
• Experience with business intelligence and reporting tools such as Power BI Tableau Spotfire or similar platforms preferred.

Additional Information :

When you join Ergomed Group you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. Youll join a passionate and collaborative team of experts in clinical research pharmacovigilance and quality consulting.  

We are diverse in many ways yet our values unite us. Our values are how we work not words on a wall. If they sound like you you will feel at home here. 

• Quality: we hold ourselves to the standard patients deserve. 

• Integrity and trust: we do the right thing especially when it is hard. 

• Drive and passion: we care about the outcome because someone is waiting on it. 

• Agility and responsiveness: we move quickly because patients cannot wait. 

• Belonging: everyone is welcome and every voice counts. 

• Collaborative partnerships: we go further by going together. 

We look forward to welcoming your application. 

Remote Work :

Yes

Employment Type :

Full-time