Work Flexibility: Hybrid

What will you do:

• Develop Power BI dashboards, reporting tools, and user-friendly data products that enable stakeholders to access insights independently and reduce reliance on manual reporting processes.

  
  
  

• Design, develop, andmaintainautomation solutions using Power Automate, APIs, and other technologies to streamline evidence management, reporting, data updates, and operational workflows.

  
  
  

• Develop integrations between platforms, applications, and data sources to enable efficient information flow, reduce duplicate effort, and improve the overall user experience.

  
  
  

• Develop validation processes, quality checks, and monitoring approaches that improve confidence in data used across the organization.

  
  
  

• Create reusable tools, workflows, and technical solutions that can beleveragedacross multiple projects and business needs.

  
  
  

• Serve as the technical lead for Clinical Data Sciences automation, BI, and technology initiatives.

  
  
  

• Collaborate with stakeholders across Clinical Research, Medical Affairs, Regulatory Affairs, Market Access, and other functions as needed to support CDS-led initiatives and ensure solutions align with businessobjectives.

  
  
  

• Partner closely with the Clinical Data Sciences Manager and growing CDS team to translate strategic priorities, business needs, and evidence management challenges into scalable technical solutions

  
  
  

What will you need:

Basic qualifications:

• Master’s degree in a scientific or healthcare-related field.

  
  
  

• Minimum8-10years of experience in clinical data management or a similar role in the pharmaceutical or clinical research industry. Experience in medical devicescompanyis preferred.

  
  
  

• Strong understanding of clinical trial processes, data managementprinciplesand regulatory guidelines.

  
  
  

• Proficiencyinautomation, Microsoft PowerSuiteand clinical data management software.

  
  
  

• Familiarity with relevant regulations and guidelines, like GCP and CDISC standards.

  
  
  

• Knowledge of industry-standard data analysis and reporting software, such as SAS,SQLand/or Oracle Clinical.

  
  
  

• Excellent attention to detail with problem-solving and analytical skills.

  
  
  

• Strong organizational and time management abilities.

  
  
  

Preferred qualifications:

• Certification in clinical data management (like CCDM).

  
  
  

• Knowledge of MS Project and analytical capabilities.

  
  
  

• Knowledge of CDISC standards and data interchange formats (e.g., SDTM,ADaM).

  
  
  

• Familiarity with clinical trial design and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP).

  
  
  

• Understanding ofdata privacy and protection regulations (e.g., GDPR).

  
  
  

• Effective communication and interpersonal skills to collaborate with other teams.