Intern, Clinical Data Programmer and Clinical QA

The Clinical Data Programmer and Clinical QA Intern will help provide the Terumo Neuro (TN) Clinical Research & Operations (CR&O) Team with high-quality clinical data in various formats inclusive of (but not limited to): data visualization from multiple clinical systems to help develop the Critical to Quality (CtQ) metrics for risk review and make the best mitigation decisions upon based on the high-quality available evidence. 

 Working with TN CR&O, you'll expand your scope, including an introduction to Good Clinical Practice (GCP), hands-on experience in dealing with real medical device clinical data with opportunities to develop dashboards, metrics, and other visualizations. 

You will primarily be responsible for learning from and working with the guidance of a Clinical Data Manager, Clinical Quality Assurance Manager, and Clinical SAS Programmer team member as to how to plan and execute programming in support of (but not limited to): 

1. Collaborate with clinical research personnel to understand the CtQ metrics that need to be tracked 

2. Develop intuitive CtQ Reports, Dashboards, and Data Visualizations that represents Quality Tolerance Levels (QTLs) and Key Risk Indicators (KRIs) of Clinical Studies 

3. Assist in preparing reports and presentations based on dashboard insights for key stakeholders 

4. Ensure accuracy and integrity of data presented in the dashboard 

5. Attend clinical study team and cross functional team (CQA and DM) meetings and provide updates on project process 

• Working toward a Bachelor or Master’s degree in Mathematics, Statistics, Computer Science, Life Sciences or Health Sciences, or other related majors. 

• Competent in at least one programming language (SAS, R, or Python) 

• Fluency in using data visualization tools (e.g., Power BI, Tableau, or IBM Cognos) 

• Proficiency with Microsoft Word, Excel, PowerPoint, Notepad (or Notepad++) 

• Desire to be part of a rapidly evolving organization where you will showcase your decision-making, leadership, project management, collaboration, and problem-solving skills 

• Strong analytical skills and attention to detail 

Desired Qualifications 

• Strong analytical capability and organization skills 

• Prior experience in at least one programming language (e.g., SAS, R, or Python) 

• Prior and/or project experience with visualizing data (e.g., Critical to Quality (CtQ) Reports, Quality Tolerance Levels (QTLs), or Key Risk Indicators (KRIs) Metrics)) 

• Prior and/or project experience using data visualization tools (e.g., Power BI, Tableau, or IBM Cognos) 

• Good interpersonal and communication skills and the ability to work effectively in a team environment as well as autonomously in a remote environment  

• Knowledge of medical device industry 

What you will Gain

1. Hands on experience in data analysis and visualization within the clinical research and quality assurance field 

2. Opportunity to work alongside experienced professionals in clinical trials and data analytics 

3. Development of technical and soft skills that are valuable in the medical device industry 

Additional Information 

•   The primary work location for this position is Aliso Viejo, CA (company headquarters). Hybrid – remote/in-office option. 

• Candidates must be eligible to work in the U.S. and not require visa sponsorship. 

• Relocation may be available for qualified candidates. 

• For more information, visit our web site at www.microvention.com