Clinical Data Associate

Summary

Experienced researcher and project administrator with 5 years of experience working in Biomedical and Clinical Research. As a researcher, I am adept at collecting and analysing data to extrapolate meaningful conclusions. As a project administrator, I am skilled in communication, teamwork and managing multiple deadlines. My exposure to global clinical operations over the last several years has led to my interest in the area of Clinical Data Management.

I am an analytical and critical thinker, as such I have always enjoyed the opportunity to problem solve and improve processes in each role that I have held. My high degree of organization and attention to detail has been crucial to my success in managing various projects throughout my career.

My therapeutic expertise is in oncology and particularly immuno-oncology. I am passionate about biology as it applies to medicine and enthusiastic about delving into new therapeutic areas adapting to new challenges is one of my strengths. Ultimately, I aspire to be in a position to make use of my scientific content expertise to contribute to the improvement of patient care.

Please feel free to reach out or connect!

Native English Speaker | Dual Citizen USA/European Union | EU Driver's License Category B

Expectations

With a few years of professional experience under my belt, I am looking for an opportunity to put my skills and education to use within the Life Sciences and/or Clinical Research industry. More important to me than any other factor is the opportunity to learn, develop and be challenged. I am open-minded as to what specific path I take, so long as the role involves my key strengths and interests: problem-solving and analytical thinking.

Employment Preferences

Expected Base Salary

**,000 EUR

Expected Hourly Rate

** EUR/hr

Academic Degree

Experience

Skills

• Research
• Good Clinical Practice
• GCP
• Project Coordination
• Scientific Writing
• Editing
• Molecular Biology
• Data Analysis
• ELISA
• Cell Culture
• Biology
• Real-Time Polymerase Chain Reaction
• QPCR
• Flow Cytometry
• Western Blotting
• Clinical Research
• Immunology
• Clinical Trials
• Medical Terminology
• Oncology
• Risk Assessment
• Proofreading
• Project Management
• Documentation
• Publications
• Electronic Data Capture
• EDC
• Standard Operating Procedure
• SOP
• Data Management
• Project Teams
• Clinical Trial Management System
• CTMS
• Electronic Trial Master File
• ETMF
• Microsoft Office
• Veeva Vault
• Microsoft Excel
• Microsoft Word
• Microsoft Outlook
• Microsoft PowerPoint
• Teamwork
• Time Management
• Employee Training
• Communication
• Decision-Making
• Critical Thinking
• Customer Service
• Oncology Clinical Research
• Team Coordination
• Medidata
• RAVE
• PubMed
• MedDRA
• CDISC Standards
• REDCap