CLINICAL DATA ASSOCIATE SKILLS, EXPERIENCE, AND JOB REQUIREMENTS

Published: July 15, 2024 - The Clinical Data Associate possesses extensive experience in clinical data management and analytics, leveraging tools such as Oracle Clinical, Medidata, and IBM Clinical Development. This role involves thorough knowledge of ICH/GCP guidelines and a robust capability in data handling for clinical trials. The associate is highly organized, detail-oriented, and proficient in Google Sheets and Microsoft Excel, ensuring meticulous execution of responsibilities within tight deadlines.

Essential Hard and Soft Skills for a Standout Clinical Data Associate Resume
  • Data Management
  • Analytics Skills
  • Oracle Clinical Proficiency
  • Medidata Proficiency
  • TrialMaster Skills
  • IBM Development Skills
  • ICH/GCP Knowledge
  • Data Handling
  • Google Sheets
  • Microsoft Excel.
  • Detail Attention
  • Critical Thinking
  • Learning Aptitude
  • Organizational Ability
  • Self-Motivation
  • Deadline Management
  • Problem Solving
  • Communication
  • Teamwork
  • Adaptability.

Summary of Clinical Data Associate Knowledge and Qualifications on Resume

1. BS in Biostatistics with 3 years of Experience

  • Proficiency in Microsoft Office Word, Excel, PowerPoint, Outlook
  • Able to handle a variety of clinical research tasks
  • Excellent organizational and communication skills
  • Requires good attention to detail, excellent documentation skills and works well in a group environment
  • Flexible agile teammate who can change activities and directions quickly and respond to a variety of assignment and changing business needs
  • Able to read, write, speak fluently, and comprehend the English language
  • Experience in a clinical, scientific, or healthcare discipline
  • Knowledge of Federal information technology, the Biotech or Pharmaceutical Industry, or equivalent comparable background.
  • Experience with clinical trial databases and electronic data capture (EDC).
  • Experience with GCP and Human Research Subjects Protection guidelines, as well as regulatory requirements relating to clinical development and compliance with safety, ethical, legal, and regulatory standards.

2. BA in Health Informatics with 2 years of Experience

  • Experience in technical 
  • Exceptional attention to detail with the ability to meet aggressive deadlines
  • Need to be flexible, proactive, and resourceful with a high level of professionalism.
  • Good documentation skills
  • Ability to access information from databases and reports
  • Prefer candidate with some experience in SQL, JMP and Excel.
  • Able to work comfortably in a fast-paced environment with quickly shifting priorities
  • Skills in prioritization, organization, and time management.
  • Experience with clinical/medical terminology.
  • Good communication skills

3. BS in Clinical Data Management with 4 years of Experience

  • Experience in clinical data management or data analytics
  • Experience in scientific research in any capacity
  • Experience in data management.
  • Experience with Oracle Clinical, Medidata, OmniComm TrialMaster, and IBM Clinical Development
  • Experience providing knowledge of ICH/GCP guidelines and applicable regulatory requirements
  • Experience in data handling and Clinical trial experience
  • Attention to detail, Critical thinking skills
  • Strong aptitude for learning new software programs
  • Organized & self-motivated, able to meet tight deadlines
  • Proficiency in Google Sheets or Microsoft Excel