💼 Job Opportunity: Research Associate III at Advarra
✨ Why Join Advarra?
- 🌟 Mission-Driven Work: Contribute to advancing clinical research that improves lives.
- 🤝 Inclusive Culture: Collaborative environment valuing diversity, equity, and inclusion.
- 🚀 Professional Growth: Opportunities to use cutting-edge clinical trial management tools.
📋 Job Description:
🔹 Role: Research Associate III
🔹 Key Responsibilities:
- 📊 Interpret clinical trial protocols to design study calendars and budgets.
- 📝 Develop case report forms (CRFs).
- 💻 Utilize Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) systems.
- 🤝 Collaborate with managers to ensure high-quality deliverables.
- 📈 Track and report progress using internal tools.
- 💡 Participate in team discussions for better project outcomes.
🎓 Qualifications:
✅ Basic:
- 📅 2+ years of clinical research experience.
- 📜 Knowledge of Good Clinical Practice (GCP) and regulations.
- 💼 Proficient in MS Office and business software.
- 🤝 Strong organizational and teamwork skills.
💡 Preferred:
- 🧑⚕️ Experience as a clinical trial coordinator, data manager, or pharmacovigilance professional.
- 🗂️ Background in records management or clinical operations.
📌 How to Apply:
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