Research Associate II Specialist
5 days ago
This is a challenging and rewarding opportunity to work as a Clinical Research Associate (CRA) with Advarra. As a key member of our team, you will be responsible for coordinating and managing clinical trials from start to finish.
Key Responsibilities- Study Coordination: Understand and interpret clinical trial study protocols to design and develop calendars. Collaborate with internal teams to ensure timely completion of tasks and meet quality standards.
- Data Management: Design and develop case report forms for clinical trial study protocols. Develop a familiarity with Advarra's Clinical Trial Management Software (CTMS) and Electronic Data Capture (EDC) software.
- Financial Management: Work closely with reporting managers to complete daily/weekly calendars, budgets, financials, and/or case report forms design to meet pre-determined quality criteria.
- Experience: 1+ year of relevant experience in clinical research or a related field.
- Skills: Strong organizational and administrative abilities. Knowledge of clinical research methodology, industry regulations, and Good Clinical Practice guidelines related to human research.
This role offers a competitive salary of $45,000 per year, as well as opportunities for growth and development within the company. We also offer a range of benefits, including health insurance, retirement planning, and paid time off.
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