Job Description
Job Duties & Responsibilities: Coordinating project activities and collecting essential study data and documents as outlined in protocols. Building and maintaining strong relationships with key contacts at sites Preparing, managing, and organizing internal and external communications with sites Creating and updating content such as presentations, newsletters, forms, and diagrams Serving as a resource to other study staff on study conduct, documentation, communication, and regulatory compliance Participating in team and site training
Qualifications, Knowledge/ Skills & Abilities Strong ability to plan, coordinate, and execute multiple activities proactively with a high sense of urgency, quality, and follow-through. Experience working both in a team environment as well as independently. Confidence interacting with providers, operational teams, and clients. Multi-tasking in a fast-paced environment Demonstrate an understanding of applicable policies and procedures. Maintain conditions that ensure a healthy and safe working environment. Take ownership and hold themselves and others accountable for delivering results that matter.
Requirements
Bachelor’s degree in a related field 2+ years of full-time professional experience High proficiency in Microsoft Office products (Outlook, Excel, Word, PowerPoint) Experience with electronic health records preferred.