Cincinnati, OH30+ days ago
Assist with study participant screening, admission, orientation, conduct, and discharge; • Demonstrate technical skills in phlebotomy, laboratory specimen collection, electrocardiogram placement, vital signs, and other protocol-related procedures; • Assess, document, and notify appropriate project team members of study participant adverse events in timely manner; • Assist other clinical staff with study-related duties (e.g., laboratory draws, electronic data capture entry, queries, follow-up appointments); • May coordinate studies including working with the research team on development of overall study processes in accordance with the protocol, obtain informed consent, conduct study visits, maintain accurate investigational drug accountability when dispensing study drug. Flexible work environment Competitive PTO packages, starting at 20+ days Competitive compensation and benefits package Company-sponsored employee appreciation events Employee health and wellness initiatives Community involvement with local nonprofit organizations Discounts on local sports games, fitness gyms and attractions Modern, ecofriendly campus with an on-site fitness center Structured career paths with opportunities for professional growth Discounted tuition for UC online programs Awards.