Manager, Phase II/III Research - Full Time - Wolf River
On-siteGermantown, Tennessee, United States
Job Summary
Oversee daily Phase II/III clinical trial activities by supervising Clinical Research Coordinators, assigning projects, and monitoring workloads to ensure efficient study execution. Recruit and screen subjects for eligibility while educating nursing staff and patients on protocol therapies, medication schedules, and side effect management. Collaborate with physicians, academic partners, and sponsors to develop study protocols, informed consent documents, and data capture portals, while managing relationships to maintain the research portfolio. Facilitate audits, maintain regulatory compliance with Code of Federal Regulations, and protect participant rights throughout each study. No nights, weekends, or holidays; comprehensive benefits package available.
Required Qualifications
- Bachelor's degree from an accredited four-year college or university
- minimum of three (3) years of related experience
- five (5) to seven (7) years of related experience and/or training in a healthcare or clinical research environment
- equivalent combination of education and experience
- Excellent organizational and follow-up skills
- Excellent verbal and written communication skills
- Strong problem-solving skills with the ability to organize and prioritize work assignments
- Ability to manage multiple priorities in a fast-paced environment
- Ability to analyze situations and respond in a timely manner
- Ability to work effectively within multidisciplinary teams
- Ability to establish and maintain effective working relationships throughout West Cancer Center
- Proficiency in computer applications, including word processing and email
- Ability to read, analyze, and interpret financial reports, government regulations, scientific journals, technical documents, and legal documents
- Ability to communicate effectively both verbally and in writing with customers, regulatory agencies, and members of the business community
- Ability to effectively present information to leadership, employee groups, and public audiences
- Ability to calculate figures and amounts, including discounts, percentages, body surface area (BSA), absolute neutrophil count (ANC), drug calculations, area, circumference, and volume
- Ability to apply concepts of basic algebra and geometry
- Ability to define problems, collect data, establish facts, and draw valid conclusions
- Ability to interpret complex technical instructions and manage multiple abstract and concrete variables
- Ability to work near toxic or caustic chemicals
- Ability to lift up to 10 pounds
- Additional hours
- Travel
Desired Qualifications
- Clinical research certification through SoCRA or ACRP
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.