About the Role
This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous nursing expertise and can develop and grow your career even further, then this is the opportunity for you! Stable schedule with no weekends, no work on Medpace holidays, and flexible work schedule.
Responsibilities
- Comprehensive manual review of clinical data collected in trials
- Development of clinical review guidelines for specific therapeutic areas
- Interface with Data Management team to assure query resolution
- Seeking specialization in Oncology
Requirements
- Professional / or Post-Qualification Nursing experience, preferably in Oncology
- General knowledge of clinical trial processes and/or experience working with clinical data
Location
- Office-based
Work Type
- Full-time
Education Level
- Bachelor’s Degree in Nursing, or more advanced clinical degree
Benefits
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
About the Company
- Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
- Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.
- We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
- Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
