Nurse Practitioner - Diabetes & Endocrine

Medpace•Cincinnati, OH

62d

About The Position

We are seeking Nurse Practitioners with diabetes or endocrine experience to join our dynamic team. In this role, you will work side by side with our physicians, serving as a clinical expert, to support our project teams in clinical research studies. If you are interested in contributing to innovative clinical research in a highly collaborative environment, this is the right opportunity for you. 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 5,000 people across 40+ countries. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Requirements

Masters or doctorate degree
Active Nurse Practitioner license
At least 1-2 years of clinical experience as a Nurse Practitioner specializing in diabetes/endocrine patient care

Nice To Haves

Prior clinical research experience preferred
Experience working with adult or pediatric populations using continuous glucose monitors (CGMs) preferred.

Responsibilities

Develop and implement disease-specific and clinical education for internal teams
Review study and study participant clinical safety data (e.g. laboratory, medications, medical history) as an integral part of the study's medical monitoring team
Review assigned protocols for scientific and participant safety matters and risks
Attend pre-study and study-related meetings with project teams, providing clinical expertise
Assist the Clinical Operations team with activities related to study participant recruitment, screening and study conduct
Participate in new business activities by providing clinical input in Medpace's written proposals for conducting a client's clinical trial
Serve as a clinical expert in business presentations to new clients