Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based eClinical Coordinator to join our Data Management / eClinical team in Mumbai, India. By working with the eClinical Project Manager and other team members, these professionals ensure the accuracy of data that is reported by patients for clinical studies. If you are detail-oriented, and enjoy a predictable and standardized work environment, this could be the opportunity for you. As new hires, eClinical Coordinators go through an extensive onboarding and training process, which prepares them to become experts in their field.
Responsibilities
Assist the Project Manager in system design and set-up;
Create study specific documents;
Track and provide key study metrics and project monitoring;
Work with clients in obtaining requirements and responding to inquiries;
Other assigned projects and tasks.
Qualifications
Bachelor's degree in a health related field with solid attention to detail and working knowledge of Excel and Word;
Knowledge of medical terminology;
1-2 years of experience in a pharmaceutical or CRO setting preferred.
Preferred Mumbai candidates.
TRAVEL: None
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV 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 the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewardin