Excellent computer (word-processing, databases, Excel, Windows) skills
Very good level of English. Should be able to communicate fluently and write documents
Good organizational and communication skills
No travel required.
We kindly request to submit CV in English.
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 rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
Collaborative Culture
Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
Leadership throughout Medpace is both accessible and approachable
Continuous Growth & Development
Office based environment with on-site mentors
Defined career paths with clear advancement opportunities
Industry renowned onboarding and training programs designed to accelerate professional development
Ongoing training and continuous learning opportunities throughout your career
An environment that encourages employees to influence change, contribute ideas, and grow quickly
Other Employee Benefits
Competitive compensation programs that recognize and reward performance
Comprehensive health, wellness, retirement, and PTO benefits
Office based culture with occasional WFH that provides flexibility for eligible positions after training
Company-sponsored social events
Please note benefits may vary based on country.
What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.
Work on several projects with different teams (US, APAC and Europe) interacting with Project Managers, other Project Coordinators, Project Assistants and Technologists
Quality control (QC) of the incoming medical imaging/cardiovascular data
Communicate daily with sites (hospitals) all around the world for qualification, data follow up and queries
Draft and maintain study-related documents (in English)
Overall meeting support : organization, agenda, meeting minutes, attendance sheet.
Support the Project Manager on daily activities (such as data export or report requests, databe validation and QC, trackers update, Trial Master File related tasks, etc.)
Coordinate media shipments
BSc, MSc and PhD in Biomedical Engineering or science or medical related field, clinical trials or related field
Prior experience with clinical trials is a plus (clinical research associate are welcome to apply)
Prior experience as a Project Coordinator within a CRO or a pharma company is preferred
Knowledge of Medical Imaging desirable but not mandatory
Understanding of International Conference on Harmonization (ICH)-Good Clinical Practice (GCP) guidelines and other regulatory requirements that may impact clinical trials (FDA, EMA, etc.)
Excellent computer (word-processing, databases, Excel, Windows) skills
Very good level of English. Should be able to communicate fluently and write documents
Good organizational and communication skills
No travel required.
We kindly request to submit CV in English.
