Clinical Research Associate (Experienced)
Medpace, Inc.
Netherlands
Hybrid
Intermediate
posted 1 day ago
Vacancy Summary
Join our rapidly growing Clinical Operations team in the Netherlands as an Experienced Clinical Research Associate. This role offers an exciting opportunity to leverage your expertise while further developing your career in clinical research.
Our clinical activities are expanding, and we are looking for an Experienced Clinical Research Associate to be part of our Clinical/Country Operations team in the Netherlands. You will collaborate with a team to execute tasks and projects essential to the company's success. If you are seeking a dynamic career where you can apply your previous experience and continue to grow, this is the opportunity for you.
Medpace is a full-service clinical contract research organization (CRO) that provides 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 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 over 6,500 people across more than 40 countries.
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 worldwide through continuous learning and cross-functional collaboration.
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.
Required skills
communication
Methodologies
Techniques
Clinical Development
Clinical Research
SAFe
Cross-functional Collaboration
Operations
monitoring
Oncology
Interviews
service
Document Verification
Cutting
Dutch
English
Compensation
Reporting
Therapy
Document Review
Flexibility
influence
Professional Development
CRA
Science
Health
CAN
events
Clear
Training
Management
retention
Performance
Learning
Onboarding
Site Initiation
Culture
Forms
Therapeutic Expertise
Case
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Benefits
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