Medpace, Inc. logo

Experienced Clinical Research Associate

Medpace, Inc.

Full-time
2-5 years experience
Hybrid

Key Skills

Clinical research
Monitoring
Site initiation
Source document verification
Regulatory document review
Adverse event reporting
Patient recruitment
Medical terminology
Clinical patient management
Drug therapy techniques
Dutch
English

Job Description

Our clinical activities are growing rapidly, and we are currently seeking an Experienced Clinical Research Associate to join our Clinical/ Country Operations team in the Netherlands. 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 expertise and can develop and grow your career even further, then this is the opportunity for you.


Responsibilities

  • Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
  • Perform source document verification and case report form review;
  • Perform regulatory document review;
  • Conduct study drug inventory;
  • Perform adverse event and serious adverse event reporting and follow-up; and
  • Assess patient recruitment and retention.

Qualifications

  • Minimum Bachelor of Science in health-related field; 
  • Previous experience as a CRA;
  • Broad knowledge of medical terminology and clinical patient management;
  • Basic knowledge of drug therapy techniques and clinical research methodologies; and
  • Excellent command of Dutch and English.

We kindly ask to send applications 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.

Core Responsibilities

The Clinical Research Associate will conduct pre-study, initiation, monitoring, and closeout visits for research sites. They are also responsible for performing source document verification, regulatory document review, and managing adverse event reporting.

Requirements

Candidates must hold a minimum of a Bachelor of Science in a health-related field and possess previous experience as a CRA. Proficiency in both Dutch and English is required, along with knowledge of medical terminology and clinical research methodologies.

Benefits

  • Competitive compensation
  • Health benefits
  • Wellness benefits
  • Retirement benefits
  • Paid time off
  • On-site mentors
  • Professional development programs

About Medpace, Inc.

Industry: Pharmaceutical Manufacturing

Company size: 5,001-10,000 employees

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,500 people across 46 countries.

Added Today