Clinical Research Associate Job at Medpace, Netherlands | Life Science | Apply Online
If you are an experienced Clinical Research Coordinator (CRC), a research nurse, or a patient-facing life sciences professional looking to transition your clinical site knowledge into a high-trajectory international monitoring career, this full-time role at Medpace is an exceptional opportunity. Located at our regional hub in Rotterdam, Netherlands, this position bridges the gap between local site operations and global study execution. For structured coordinators tracking a competitive Clinical Research Associate Job, this position offers entry into the industry-leading PACE training academy, providing a direct pipeline to independent field monitoring. It serves as an elite corporate milestone to launch an exceptional Medpace career and stands out as a premier selection for bilingual professionals looking to secure a high-growth Life Sciences Job with extensive national travel and long-term work-from-home flexibility.
- Job Position: Entry-level Clinical Research Associate – Clinical Research Coordinator experience
- Location: Rotterdam, Netherlands
- Category: Clinical Research Associate
- Job ID: 12511
About The Company
Medpace is a scientifically driven, full-service global Contract Research Organization (CRO) dedicated to providing comprehensive Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, and employing over 6,000 people across more than 40 countries, Medpace is globally recognized by Forbes and Life Science Leader for its disciplined, therapeutic-focused approach to clinical trials. The Rotterdam operations center serves as a key strategic node for the European clinical pipeline. To ensure early-career field monitors transition seamlessly into corporate clinical research, Medpace provides the PACE (Professionals Achieving CRA Excellence) Training Program. This intensive, highly structured initial onboarding framework uses interactive discussions, hands-on practicums, and simulated monitoring exercises to develop your compliance and site management skills, making it one of the most respected CRA acceleration platforms in the industry.
Clinical Research Associate Job – Key Responsibilities
The Clinical Research Associate functions as the primary field representative for the CRO, taking operational ownership of site compliance, data accuracy verification, and patient safety across multi-center clinical trials.
Your core site management, data verification, and clinical monitoring duties include:
- Comprehensive Site Monitoring Visits: Conducting on-site qualification, initiation, routine monitoring, and formal close-out visits for assigned research clinics in strict compliance with the protocol and ICH-GCP frameworks.
- Source Data Verification (SDV): Reviewing and auditing patient medical records and research source documentation against electronic Case Report Form (eCRF) data to identify and correct entry errors.
- Protocol Deviation Triage: Identifying, documenting, and communicating protocol deviations appropriately in accordance with standard operating procedures (SOPs) and regulatory requirements to advance this Clinical Research Associate Job.
- Investigational Product Accountability: Executing meticulous inventory tracking, temperature log reviews, and accountability audits for investigational drugs and medical devices at the site.
- Safety & Adverse Event Verification: Reviewing and cross-checking adverse events (AEs), serious adverse events (SAEs), concomitant medications, and emergent illnesses to confirm accurate safety reporting.
- Investigator Site Communication: Maintaining close, professional contact with clinical research physicians, study coordinators, and laboratory technicians to support your Medpace career.
- Recruitment Strategy Optimization: Assessing patient recruitment and retention metrics at individual clinical sites and offering data-driven suggestions to optimize enrollment.
- Monitoring Report Generation: Authoring detailed, compliant monitoring reports and site follow-up letters summarizing significant findings, deficiencies, and corrective action plans.
Qualifications & Profile Requirements For Clinical Research Associate Job
Medpace seeks a highly analytical, detail-oriented professional who possesses excellent presentation skills, a collaborative mindset, and a valid driver’s license for routine field travel.
- Required Academic & Experience Criteria:
- Educational Foundation: A completed formal Bachelor of Science (BSc) degree in a Health or Life Science related field to qualify for this Life Sciences Job.
- Clinical Research Baseline: A minimum of one (1) or more years of active clinical research experience with direct, patient-facing responsibility as a Clinical Research Coordinator (CRC), Clinical Study Coordinator, or Research Nurse.
- Core Linguistic & Technical Competencies:
- Mandatory Bilingualism: Absolute professional fluency in both written and spoken Dutch and English is required to communicate with local site staff and international study teams.
- Travel Agility: Fully willing and able to travel 60% to 70% nationally across the Netherlands to conduct on-site clinical monitoring visits.
- Solid foundational familiarity with the Microsoft Office suite and an agility to master internally designed, proprietary Clinical Trial Management Systems (CTMS).
- Strong communication, interpersonal, and problem-solving skills, with a zero-error approach to documenting data.
In short, the entry-level CRA position at Medpace is a definitive route to translating your study coordinator experience or research nursing background into a high-prestige international asset. Securing an appointment here allows you to transition away from localized site management and take direct, field-based operational charge of the protocol compliance audits, source data verifications, and investigational product trackings that launch next-generation medical therapeutics. If you reside in or can commute to Rotterdam, meet the mandatory 1-year patient-facing CRC baseline, and possess a fluent command of both Dutch and English, apply today (submitting your application materials in English) to secure this premier selection in a Clinical Research Associate Job, launch an exceptional Medpace career, and lock in this outstanding Life Sciences Job.
