Entry-level Clinical Research Associate - Clinical Study Coordinator experience required

Medpace, Inc.; Rotterdam; Hybrid; EUR 60,000 - 90,000; Full time

Benefits offered by this job

Competitive pay

Health & retirement benefits

WFH after training

Social events

Job summary

Medpace is seeking a Clinical Research Associate in the Netherlands to support monitoring visits and site management for pharmaceutical and medical device studies. The role offers training through the PACE CRA program and opportunities to work from home after training, reflecting a mid-size CRO environment with varied daily duties.

The successful candidate will travel nationally up to 60-70% and collaborate with regulatory, medical, and cross-functional teams to ensure protocol adherence and

Qualifications

• Minimum Bachelor of Science in Health or Life Science related field
• 1+ year of clinical research experience with direct patient-facing responsibility
• Willing to travel approximately 60-70% nationally
• Familiarity with Microsoft Office
• Fluent in Dutch and English
• Strong communication and presentation skills
• Valid driver’s license

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
• Communicate with site staff including coordinators and investigators
• Verify investigator qualifications, training, resources, facilities, staff
• Verify data entry and maintain good documentation practices per SOPs, GCP and regulatory requirements
• Ensure enrollment of eligible subjects only
• Perform regulatory document review
• Manage device/product accountability and inventory
• Review adverse events and reporting accuracy
• Assess site recruitment and retention, provide improvement suggestions
• Complete monitoring reports and follow-up letters with findings and actions
• Maintain collaboration with international Medpace cross-functional teams

Skills

Fluent in Dutch

Fluent in English

Willing to travel 60-70%

Strong communication skills

Driver's license

Education

Bachelor of Science in Health or Life Science

Tools

Microsoft Office

Job description

Job Summary

The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Our successful Clinical Research Associates possess varied backgrounds in medical and other science‑related healthcare fields. Individuals who have succeeded in the CRA role include:

• Nurses
• Dieticians
• Pharmacists
• Biomedical researchers
• Pharmaceutical/Device Sales Representatives
• Biotech Engineers
• PhD/Pharm.D candidates
• ResearchCoordinators
• Research Nurses

PACE – MEDPACE CRA TRAINING PROGRAM

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence:

• PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
• PACE will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.

UNEXPECTED REWARDS

This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:

• Mid-sized CRO where you are not just a number
• Dynamic working environment, with varying responsibilities day-to-day
• Expansive experience in multiple therapeutic areas
• Work within a team of therapeutic, medical and regulatory experts
• Internally designed propriety Clinical Trial Management System – one stop shop for EDC, IWRS, regulatory portal, visits reports, and more
• Defined CRA promotion and growth ladder with potential for mentoring and management advancements
• Opportunity to work from home once job experience is gained
• Competitive pay

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement; and
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
• Maintain close collaboration, interaction, and effective working relationships with international Medpace internal cross-functional teams

Qualifications

• Minimum Bachelor of Science in Health or Life Science related field
• 1+ year of clinical research experience with direct patient-facing responsibility as a Clinical Research Coordinator, Clinical Study Coordinator or similar;
• Willing to travel approximately 60-70% nationally;
• Familiarity with Microsoft® Office;
• Fluent in Dutch and English is a must;
• Strong communication and presentation skills; and
• Valid driver’s license

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.