Entry Level - Clinical Research Associate

Medpace, Inc.; København; On-site; DKK 450,000 - 700,000; Full time

Benefits offered by this job

Competitive compensation

Health & retirement benefits

Office-based culture with occasional W

Company-sponsored social events

Job summary

Medpace, Inc. is seeking a Clinical Research Associate to join our Copenhagen team for the CRA training program and initial office-based work with future hybrid/home-based options. The role requires Danish language proficiency and the ability to travel nationally, about 60–80% of the time.

Candidates from medical or health/life science backgrounds are welcome; the program aims to develop high-functioning Medpace CRAs through hands-on exercises and mentoring.

Qualifications

• Bachelor degree in health or life science; field preferred.
• Fluency in Danish is required.
• Willing to travel 60–80% nationally.
• Must hold a valid driver’s license.
• Office-based during the core training program.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites.
• Communicate with 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 source documentation verification against case report form data and informing the site staff of errors and deviations per SOPs, GCP and regulations.
• Verification that the investigator is enrolling only eligible subjects.
• Regulatory document review.
• Medical device/investigational product/drug accountability and inventory.
• Review adverse events and data reporting per protocol.
• Assess site recruitment and retention performance and suggest improvements.
• Complete monitoring reports and follow-up letters with significant findings and actions.

Skills

Danish language fluency

Strong communication skills

Presentation skills

Education

Bachelor's degree in health or life science

Tools

Microsoft Office

Job description

Job Summary

The Clinical Research Associate role 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, travel Denmark, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you! Please note that to take full advantage of the training on offer, you must be within commuting distance of our Medpace Copenhagen office as this role is initially fully office based with hybrid and home-based opportunities in the future. Fluency in local language and English are required.

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
• Pharmacy Technicians
• Pharmaceutical/Device Sales Representatives
• Biotech Engineers
• PhD/Pharm.D candidates
• Health and Wellness Coordinators
• Site Coordinators, Clinical Research Coordinators
• Research Assistants.

PACE® – MEDPACE CRA TRAINING PROGRAM

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:

• Dynamic working environment, with varying responsibilities day-to-day
• Expansive experience in multiple therapeutic areas
• Work within a team of therapeutic and regulatory experts
• Defined CRA promotion and growth ladder with potential for mentoring and management advancements
• Competitive pay and bonus program

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;
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

Qualifications

• Minimum of a bachelor’s degree; Health or life science related field preferred;
• Working proficiency/fluency in Danish language;
• Willing to travel approximately 60-80% nationally;
• Familiarity with Microsoft® Office; and
• Strong communication and presentation skills a plus.
• Must hold a valid drivers licence
• Willing to be fully office based during the core training program.

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.