Clinical Research Coordinator- Clinical Research Associate Home-Based

Medpace, Inc.; Deutschland; Hybrid; EUR 45.000 - 80.000; Vollzeit

Zusammenfassung

An established industry player seeks passionate Clinical Research Associates to join their dynamic team. This role offers the chance to enhance pharmaceuticals and medical devices while receiving comprehensive training through the PACE Program. Enjoy a flexible work environment, competitive pay, and significant travel bonuses as you conduct vital research across the DACH region. With opportunities for career advancement and ongoing training from medical experts, you will play a crucial role in improving lives through innovative clinical research. If you are ready to make a difference, this is the perfect opportunity for you!

Leistungen

Competitive travel bonus

Flexible work hours

In-house travel agents

Ongoing therapeutic training

Employee appreciation events

Generous PTO packages

Health and wellness initiatives

Structured career growth opportunities

Qualifikationen

• Minimum 1 year of experience as a Clinical Research Coordinator.
• Proficient in Microsoft Office and strong communication skills.

Aufgaben

• Conduct qualification, initiation, monitoring, and closeout visits at research sites.
• Verify investigator qualifications and ensure compliance with protocols.
• Perform on-site and remote monitoring activities using Clinical Trial Management System.

Kenntnisse

Clinical Research Coordination

Microsoft Office

Communication Skills

Attention to Detail

Time Management

Fluency in German

Fluency in English

Ausbildung

Bachelor's degree in health or science-related field

Jobbeschreibung

Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team!

This is an exciting opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research Associate (CRA) openings with Medpace. Through our PACE Training Program, you will receive the training needed to become a fully functional CRA with the opportunity to work home-based. You will also have the opportunity to earn a generous travel bonus in addition to a competitive salary.

UNEXPECTED REWARDS:

This role 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 opportunity for significant travel bonus.

CRA PERKS:

• Competitive travel bonus
• Flexible work hours across days within a week
• In-house travel agents
• Ongoing therapeutic training by our in-house physicians who are medical and regulatory experts
• Opportunities to work with an international team of CRAs

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
• Communicate with the medical site staff including coordinators, clinical research physicians, and their site staff;
• Verify investigator qualifications, training, resources, facilities, laboratories, equipment, and staff;
• Verify medical records and source documentation against case report forms, ensure good documentation practices, and communicate protocol deviations as per SOPs, GCP, and regulations;
• Perform on-site and remote monitoring activities with a risk-based approach using our Clinical Trial Management System;
• Ensure enrollment of only eligible subjects;
• Review regulatory documents;
• Manage medical device and investigational product/drug accountability and inventory;
• Review adverse events, serious adverse events, medications, and illnesses for accurate data reporting;
• Assess patient recruitment and retention strategies and suggest improvements;
• Complete monitoring reports and follow-up letters summarizing findings and recommended actions.

Qualifications

• Bachelor's degree in health or science-related field;
• Minimum 1 year of experience as a Clinical Research Coordinator;
• Ability to travel 60-70% within the DACH region, with some remote visits;
• Proficient in Microsoft Office;
• Strong communication and presentation skills;
• Attention to detail and efficient time management;
• Fluency in German and English, both verbal and written.

#LI-Remote

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV services to the biotech, pharma, and medical device industries. Our mission is to accelerate the development of safe and effective therapeutics globally, leveraging local expertise across key therapeutic areas including oncology, cardiology, metabolic disease, and more. Headquartered in Cincinnati, Ohio, with over 5,000 employees across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

Our work over the past 30+ years has positively impacted countless lives. Today, we continue to improve the lives of those living with disease and illness.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits
• Generous PTO packages
• Structured career growth opportunities
• Employee appreciation events
• Health and wellness initiatives

Awards

• Forbes' America's Most Successful Midsize Companies (2021-2024)
• CRO Leadership Awards from Life Science Leader magazine

What to Expect Next

A Medpace team member will review your qualifications and contact you with next steps if interested.

EO/AA Employer M/F/Disability/Vets