Junior Clinical Research Associate

Medpace; München; Vor Ort; EUR 45.000 - 75.000; Vollzeit

Zusammenfassung

An established industry player is seeking a Clinical Research Associate to embark on an exciting career in drug and medical device research. This role offers a unique opportunity to travel across Germany, Austria, and Switzerland while being part of a dedicated team focused on bringing innovative pharmaceuticals and medical devices to market. With comprehensive training provided, you will enhance your skills and gain invaluable experience in various therapeutic areas. If you have a passion for health sciences and wish to make a significant impact in clinical research, this position could be the perfect fit for you.

Leistungen

Competitive travel bonus

Flexible work hours

In-house travel agents

Ongoing therapeutic training

Opportunities to work with international teams

Competitive compensation and benefits package

Structured career paths for growth

Qualifikationen

• Minimum university degree in health/life science required.
• Proficient in Microsoft Office and detail-oriented.

Aufgaben

• Conduct qualification, initiation, monitoring, and closeout visits.
• Communicate with medical site staff and verify qualifications.
• Complete monitoring reports and ensure compliance.

Kenntnisse

Outstanding communication skills

Detail-oriented

Time management

Verbal and written communication in German and English

Ausbildung

University degree in health or life science

Tools

Microsoft Office

Jobbeschreibung

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. For those with medical and/or health/life science interest and background who want to explore the research field, travel throughout Germany, Austria, Switzerland, and be part of a team bringing pharmaceuticals 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.

PACE – MEDPACE CRA TRAINING PROGRAM

No clinical 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.
• To supplement your in-house and field-based training, you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

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

As a CRA, you will specifically be responsible for the following:

• Conduction of 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.

Qualifications

• Must have a minimum of a university degree in a health or life science related field;
• Approximately 60-80% travel;
• Proficient knowledge of Microsoft Office and general computer literacy;
• Outstanding communication and presentation skills;
• Must be detail-oriented and efficient in time management;
• Excellent verbal and written communication skills in German and English.

We kindly ask to submit your application in English.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

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

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Competitive compensation and benefits package
• Structured career paths with opportunities for professional growth

Awards

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.