Jobbörse

Junior Clinical Research Associate - Clinical Study Coordinator Experience Required

Veröffentlicht am 15. Okt. 2026

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Medpace Germany GmbH

Hamburg

EnglischJuniorDeutsch B1–B2

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Gehalt in der Anzeige

43.000 € bis 61.000 €

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Introduction

Job Summary : For Clinical Study Coordinators located in Hamburg: 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. For those with a Life Sciencedegree with clinical research experience who want to travel throughout Germany, Austria, Switzerland and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

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.

Responsibilities :

Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol;
Communication with the medical site staff including coordinators, clinical research physicians, and their site staff;
Verify 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;

On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward;

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;

Assess 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.

Must have a minimum of a Bachelor’s degree in a health or science related field;
Experience as a Clinical Research Coordinator (minimum 1 year);
Ability to travel 60-70% to locations in the DACH region;
Proficient knowledge of Microsoft® Office;
Must be detail-oriented and efficient in time management
Excellent verbal and written communication and presentation skills in German and English.

PACE – MEDPACE CRA TRAINING PROGRAM

Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.

Through our PACE Training Program, you will join other P rofessionals A chieving C RA E xcellence:

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.

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.

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 international team of CRAs

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.

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.

We kindly ask to submit your application in English. Please note that this role is fully remote-based.

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.

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Eckdaten der Stelle

Arbeitgeber: Medpace Germany GmbH
Position: Junior Clinical Research Associate - Clinical Study Coordinator Experience Required
Stadt: Hamburg
Arbeitsmodell: nicht angegeben
Sprache: Englisch
Erfahrungsstufe: Junior
Veröffentlicht: 15. Okt. 2026
Quelle: StepStone

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Junior Clinical Research Associate - Clinical Study Coordinator Experience Required

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Responsibilities :

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Eckdaten der Stelle

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