Regulatory Submissions Coordinator

vor 2 Wochen

München, Deutschland Medpace, Inc. Vollzeit

Job Summary:
Our clinical operations activities are growing rapidly, and we are currently seeking a full-time** office-based** Regulatory Submissions Coordinator to join our Clinical Operations team in **Munich**. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

**Entry-level positions with permanent contract are available for recent graduates.**

Responsibilities:

- Communicate with research sites in Germany, Austria and Switzerland (hospitals, etc.) to collect all essential documents required before the site starts to enroll patients to participate in the clinical trial;
- Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration;
- Ensure submissions comply with applicable regulations and guidance documents;
- Advise on changing country regulations and compliance requirements; and
- Track submissions and ensure timely filing of documents.

Qualifications:

- Bachelor's degree (preferably in a Life Sciences field);
- Interest in drug development and clinical trials;
- Full professional proficiency in German and English in written and verbal communication;
- Knowledge of Microsoft® Office; and
- Excellent organization and communication skills, great attention to detail.

**Travel**: None

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**
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives

**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.

  • Experienced Regulatory Submissions

    vor 1 Woche

    München, Deutschland Medpace Vollzeit

    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...

  • Specialist, Regulatory

    vor 4 Wochen

    München, Deutschland Medpace Vollzeit

    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. Our clinical operations...

  • Study Coordinator Clinical Research

    vor 2 Wochen

    München, Deutschland Medpace Vollzeit

    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. As a...

  • Regulatory Affairs Manager

    Vor 5 Tagen

    München, Deutschland Cpl Life Sciences Vollzeit

    ob Title: European Regulatory Affairs Manager Location: Munich, Germany - Hybrid, 3x a week in the office Remuneration: Competitive salary and package Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is looking for a...

  • Regulatory Officer

    vor 3 Wochen

    München, Deutschland PSI CRO Deutschland GmbH Vollzeit

    Company DescriptionPSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Regulatory Officer Munich, Germany I Full-time Job DescriptionJoin...

  • Clinical Trial Coordinator

    vor 21 Stunden

    München, Deutschland Alira Health Vollzeit

    Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description...

  • Regulatory Officer

    vor 4 Wochen

    München, Deutschland PSI CRO Deutschland GmbH Vollzeit

    Company Description PSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Regulatory OfficerMunich, Germany I Full-time Job Description Join...

  • Regulatory Officer

    vor 3 Wochen

    München, Deutschland PSI CRO Deutschland GmbH Vollzeit

    Company Description PSI is a leading Contract Research Organization with almost 30 years on the market, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Regulatory Officer Munich, Germany I Full-time Job Description Join...

  • Senior Manager/Director of Regulatory Affairs

    Vor 5 Tagen

    München, Deutschland Cpl Life Sciences Vollzeit

    ob Title: European Regulatory Affairs Manager Location: Munich, Germany - Hybrid, 3x a week in the office Remuneration: Competitive salary and package Regulatory Affairs Manager opportunity working for an established pharmaceutical company that specialises in generic, OTC, and prescription medicines. The business is increasingly growing and is...

  • Clinical Trial Coordinator

    Vor 3 Tagen

    München, Deutschland Alira Health Vollzeit

    Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others. Job Description...