Jetzt als Entry Level - Regulatory Submissions Coordinator bei Medpace Inc in München bewerben – Deine Chance!

• Prepare, review, and file clinical trial applications for Germany;
• Communicate with research sites in Germany (hospitals, etc.) to collect all essential documents required before the site starts to enrol 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.

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

Perks:

• Flexible work hours
• WFH opportunities - Hybrid model
• Career development
• Annual salary review
• Meal vouchers
• Working environment: join a motivated team in our new offices in central Munich near Bavaria Park.

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  WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.