Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Junior Regulatory Submissions Specialist (Study Start up)

Company: Medpace
Location:
Reference: DERSC1118
Closing Date: 23 Dec 18
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

Junior Regulatory Submissions Specialist (Study Start up) required to join Medpace team in Munich, Germany

Requirements:

Junior Regulatory Submissions Specialist (Study Start up)

Location: Munich, Germany

Overview

Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach. We leverage local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 2,700 people across 36 countries.

Job Summary

Our European activities are growing rapidly, and we are currently seeking a full-time, office-based Junior Regulatory Submissions Coordinator to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. 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.

 

Ours is a culture of expertise, and we empower our teams to employ their unique talents and experience to take an assertive approach to research, problem solving, and ultimately supporting our partners. At Medpace our employees embody our values and our approach to serving our clients. They work hard, understand our high expectations, and rise to the challenge. In return they are rewarded with interesting projects, career advancement, and recognition and exposure to our international footprint. These are just a few reasons talented individuals join the Medpace team.

 

As a Junior Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team, and will be mentored and supported as you develop your skills. Working directly with other Regulatory Submissions Coordinators and Managers, you will gain valuable hands on experience to enable you to develop a career in clinical research.

Responsibilities

  • Provide day-to-day departmental/project support activities, in support of ethics submission and competent authority clinical trial applications
  • Support Regulatory Submission Coordinators and Start-Up teams in ensuring deadlines are adhered to;
  • Conduct quality control of documents;
  • Maintain spreadsheets and compile reports; and
  • Perform other tasks as needed.

Qualifications

  • A minimum of a Bachelor's degree is required (preferably in a Life Sciences field);
  • Some experience in an office setting is preferred;
  • Excellent organizational and prioritization skills;
  • Knowledge of Microsoft Office;
  • Great attention to detail and excellent oral and written communication skills; and
  • Fluency in spoken and written English and German.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities. 

 

Awards

  • Medpace Named a Top Cincinnati Workplace for 2015, 2016, 2017 and 2018 by the Cincinnati Enquirer
  • Winner of the ACRP-Avoca CRO Quality Award in 2018
  • Recognized with six CRO Leadership Awards from Life Science Leader magazine
  • Eagle Award winner - which recognizes outstanding leadership, professionalism, integrity, and dedication to advancing the clinical research profession through strong site partnerships

 

What to Expect Next

We look forward to receiving your application.  A member of our recruitment team will review your qualifications and if interested, you will be contacted for an interview.

 

Apply for this job: Junior Regulatory Submissions Specialist (Study Start up)

Contact Information:

Address:  Medpace Germany GmbH
Theresienhoehe 30 80339 München Germany
80339
Germany
Tel:  +49 (0) 89 89 55 718 0
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.