Senior Regulatory Submissions (Start-Up) Coordinator - UK

Recruiter
Medpace
Location
London (Greater)
Posted
10 Oct 2018
Closes
15 Oct 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Senior Regulatory Submissions (Start-Up) Coordinator - UK

Permanent

Location: Central London or Stirling (Scotland)

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 2,500 people across 35 countries.



Our clinical activities are growing rapidly, and we are currently seeking a full-time, office-based Senior 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.

Responsibilities


Prepare, review, and file clinical trial applications to domestic and international regulatory agencies;
Ensure submissions comply with applicable regulations and guidance documents;
Advise sponsors on changing regulations and compliance requirements; and
Track submissions and ensure timely filing of documents.


Qualifications


Bachelor's degree in life sciences;
Previous experience as a Regulatory Submissions Coordinator in a Clinical Research setting;
Excellent organization and communication skills;
Knowledge of Microsoft® Office; and
Hands-on experience preparing, reviewing, and submitting regulatory documentation;


Travel: Minimal



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


Winner of the ACRP-Avoca CRO Quality Award in 2018
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.



EO/AA Employer M/F/Disability/Vets



*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 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.

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