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Home based - Regulatory Submissions Coordinator in Santiago de Chile | Careers at Chile, Santiago de Chile Skip to Main Content Please Enable Cookies to Continue Please enable cookies in your browser to experience all the personalized features of this site, including the ability to apply for a job. Welcome page Welcome page Returning Candidate? Log back in!
Home based - Regulatory Submissions Coordinator
Job Locations Chile-Santiago de Chile Category Clinical Operations
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.
As a Regulatory Submissions Coordinatoryou 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 Regulatory Submissions Coordinators, you will gain valuable hands on experience to enable you to develop a career in clinical research.
Provide day-to-day departmental/project support activities, such as collection of vital documents for ethics submissions and preparation of study documents to competent authorities; Support Regulatory Submission Managers and Start Up teams in ensuring deadlines are adhered to; Conduct quality control of documents; Maintain spreadsheets and compile reports; and Provide advice and guidance to internal and external team members to ensure compliance with applicable regulations and requirements; Perform other tasks as needed.
Bachelor's degree is required (preferably in a Life Sciences field); At least 3 - 4 years of regulatory submissions experience; 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.
We kindly ask to submit applications in English.
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.
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.
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 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.
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