You may already know Covance as the leading Central Laboratory services provider, but did you know we are one of the most stable, fastest growing global Contract Research Organization? For example, our Clinical Development teams have supported the development of 11 out of the 16 new medicines approved by the FDA in 2013… And in spite of being one of the Top 3 global CRO, we still have a personal touch to every single employee. The work we do at Covance impact the lives of millions of people around the world… so you could too as our next There is a method to navigate the challenging regulatory waters, and we at Covance are expert sailors. So if you have at least 2 years work experience in a Start-up role in a CRO, Bio or Pharmaceutical company, with a strong working knowledge of Submissions, the ICH guidelines, FDA and IEC regulations, do not hesitate to explore the career opportunities of one of the market leaders. These are also excellent opportunities for CRAs who are looking for a home based / no travel role. Location: home-based, across The Netherlands. You will join our Global Site Services Division. Global Site Services (GSS) is our Regulatory/ Study start-up team responsible for processing submissions for the Ethics Committees and liaising with local regulators. Among others, your main responsibilities will include: Collecting, reviewing, approving process and track regulatory & investigator documents required for study site activation Preparing new investigator submission packages to Local and/ or Central IRB /IEC in Belgium and the Netherlands Negotiating contracts and budgets with investigative sites within parameters provided by Sponsor Liaising with operational project team regarding project issues (i.e., participate in team meetings) Establishing, conducting and maintaining relevant QC processes in regards Feasibility Assessments Conduct QC of feasibility documents as required by the process To learn more and apply, please visit www.covancecareers.com and search for the reference 42014, or follow the link: http://jobsearch.covance.com/jobs/889314-Start-up-Specialist.aspx Don´t assume all companies will bring you the same! Job titles may be similar, but the content of your work day is what counts. So think for a second on the working environment of a company capable of contributing to the development of : 50% of the latest breakthrough oncology treatments The top 25 currently marketed medicines And being ranked the 4th World's Most Admired Health Care Pharmacy Company in 2012. As we are a truly global, we can offer you international career development. As we are a full-service CRO, our structure allows the development of a varied career, touching different angles of the Drug Development Process in the same company. And we proud ourselves to have a team of dedicated managers, who will be at your side to make the most of your career with us. To initiate a confidential conversation with Covance, do not hesitate to contact Carlos Villanueva at (U dient eerst in te loggen, voordat u dit email adres kunt zien)
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Vast contract, bepaalde tijd, Vast contract, onbepaalde tijd uur per week