Regulatory Submissions Coordinator

We are looking for a Regulatory Submissions Coordinator for our office in Rehovot, Israel.

• Quality check on submission documents and site essential documents;
• Interaction with US Central IRBs, sites and international associates;
• Preparation and approval of informed consent forms; and
• Review pertinent regulations to develop proactive solutions to start-up issues and challenges.

• A Bachelor's degree in a relevant field;
• 1 - 3 years of job experience in a clinical trial environment;
• Knowledge of local regulations regarding clinical studies and the conduct of such studies;
• Strong oral and written communication skills; and
• Excellent computer skills, including a working knowledge of Microsoft Office applications.

Travel: Minimal

WHY MEDPACE?

At Medpace, you will find work that is both challenging and rewarding. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally.

WHAT TO EXPECT NEXT

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

EO/AA Employer M/F/Disability/Vets