Sad I/S Work Values

Daily Duties at Sad I/S:

Responsible for submission of applications for prolonged marketing approvals for a large range of drugs manufactured cross-country at the Hospital Pharmacies in Denmark. This important task included collection of pivotal documents, keeping track of multiple deadlines, strong management skills, an impeccable overview and close attention to detail. Provided responses to review letters issued by the Danish Medicine Agency as well as detailed responses to questions raised by medical professionals. The job also included review of PSUR's and Line listings. I consider myself knowledgeable in standard concept of the regulations, practices and procedures within the Regulatory affair field.

What they like about Sad I/S:

The social vibrance of a hiring firm is very important to you. Your ability to make and maintain friendships there is a critical part of your decision. You would likely be dissatisfied with a workplace that is quiet, cold, or otherwise not particularly social. When you investigate a new hiring company, ask recruiters, managers, and potential co-workers about the social life and opportunities there. This is especially important when you are relocating; moving dramatically alters your social sphere both inside and outside the workplace.

Tags

clinical research, medical affairs, Clinical research Associate, Clinical Research Assistant, Clinical Development Associate, Clinical Development Assistant, Regulatory Affairs Associate, Regulatory Affairs Assistant, Drug Safety Associate, Drug Safety Assistant, Clinical Development, Clinical Trials Associate, Clinical Trials Assistant

Skills

P&L responsibilities, Presentation, Ecommerce Strategy and digital marketing channels optimization - SEO, SEM, email, affiliates - for high-profile accounts., Technology Solutions, Sales Support, Software Implementation, Requirements Analysis & Specification, Leadership

These are some of the questions we asked our climbers about their experiences with Sad I/S: