We expanded our business from 1996 in APAC region.
We set up our China office in 2005!
In China, we already own over 300 employees in our office, the Regional Director of Clinical and, Post-marketing business
In order to expand our business, the preparation and approval of country related submission packages in accordance with ICH, GCP and all applicable regulations, laws and other guidelines and ethical standards – within specific timelines and quality standards, for the review and approval of site level critical documents for Investigational Product (IP) release in accordance with regulatory/sponsor requirements – within specific timelines and quality standards, we are hiring the Study Start-Up Associate role from level I to senior. The location can be Beijing, Shanghai or Guangzhou. If you are with the below skills and experience, please do not hesitate to share your resume with us.
- Bachelor or above degree in pharmacy, clinical;
- Be with the experience in clinical study initiation or start-up review at least 1 years;
- Knowledge on SOP, ICH-GCP;
- Good communication ability both in English and Mandarin;
- Site feasibility, EC submission is a plus.
Comparing with our competitors and pharmaceutical companies, we provide more flexible and reasonable working platform for coach and educate the new comer to be a professional person to concentrate on relevant industry. ICON also provides the good package and benefit to adapt the marketing development.
We more like a whole family with kind-heart and warm carefulness which you can balance your life and work here.
If you want to apply please send your resume to us directly: firstname.lastname@example.org . We are glad to respond you in time once received.
Welcome to consider and join ICON.