Job Summary Work with the company executives located in multiple offices to provide executive and general administrative support, including travel, calendar management, company event and meeting planning, taking minutes and financial documentation. Act as primary administrative support for the SSF office including but not limited to general management of the
October 3, 2019 SALT LAKE CITY, USA. Elevar Therapeutics and Abu Dhabi-based Neopharma have entered into an agreement to establish a joint venture in the United Arab Emirates. The 50:50 venture is planned to undertake a broad range of development and commercialization activities for rivoceranib in the Middle East, North
September 20, 2019 SALT LAKE CITY, USA. Elevar Therapeutics announced that data from the ANGEL trial has been accepted for a podium presentation by the European Society for Professional Oncology at the annual meeting in Barcelona, Spain. The ANGEL trial is a randomized phase 3 study of rivoceranib (commonly known
SALT LAKE CITY, USA, July 23, 2019 LSK BioPharma is pleased to announce the addition of one new member to the Board of Directors: Wook Kim. He is currently a Managing Director of HLB and Next Science, a Korea-based company. He has over 20 years’ experience
Business Development/Safety Project Management Associate. Work within the pharmaceutical industry practices and standards for new drug development and safety reporting. Organize aggregate safety data including adverse events, concomitant medications and lab data. Prepare and lead safety oversight meetings for global phase III trials and study
Overview We are currently seeking a full-time, San Francisco office-based CMC Senior Director to join LSK BioPharma. This position will manage and guide our API and CMC activities for our small molecule drug substance and product programs from preclinical through commercial. If you want an exciting career
Position has been filled. Responsibilities and Duties Essential Duties & Responsibilities: Primary contact for the site, supervise and monitor clinical trials to ensure adherence to ICH-GCP standards, study protocol, SOPs and regulations. Ensure proper adherence to protocol, Informed consent procedures, source data verification, compliance to safety