Job Title Regulatory Affairs – Senior Manager Job Status Full Time Job Summary We are currently seeking a full-time, office-based Regulatory Affairs Senior Manager to join LSK BioPharma. This position will work with our clinical and product development teams to contribute to the preparation of regulatory submissions for our
Job Title Senior Manager Clinical, Quality Assurance (CQA) Job Status Full Time Job mmary Responsible for ensuring clinical processes within the Drug Development Group are conducted in accordance with corporate SOPs, guidelines and regulations. Develops, performs, and manages clinical quality assurance activities. Presides over clinical audits. Job Details Ensure that
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
Job Title Clinical Trial Manager (CTM) Job Status Full Time Job Summary The Clinical Trial Manager (CTM) manages at least one primary project, and depending on scope and phase of project, may support multiple projects. The CTM provides project management expertise throughout the development and implementation
SALT LAKE CITY, USA, June 30, 2019 LSK BioPharma (or “LSKB”), a US-based biopharmaceutical firm and Jiangsu Hengrui Medicine, Co., Ltd. (SHA:600276, or “Hengrui”), one of the largest and most innovative fully-integrated biopharmaceutical companies based in China, today announced the first patient has been enrolled in
LSK BioPharma Announces Preliminary Review of Top-Line Results from ANGEL Study SALT LAKE CITY, USA, June 27, 2019 – LSK BioPharma (LSKB) has completed the unblinding and preliminary review of topline data from its ANGEL Study, a Phase III clinical trial for rivoceranib (apatinib) which enrolled 460
Job Title Clinical Trial Associate (CTA) Job Status Full Time Job Summary The Clinical Trial Associate (CTA) supports at least one primary project, and depending on scope and phase of project, may support multiple projects. The CTA provides support to one or more Clinical Trial Managers (CTM). Interacts with
Job Title Senior Scientists, Clinical Job Status Full Time Job Summary The senior clinical scientist will be a key player of a multi-disciplinary, matrix team ensuring that scientific issues are appropriately considered with respect to highly complex clinical data findings. This individual has the responsibility for influencing
Job Title Principal Medical Writer Job Status Full Time Job Summary The Principal Medical Writer is responsible for authoring documents, including clinical study reports (CSRs), protocols, investigator’s brochures, publications and other documents. This position is also expected to contribute to higher level submission documents. This position will be responsible
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