May 2019

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

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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

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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

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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

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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

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