Author: ETadmin

Job Title Manager, Quality Assurance   Job Status Full Time   Job Summary The Manager of Quality Assurance position is responsible for oversite of the Quality Management System (QMS). This position provides support and guidance to ensure compliance with regulatory requirements as well as maintain and

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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

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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

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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

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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

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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

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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.

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