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ROLE SUMMARY The overall role of the Early Clinical Sciences (ECS) Clinician is to support the development and execution of one or more studies for small molecule and novel biological therapies from
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Quality Assurance, Medical Regulatory Compliance, R&D Legal, Corporate Compliance, Worldwide Safety & Regulatory and Pharmaceutical Sciences and other key study team members such as the Clinician, Clinical
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environment with a cross-functional clinical team. BASIC QUALIFICATIONS PhD in Pharmacokinetics, Clinical Pharmacology, Pharmacometrics, Engineering or PharmD Strong written and verbal communication skills
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degree, preferably in a life science discipline. BS/BA +5 years, MS/MA +3 years, PhD +0 year s of experience in medical writing or related field. Understanding of the role of each member of cross
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PhD in Pharmacometrics, Clinical Pharmacology, Pharmacokinetics, Engineering, Pharmaceutical Sciences, or PharmD Strong written and verbal communication skills PREFERRED QUALIFICATIONS Experience
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ROLE SUMMARY As a member of our Oncology team, you will play a critical role in supporting Translational Science Operations strategies, through scientific technical oversight and management
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advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply
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management as it relates to driving labeling process in regulated industry MS Office Suite; expert formatting skills (Word, XML) Bachelor's degree (in science or life sciences preferred) Attributes: Knowledge
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ROLE SUMMARY The Clinical Trial Transparency and Disclosure Manager (Senior Manager) is an integral member of the Medical Writing department. The role is responsible for preparing clinical
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Activation Partner, CTRO and Local Regulatory, Medical Affairs colleagues and other key stakeholders as required) Ensures compliance to relevant Global and Local, internal and external requirements and