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withstanding regulatory scrutiny. This position will focus primarily in Trial Master File Operations. Facilitate the execution of the TMF Operations' activities to enable complete, compliant and consistent study
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tools, both CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection systems Ensure the required study-specific CDS documents in the Trial Master File (TMF) are of high
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tools, both CRF and non-CRF, using an electronic data capture (EDC) system and/or other data collection systems. Ensure the required study-specific CDS documents in the Trial Master File (TMF) are of high
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with 8 years of experience OR a bachelors with at least 5 years of experience OR Masters Degree with more than 3 years of experience, OR a PhD with 0+ years of experience. 5+ years of demonstrated
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distilling complex analysis and concepts into concise business-focused takeaways. QUALIFICATIONS: • Bachelor's degree with 7+ years of experience OR Masters Degree with 6+ years of experience OR PhD with 2
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first in human (FIH) through proof of concept (PoC) studies, including proof of mechanism (PoM) and early signals of efficacy (ESoE) studies in a given therapeutic area. The primary therapeutic areas
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interpersonal and communication skills Ability to plan, organize, prioritize, and execute multiple tasks within assigned objectives Proficiency with computer applications (MS Office) Nice-to-Have Master's degree
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Job Description JOB SUMMARY The Site Care Partner is the main Pfizer point of contact for investigative sites as well as accountable for safeguarding the quality and patient safety
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projects to expand and maintain the system. Collaborating with the Infrastructure lead on strategy, methodologies, master planning and documentation of the PI data historian to align with industry best
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POSITION SUMMARY You will join a team of scientists supporting oncology development programs. You will be the primary Clinical Pharmacology Lead providing clinical pharmacology expertise to a