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Durham, North Carolina
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clear and concise clinical submission documents, including clinical study reports, protocols, clinical ... Job Overview:
As a Lead Medical Writer on most types of writing projects. You will
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Seoul,
South Korea
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education.
• Familiarity with the structural and content requirements of clinical study reports ... .
• Serves as a Lead Medical Writer for late phase studies of Real-World Solutions team. Prepares assigned
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Quebec City,
Canada
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correspondence; Ensures timely transmission of clinical data with study site and technical reports as requested ... ; coordinates correspondence; Ensures timely transmission of clinical data with study site and technical reports
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Rwanda
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as needed.
• Authors protocols, reports, and other study documents with independent, critical ... the full spectrum of study designs that may be applicable for global health actors, which include but
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Accra,
Ghana
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as needed.
• Authors protocols, reports, and other study documents with independent, critical ... the full spectrum of study designs that may be applicable for global health actors, which include but
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Nairobi,
Kenya
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as needed.
• Authors protocols, reports, and other study documents with independent, critical ... the full spectrum of study designs that may be applicable for global health actors, which include but
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Reading,
United Kingdom
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as needed.
• Authors protocols, reports, and other study documents with independent, critical ... the full spectrum of study designs that may be applicable for global health actors, which include but
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North Sydney,
Australia
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(in the role of project manager, with oversight from senior team members)
Develop key study deliverables, including protocols, data collection tools, study reports and publications (e.g., posters
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Melbourne,
Australia
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(in the role of project manager, with oversight from senior team members)
Develop key study deliverables, including protocols, data collection tools, study reports and publications (e.g., posters
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Montreal,
Canada
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correspondence; Ensures timely transmission of clinical data with study site and technical reports as requested ... ; coordinates correspondence; Ensures timely transmission of clinical data with study site and technical reports
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San Antonio, Texas
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Safeguards the wellbeing of research subjects in a medical capacity; reviews study protocols; plans and ... escalates study issues; clarifies protocols, inclusion/exclusion and research subject eligibility
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Livingston,
United Kingdom
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pathology interpretations. Monitor progress of studies under purview and inform senior staff of any problems ... laboratory information.
Report results in accordance to protocols mandated by the regulatory
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Kanata, Ontario
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Clinical Research Associate, the Study Analyst works the full continuum of the study, from start up ... or clinical trial support role in an academic or hospital setting
A study or clinical trial
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Mississauga, Ontario
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Clinical Research Associate, the Study Analyst works the full continuum of the study, from start up ... or clinical trial support role in an academic or hospital setting
A study or clinical trial
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Quebec,
Canada
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Clinical Research Associate, the Study Analyst works the full continuum of the study, from start up ... or clinical trial support role in an academic or hospital setting
A study or clinical trial
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