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The HWSPH has focal areas of Biostatistics and Bioinformatics, Climate & Environmental Health, Community Health Services and Preventive Medicine, Epidemiology, Health Equity and Justice, Global Health, Health Behavior, Health Policy, Public Mental Health, and Technology & Precision Health and offers teaching and student mentoring opportunities in our BS in Public Health, MPH, PhD in Public Health (administered jointly with SDSU), and MS and PhD in Biostatistics degree programs.
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Master of Science (MSc) or PhD in Biostatistics, Psychometrics, or a relevant science such as Health Economics, Public Health, Epidemiology, Pharmacoeconomics, or Psychology.
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PhD in a quantitative subject e.g. Bioinformatics, Biostatistics, Computational Biology, Epidemiology with combined academic and or industry experience of 8+ years. GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organization where people can thrive.
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PhD or equivalent in Statistics, Biostatistics, Bioinformatics, Data Science, Epidemiology, Health Informatics, Computer Science or similar field. We are particularly interested in individuals who bring expertise in topics including Bayesian methods, causal inference, global drug surveillance, pharmacoepidemiology, biostatistics, data interoperability and harmonization, data standardization, surgical and medical device epidemiology, and health economics and outcomes research for quality measures.
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The project is led by Principal Investigator Dr. Sharelle Barber, Assistant Professor in the Department of Epidemiology and Biostatistics and Director of the Ubuntu Center on Racism, Global Movements & Population Health Equity at the Drexel University Dornsife School of Public Health (DSPH.
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Some of these services include clinical operations, project management, biostatistics, data management, regulatory affairs, medical affairs, and pharmacovigilance. E. Performing regulatory operations tasks including archiving/assembling/publishing regulatory filings and other health authority communications.
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Located on the Emory University campus, the School includes six academic departments and offers joint MPH degrees with the schools of medicine, nursing, business, law and theology and four additional PhD programs, in Epidemiology; Biostatistics, Behavioral, Social, and Health Education Science; Health Services and Health Policy; and Environmental Health Sciences.
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Other duties as assigned Qualifications MS in biostatistics, statistics, or PhD in biostatistics, statistics, epidemiology or related fieldAt least 4 years of related experience with MS or 1 year of related experience with PhD is expected but not required.
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MSc or PhD in Biostatistics or Psychometrics, or a relevant science, for example in Health economics, Public Health, Epidemiology, Pharmacoeconomics, or Psychology. OPEN Health is a flexible global organization that solves complex healthcare challenges across HEOR and market access, medical communications and creative omnichannel campaigns.
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ClinChoice is a global CRO that offers high-quality one-stop service to biopharmaceutical, medical device, and consumer products clients. Minimum of 3 years of work experience within the Medical Device or Pharmaceutical industry or 0-3 years with a PharmD/PhD. Strong communication, organizational, negotiation and interpersonal skills.
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H. Provides Regulatory Affairs support for internal and external quality system audits. G. Assists in development of best practices, work instructions for Regulatory Affairs processes and. Location: Jacksonville, FL or Irvine CA - 2 days per week - REMOTE FOR THE RIGHT CANDIDATE.
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E. Represents the regulatory affairs department in cross-functional project teams, plans and schedules regulatory deliverables to achieve project milestones. It has over 4,000 employees globally, with a strong and talented team, and a growing clinical operations presence in seven countries across Asia, North America, and Europe.
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General knowledge, understanding and application of principles, concepts and practices related to FDA regulations. F. Prepares associated product labeling to meet registration requirements for new or modified products; reviews product labeling associated with existing product to ensure compliance to regulatory requirements.
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D. Assisting in developing regulatory strategies for new product development initiatives. A. Reviewing/analyzing modifications to product, manufacturing process, packaging, etc. ClinChoice has established major delivery centers across the US, Canada, China, Europe, India, Japan, and the Philippines.
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Broad based technical knowledge and skills in diverse business functions (e.g., R&D, Operations, QA, laboratories, marketing, etc.) to determine impact of registration status of approved products and to determine appropriate regulatory pathway.
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