Erika Wilder
Clinical Team Lead@ Atlantic Research Group
Los Angeles, California, United States
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Erika Wilder is a highly experienced professional with over 20 years of work experience in the pharmaceutical industry. She has a strong background in FDA regulations, regulatory affairs, and GMP. Erika has worked in various roles, including Senior CRA, Associate Director of Clinical Research Operations, and Regulatory Affairs Specialist. She is skilled in strategic planning, problem solving, scientific analysis, and process quality standards. Erika has also worked in the pharmaceutical industry, gaining expertise in product lifecycle management and electronic document management tools. She is currently based in Los Angeles, California.
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Emails and Phone Numbers

@endologix.com
@atlanticresearchgroup.com
+1 540213****
+1 631758****
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About

Responsible for study monitoring activities within a variety of rare disease therapies. Specialties: * Strategic/Tactical Planning * Problem Solving * Scientific Analysis * Process Quality Standards * Project Management * Product Lifecycle Management * Electronic Document Management Tools * Working knowledge of clinical development process * NIH/NCI Grants Policies and Compliance

Work Experience

2421 Ivy Road, Charlottesville, VA, 22903, US

Biotechnology Research

88
Phone
+1 5402130150
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Erika Wilder's Professional Milestones

  • Clinical Team Lead: Contributed to the development and success of a team and elevated their clinical team through strategic leadership.
  • Regulatory Affairs Specialist (2012-01-01~2014-01-01): Successfully navigated complex regulatory landscape, ensuring compliance and minimizing risk for a secure and trustworthy market.
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Education

California State University, Long Beach
California State University, Long Beach

Microbiology,

Bachelors,

Bachelor Of Science