Raisa Echols Adams, M.S.

Raisa Echols Adams, M.S. Email and Phone Number

Regulatory Affairs and Compliance | Quality Assurance | Clinical Research Management @ ISK Biosciences Corporation
Raisa Echols Adams, M.S.'s Location
Greater Cleveland, United States
About Raisa Echols Adams, M.S.

With over six years of experience in clinical and non-clinical research, I am a Regulatory and Development Project Manager at ISK Biosciences Corporation, a leading provider of innovative and environmentally friendly solutions for the crop protection industry. I am passionate about leveraging my scientific and regulatory knowledge to ensure the safety, efficacy, and quality of our products and processes.I have a strong track record of managing complex regulatory projects, communicating effectively with internal and external stakeholders, and leading cross-functional teams to achieve compliance and quality objectives. I have also developed and implemented standard operating procedures, quality assurance measures, and data analysis methods to support research and development activities. My skills and credentials include a Master of Science in Medical Physiology, certification in Good Clinical Practices, and proficiency in data analysis and problem-solving. I am always eager to learn new things, collaborate with others, and contribute to the advancement of science and technology.

Raisa Echols Adams, M.S.'s Current Company Details
ISK Biosciences Corporation

Isk Biosciences Corporation

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Regulatory Affairs and Compliance | Quality Assurance | Clinical Research Management
Raisa Echols Adams, M.S. Work Experience Details
  • Isk Biosciences Corporation
    Regulatory And Development Project Manager
    Isk Biosciences Corporation Jul 2023 - Present
  • Case Western Reserve University School Of Medicine
    Clinical Research Associate
    Case Western Reserve University School Of Medicine Jun 2019 - Jun 2023
    Cleveland, Ohio, United States
    By maintaining certification and knowledge of Good Clinical Practices (GCPs) and Institutional Review Board (IRB) human subject re-search, develop Standard Operating Procedures (SOPs) for study workflows, participant consent, securing study participant personal in-formation, equipment usage, sample processing, and data analysis. Maintained GCP and IRB compliance by auditing informed consent forms, case report forms (CRFs), and appropriate deidentification of study data. Participate in developing novel treatments and diagnos-tics by managing and processing human biological samples. Sustained data security and privacy by overseeing database administration.
  • Baldwin Wallace University
    Neuroscience Lab Director
    Baldwin Wallace University May 2017 - Jan 2019
    Collaborated on the development, editing, and evaluation of IACUC and IRB proposals for continuing research proposals. Ensured compli-ance with animal use and care regulations by implementing quality assurance measures. Maintained drug and chemical use and storage records by ensuring EHS compliance. Effectively managed databases by streamlining data storage and retrieval. Implemented aseptic techniques to minimize contamination risks. Generated high-quality data and provided exceptional educational opportunities for neurosci-ence, histology, and molecular biology undergraduate students by planning, organizing, and executing various research projects.
  • Cognosante
    Assistant Team Lead
    Cognosante Sep 2013 - Aug 2015
    Cleveland
    Supported Affordable Care Act (ACA) and HIPAA compliance by training, coaching, and mentoring employees. Expanded knowledge of healthcare regulations and ACA by maintaining HHS Marketplace In-Person Assistor certification. Determined penetration rate at each site by maintaining and analyzing community outreach and daily productivity databases. Presented advisory sessions to address questions related to the ACA and enrollment process.
  • Xerox Services
    Compliance Junior Analyst
    Xerox Services Jan 2012 - Aug 2013
    Austin, Texas Area
    Conducted quality assurance research and data analysis by identifying root causes, leading to actionable insights. Assembled, scrutinized, and presented monthly performance metrics to management. Collected and evaluated escalation data to enhance and optimize business processes. Assessed compliance performance by creating monthly audit documentation for banking partners.
  • Sprint Pipeline Services
    Safety Administrator
    Sprint Pipeline Services Nov 2010 - Jun 2011
    Houston, Texas Area
    Functioned as a liaison between safety councils (HASC, CSC, Brazosport, ISTC), clients, and employees. Ensured personnel were assigned to appropriate job sites by performing pre-employment background checks, and ensuring updated safety, OQ, and DOT files for all active employees. Contributed to decreasing safety incidents from 6 to 1 with over one million quarterly man-hours reported by collaborating on the development and preparation for quarterly safety meetings.

Raisa Echols Adams, M.S. Education Details

Frequently Asked Questions about Raisa Echols Adams, M.S.

What company does Raisa Echols Adams, M.S. work for?

Raisa Echols Adams, M.S. works for Isk Biosciences Corporation

What is Raisa Echols Adams, M.S.'s role at the current company?

Raisa Echols Adams, M.S.'s current role is Regulatory Affairs and Compliance | Quality Assurance | Clinical Research Management.

What schools did Raisa Echols Adams, M.S. attend?

Raisa Echols Adams, M.S. attended Case Western Reserve University School Of Medicine, Baldwin Wallace University.

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