Drug Safety/Medical Information Specialist jobs in Pine Bluff, AR

Drug Safety/Medical Information Specialist is responsible for collecting, monitoring, processing, and distributing adverse event reports and information queries for investigational and marketed products. Reviews safety and medical information for the assigned products, including safety components of protocols and studies for assigned drugs. Being a Drug Safety/Medical Information Specialist may require a bachelor's degree in area of specialty. Typically reports to a supervisor or manager. To be a Drug Safety/Medical Information Specialist typically requires 0-2 years of related experience. Works on projects/matters of limited complexity in a support role. Work is closely managed. (Copyright 2024 Salary.com)

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Research Participation Opportunities at the U.S. Food and Drug Administration - NCTR General 2024
  • U.S. Food and Drug Administration (FDA)
  • Jefferson, AR FULL_TIME
  • Description

    The Oak Ridge Institute for Science and Education (ORISE) Research Participation Programs at the U.S. Food and Drug Administration (FDA) are educational and training programs designed to provide undergraduate and graduate students, post-master and post-doctoral, and faculty opportunities to participate in project-specific research and developmental activities at the National Center for Toxicological Research (NCTR). The FDA is responsible for protecting the public health by ensuring the safety, efficacy, and security of human and veterinary drugs, biological products, and medical devices; and by ensuring the safety of our nation’s food supply, cosmetics, and products that emit radiation.  The mission of NCTR is to conduct scientific research to develop and support innovative tools and evaluation of approaches that FDA uses to protect and promote individual and public health.  To accomplish its mission, NCTR has established three strategic goals to ensure the conduct of innovative regulatory-science research vital to FDA.  Regulatory Science-the science of developing and establishing tools, standards, and approaches to assess the safety, efficacy, quality, and performance of regulated products-is the foundation of decision-making at FDA.  The three strategic goals are:

    • Advance scientific approaches and tools required to support public health
    • Promote global interactions in regulatory science research
    • Improve administrative management and develop new communication materials and methods to support HHS/FDA science goals

    This is an open announcement to collect applicants for future research opportunities.  The opportunities include full-time, part-time, and summer appointments at NCTR. Contact ORISE.FDA.NCTR@orau.org for more information.

    This program, administered by ORAU through its contract with the U.S. Department of Energy to manage the Oak Ridge Institute for Science and Education, was established through an interagency agreement between DOE and FDA. Appointments can vary from a few months to one year, but may be renewed for up to three years upon recommendation of FDA, contingent on the availability of funds. The participant will receive a monthly stipend commensurate with educational level and experience. Proof of health insurance is required for participation in this program. Participants do not become employees of FDA, DOE or the program administrator, and there are no employment-related benefits.

    See https://orise.orau.gov/fda/ or http://www.fda.gov/ for more information.

    Completion of a successful background investigation by the Office of Personnel Management is required for an applicant to be on-boarded at FDA.  OPM can complete a background investigation only for individuals, including non-US Citizens, who have resided in the US for a total of three of the past five years.

    FDA Ethics Requirements

    If an ORISE Fellow, to include their spouse and minor children, reports what is identified as a Significantly Regulated Organization (SRO) or prohibited investment fund financial interest in any amount, or a relationship with an SRO, except for spousal employment with an SRO, and the individual will not voluntarily divest the financial interest or terminate the relationship, then the individual is not placed at FDA.   For additional requirements, see FDA Ethics for Nonemployee Scientists.

    FDA requires ORISE participants to read and sign their FDA Education and Training Agreement within 30 days of his/her start date, setting forth the conditions and expectations for his/her educational appointment at the agency.  This agreement covers such topics as the following:

    • Non-employee nature of the ORISE appointment;
    • Prohibition on ORISE Fellows performing inherently governmental functions;
    • Obligation of ORISE Fellows to convey all necessary rights to the FDA regarding intellectual property conceived or first reduced to practice during their fellowship;
    • The fact that research materials and laboratory notebooks are the property of the FDA;
    • ORISE fellow’s obligation to protect and not to further disclose or use non-public information.
  • 30 Days Ago

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Research Biologist
  • US Food and Drug Administration
  • Jefferson, AR FULL_TIME
  • Duties Knowledge of nanomaterial and research projects as they relate to the Nanocore’s overall mission in support of the regulatory mission of the agency. Keeps current with scientific literature, su...
  • 15 Days Ago

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Microbiologist
  • US Food and Drug Administration
  • Jefferson, AR FULL_TIME
  • Duties Performs the full range of microbiology on a variety of samples, including the difficult, complex or unusual samples submitted by agency personnel about regulatory monitoring and enforcement ac...
  • 29 Days Ago

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FDA Postdoctoral Research Fellowship in Genetic Toxicology
  • U.S. Food and Drug Administration (FDA)
  • Jefferson, AR FULL_TIME
  • Description *Applications will be reviewed on a rolling-basis. FDA Office and Location: A postdoctoral fellowship opportunity is currently available in the Division of Genetic and Molecular Toxicology...
  • Just Posted

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FDA Postdoctoral Research Fellowship in Neurotoxicology
  • U.S. Food and Drug Administration (FDA)
  • Jefferson, AR FULL_TIME
  • Description *Applications will be reviewed on a rolling-basis. FDA Office and Location: A postdoctoral fellowship opportunity is currently available in the Division of Neurotoxicology at the National ...
  • 1 Day Ago

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FDA Nanotechnology Postdoctoral Research Fellowship
  • U.S. Food and Drug Administration (FDA)
  • Jefferson, AR FULL_TIME
  • Description *Applications will be reviewed on a rolling basis. FDA Office and Location: A postdoctoral fellowship opportunity is currently available in the Division of Neurotoxicology at the National ...
  • 8 Days Ago

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0 Drug Safety/Medical Information Specialist jobs found in Pine Bluff, AR area

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FT Data Entry Specialist - Work From Home>
  • Sharecare
  • Pine Bluff, AR
  • [Administrative Assistant / Remote] - Anywhere in U.S. / Competitive pay - As a Data Entry Specialist you'll: Access var...
  • 4/25/2024 12:00:00 AM

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Patent Engineer
  • Snap Inc.
  • Little Rock, AR
  • Snap Inc is a technology company. We believe the camera presents the greatest opportunity to improve the way people live...
  • 4/24/2024 12:00:00 AM

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AR/Billing Specialist I
  • Mercy Flights Ground & Air
  • Little Rock, AR
  • Description:Mercy Flights is accepting applications for a Full-Time AR/Medical Billing Specialist I.We are looking for t...
  • 4/24/2024 12:00:00 AM

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Senior Specialist, AR
  • Damco Spain Sl
  • Little Rock, AR
  • A German Expert with F&A Background This role requires German proficiency (Speak/Write/Read) to perform Accounting Opera...
  • 4/24/2024 12:00:00 AM

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Production Engineer
  • Alten Technology Usa
  • Little Rock, AR
  • Were ALTEN Technology USA, an engineering company that provides solutions for engineering, technology, and product devel...
  • 4/23/2024 12:00:00 AM

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Credit Specialist (Waunakee-Hybrid)
  • Uniek Inc
  • Little Rock, AR
  • The Credit Specialist will perform a variety of accounting tasks for Accounts Receivable, General Accounting and Credit ...
  • 4/23/2024 12:00:00 AM

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Seasonal Sales Associate
  • Under Armour
  • Little Rock, AR
  • Values & Innovation At Under Armour, we are committed to empowering those who strive for more, and the company's values ...
  • 4/22/2024 12:00:00 AM

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Child Life Specialist I
  • Arkansas Children's
  • Little Rock, AR
  • ARKANSAS CHILDREN'S IS A TOBACCO FREE WORKPLACE. FLU VACCINES ARE REQUIRED. ARKANSAS CHILDREN'S IS AN EQUAL OPPORTUNITY ...
  • 4/22/2024 12:00:00 AM

Pine Bluff is the tenth-largest city in the state of Arkansas and the county seat of Jefferson County. It is the principal city of the Pine Bluff Metropolitan Statistical Area and part of the Little Rock-North Little Rock-Pine Bluff Combined Statistical Area. The population of the city was 49,083 in the 2010 Census with 2017 estimates showing a decline to 42,984. The city is situated in the Southeast section of the Arkansas Delta and straddles the Arkansas Timberlands region to its west. Its topography is flat with wide expanses of farmland, consistent with other places in the Delta Lowlands....
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Drug Safety/Medical Information Specialist jobs
$59,039 to $73,392
Pine Bluff, Arkansas area prices
were up 1.2% from a year ago