Integrated Resources INC

Integrated Resources INC

Pharmacovigilance Scientist II

Montgomery, NJ, United States · Mid

Sponsorship not specifiedDetected 3332 days ago
Project ManagementExcelClinical TrialsClinical ResearchPharmacovigilanceSASResearchCommunicationMicrosoft Office

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odds of building a lasting career here

37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70

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Employer immigration record

from this employer's Department of Labor filings

Third-party placement is common here

23% of this employer's visa filings place the worker at a client company rather than at the employer itself, across 3 clients. Your visa, salary band and layoff exposure would follow the employer of record, not the client.Most common: Horizon BCBS · NYC Health & Hospitals Corporation · WEC Energy Group

Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.

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About the role

  • Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
  • IRI has built its reputation on excellent service and integrity since its inception in 1996.
  • We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Responsibilities

  • Scientist role is primarily responsible for the writing and review of safety supporting documents to support labelling changes/the development of new core safety information.
  • He/she will contribute or will be responsible for report writing and/or report ownership related to safety supporting documents.
  • Daily activities involve database searching, aggregate safety analysis and case level review, writing, planning, conducting meetings, and project management/coordination of strategic safety documents.
  • Scientist will partner with team members, stakeholders such as safety physicians, and a vendor.
  • Sr. Scientist would be responsible to contribute to or serve as report owner for supporting documents for safety-related labeling information.
  • Develop report strategy with stakeholders
  • Perform aggregate safety analysis and case level review
  • Perform literature searches and identify/analyze relevant publications
  • Author/contribute to the preparation of safety supporting documents
  • Partner with vendor to develop safety supporting documents/deliverables

Requirements

  • Scientist must be able to work on multiple projects simultaneously and prioritize tasks.
  • /Experience Required

Nice to have

  • Strongly Preferred

Benefits

  • Bachelor's degree in health or biomedical science (6+ years industry experience or equivalent) or
  • Advanced degree preferred in health or biomedical science (4+ year's industry experience or equivalent)
  • Clinical/medical writing and/or PV experience

Company info

  • Our mission centers on delivering only the best quality talent, the first time and every time.
  • We provide quality resources in four specialty areas:
  • Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
  • Pharmacovigilance Scientist II
  • Skillman, NJ, United States

This listing is sourced directly from Integrated Resources INC's careers page and normalized into a canonical job model.