IQVIA

IQVIA

Associé(e) de recherche clinique (ARC) principal(e) or Attaché(e) de recherche clinique II / Senior Clinical Research

Kirkland, Quebec, Canada · Principal

Sponsorship not specified$84k-$137kDetected 3 days ago
GCPData ScienceExcelRecruitingHRISClinical TrialsClinical ResearchResearchCommunicationProblem SolvingMicrosoft OfficeGxP

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odds of building a lasting career here

53Sponsors, lottery-bound
Cap-exempt (no lottery)0
Sponsors this role100
Entry-level history0
PERM / green-card track0
Lottery odds (Level II)66
Fits your clock70

Sponsors, but it's cap-subject — you still face the weighted lottery (~30% per draw at Level II). Good if you win; have a cap-exempt backup on your list.

Lottery odds assume a STEM candidate.

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Employer immigration record

from this employer's Department of Labor filings

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 16 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 100%

Of 7 labor certifications old enough to have been used, 0 expired without the employer filing the next step. Median time from filing to decision: 493 days.100% of their filings were for a worker who already held the job.Only certifications past the 180-day window are counted — recent ones cannot have expired yet.

Reported a layoff in this occupation

In a green-card filing decided 2026-06-24, this employer stated it had laid off workers in Software Developers (NC) during the preceding six months. 3 such filings on record.Describes the period before that filing, not necessarily today. Unlike WARN notices this is occupation-specific and federal.

DOL often reclassifies their job titles

The Department of Labor assigned a different occupation than this employer requested on 54% of its 28 wage determinations — against a 18% norm. The occupation sets the prevailing wage floor.Reclassification is routine and can reflect genuinely hybrid roles; it is not by itself evidence of underpayment.

Files H-1B transfers

4 transfer filings in the last year, covering 4 workers. Median labor-condition decision: 316 days. An employer that already files transfers is one that can take over an existing H-1B.

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.

Community outcomes

No reports yet — be the first to help the next applicant.

About the role

  • Dans ce rôle, vous collaborerez avec les sites investigateurs et les équipes transversales afin de garantir que les études sont menées avec excellence, conformité et centrées sur les patients.
  • IQVIA est l'un des principaux fournisseurs mondiaux d'analyses avancées, de solutions technologiques et de services de recherche clinique pour le secteur des sciences de la vie.
  • IQVIA est un fournisseur mondial de premier plan de services de recherche clinique, d'informations commerciales et de renseignements sur les soins de santé pour les secteurs des sciences de la vie et de la santé.

Responsibilities

  • Work with sites to adapt, drive, and track subject recruitment plans according to project needs in order to improve predictability.
  • Deliver protocol and related study training to assigned sites and maintain regular communication with sites to manage expectations and resolve ongoing project issues.
  • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
  • Support study startup activities as needed.
  • Collaborate and coordinate with study team members to support project execution as needed.
  • Support development of site-specific patient recruitment plans when applicable.

Requirements

  • All information and credentials submitted in your application must be truthful and complete.
  • Create and maintain appropriate site management documentation, monitoring visit findings, and action plans by submitting monitoring reports, follow-up letters, and other required study documentation.

Compensation

  • $84k-$137k

Company info

  • Join a Team Advancing Clinical Research We are seeking a passionate and motivated Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials.

Visa & Work Authorization

  • conducted and study data are reported in accordance with the study protocol, applicable regulations and guidelines, and sponsor requirements
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This listing is sourced directly from IQVIA's careers page and normalized into a canonical job model.