Clinchoice Inc.

Clinchoice Inc.

Clinical Project Manager II

Remote, US · Mid · Contract

Sponsorship not specifiedDetected 144 days ago
GCPComputer VisionProject ManagementExcelFEAClinical TrialsMedical DevicesResearchCommunicationMicrosoft Office

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odds of building a lasting career here

40Risky
Cap-exempt (no lottery)0
Sponsors this role90
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

Green-card filing pattern in this occupation

Context, not a finding about this posting: of this employer's 11 green-card filings in this occupation, 100% were for a worker who already held the job.

Green-card follow-through: 90%

Of 10 labor certifications old enough to have been used, 1 expired without the employer filing the next step. Median time from filing to decision: 490 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.

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

  • ClinChoice is a global full-service CRO committed to professional growth and a quality-driven "one-team" culture.
  • In this role, you will be responsible for the execution, oversight and delivery of clinical studies, including study tracking and management of vendor, site, and CRO activities.
  • Candidates should have prior CRO experience and a strong background managing complex oncology and hematology clinical trials.

Responsibilities

  • Performs, if necessary, co-monitoring visits for the assigned clinical projects.
  • Develop and implement alternative solutions to problems with study timelines, resources, budgets, etc.
  • Ensure issues are identified and communicated by the study team. Implement corrective action plan to prevent repetition of critical issues.
  • Manage any deviations on resources and hours spent on the project to be able to evaluate the project progress and profitability and identify change orders in a timely manner and implement corrective actions. Ensure budget discrepancies are documented.

Skills

  • University Degree in scientific, medical or paramedical disciplines.
  • Excellent knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements.
  • Experience managing complex clinical studies-oncology and hematology required.
  • Excellent English communication skills:written and verbal.
  • Ability to travel as required.
  • Excellent English communication
  • written and verbal.
  • The Application Process
  • About ClinChoice
  • Our Company Ethos
  • The success of these core values is evidenced by our below industry average turnover rates.
  • ClinChoice is an equal opportunity employer.

Benefits

  • Education, Experience and

Company info

  • We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.
  • Join our global team and help create a healthier world!

This listing is sourced directly from Clinchoice Inc.'s careers page and normalized into a canonical job model.