IQVIA

IQVIA

Clinical Research Coordinator - Frisco, TX Role

Allen, TX · Junior · Part-time

No sponsorship$35k-$42kDetected 6 days ago
GCPClinical TrialsClinical ResearchMedical DevicesResearchGxP

Stay score

odds of building a lasting career here

42Risky
Cap-exempt (no lottery)0
Sponsors this role100
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70

Thin sponsorship signal and lottery-bound (~15% per draw). A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.

Lottery odds assume a STEM candidate.

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H-1B wage level

the lottery is wage-weighted — each level is one more entry

Level I · 1×
Level I$82,1601 entry
Level II$110,8432 entries
Level III$139,5063 entries
Level IV$168,1894 entries

The bottom of this range ($35,000) is below the Level I prevailing wage of $82,160. An H-1B cannot be filed below the prevailing wage, so an offer at the floor of this band could not be sponsored as posted.

DOL prevailing wage, 2026-27 wage year · Natural Sciences Managers (11-9121) · Dallas-Fort Worth-Arlington, TX. Wage level is derived by USCIS from the offered wage, occupation and worksite; the occupation shown is inferred from the job title.

Employer immigration record

from this employer's Department of Labor filings

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.

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

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About the role

  • This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
  • Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.
  • Collect and accurately record clinical data in case report forms (CRFs).

Responsibilities

  • Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.
  • Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.
  • Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
  • Collaborate with investigators and monitors, addressing queries and ensuring data quality.
  • Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Requirements

  • Minimum 1+ years of relevant work experience in clinical research.
  • Strong attention to detail and ability to establish effective working relationships.
  • Proficiency with EDC systems, data entry accuracy, and query management.
  • All information and credentials submitted in your application must be truthful and complete.
  • Bachelor's degree preferred or equivalent combination of education and relevant experience.
  • Working knowledge of clinical trials, GCP principles, and medical terminology.
  • Please note: This position is not eligible for sponsorship.
  • #LI-CES #LI-DNP #LI-HCP #ONSITE
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
  • IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
  • IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
  • The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience
  • location
  • and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Compensation

  • The potential base pay range for this role is $35.00-$42.00 per hour.

Benefits

  • IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward.
  • We partner with the world's leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation.
  • Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Company info

  • We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator.

Visa & Work Authorization

  • Please note: This position is not eligible for sponsorship.

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