Query Resolution jobs in United States

Senior Clinical Research Coordinator - Cardiovascular

DM Clinical Research · Posted Nov 12, 2026

Open

Tomball, Texas, United States
On-site
Full-time · Senior
4–5 years

Senior Clinical Research Coordinator - Cardiovascular

DM Clinical Research · Posted Nov 12, 2026

Open

Tomball, Texas, United States
On-site
Full-time · Senior
4–5 years

CRA II

ICON plc · Posted Nov 10, 2026

Open

Long Beach, California, United States
Full-time · Associate
$91K–$114K per year
2+ years

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Clinical Research Associate responsible for designing, analysing, and monitoring clinical trials.

Compensation

$91,336.00-$114,170.00

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolve queries to maintain high-quality clinical data
Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

Bachelor's degree in a scientific or healthcare-related field

Skills

clinical trial monitoring experience knowledge of ICH-GCP guidelines protocol compliance data integrity patient safety

CRA II

ICON plc · Posted Nov 10, 2026

Open

Long Beach, California, United States
$91K–$114K per year
2+ years

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Clinical Research Associate responsible for monitoring and managing clinical trials, ensuring protocol compliance, data integrity, and patient safety.

Compensation

$91,336.00-$114,170.00

Responsibilities

Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolution of queries to maintain high‑quality clinical data
Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

Bachelor's degree in a scientific or healthcare‑related field

Skills

clinical trial monitoring protocol compliance data integrity patient safety data review

CRA II

ICON plc · Posted Nov 10, 2026

Open

Sherman Oaks, California, United States
$91K–$114K per year
2+ years

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Clinical Research Associate II responsible for monitoring clinical trials, ensuring protocol compliance, and managing data integrity.

Compensation

$91,336.00-$114,170.00

Responsibilities

Conduct site qualification, initiation, monitoring, and close‑out visits for clinical trials
Ensure protocol compliance, data integrity, and patient safety throughout the trial process
Collaborate with investigators and site staff to facilitate smooth study conduct
Perform data review and resolution of queries to maintain high‑quality clinical data
Contribute to the preparation and review of study documentation, including protocols and clinical study reports

Requirements

Bachelor's degree in a scientific or healthcare‑related field

Skills

clinical trial monitoring protocol compliance data integrity patient safety data review query resolution

Clinical Research Coordinator II - Psychiatry

DM Clinical Research · Posted Nov 5, 2026

Open

Bellaire, Texas, United States
2+ years

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Coordinate and manage psychiatric clinical trials at assigned investigative sites, ensuring compliance with sponsor protocols, FDA regulations, and ICH/GCP guidelines.

Responsibilities

Complete required training including ICH-GCP and IATA certifications
Attend protocol and amendment trainings
Conduct study subject visits and document procedures
Enter data and resolve queries
Follow up on action items

Requirements

High School Diploma or equivalent
Bachelor's degree in Psychology, Neuroscience, Biology, Public Health, Nursing, or related health science discipline
Nice to have: Bilingual English/Spanish
Nice to have: ACRP certification

Skills

ICH-GCP certification IATA certification EDC usage IVRS usage data entry query resolution laboratory procedures

Data Compliance Coordinator

Thermo Fisher Scientific · Posted Nov 8, 2026

Open

Las Vegas, Nevada, United States
On-site
Associate

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Coordinate operational compliance activities across multiple clinical studies, ensuring data quality and regulatory compliance.

Responsibilities

Coordinate operational compliance activities across multiple studies
Maintain critical documentation
Work closely with monitors and sponsor representatives
Uphold data integrity standards
Optimize participant experiences in clinical trials

Requirements

Nice to have: Clinical research experience
Nice to have: Data management experience

Skills

ICH/GCP guidelines Electronic Case Report Form (eCRF) data entry Query resolution Investigator Site Files (ISF) maintenance Study documentation Microsoft Office applications Medical terminology

Clinical Research Coordinator II

Adams Clinical · Posted Nov 6, 2026

Open

Dallas, Texas, United States
$25–$30 per hour
1+ years

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Manage a portfolio of complex or high-volume clinical trials, oversee study operations, supervise staff, and ensure data quality and regulatory compliance.

Compensation

Pay: $25.00 - $30.00 per hour

Responsibilities

Independently manage a portfolio of complex and/or high-volume trials
Fully own study execution, including screening operations, enrollment progress, and SCF rates
Conduct all participant visits, clinical procedures, and eligibility assessments per protocol
Lead study start-up activities for assigned studies, including SIV preparation, regulatory readiness, and supply planning
Serve as the primary liaison with study sponsors, monitors, and CROs

Requirements

Bachelor’s degree required
Nice to have: experience with neuro and/or psych patient populations

Skills

clinical research coordination study operations protocol mastery data entry query resolution

Senior Clinical Research Coordinator - Cardiovascular

Senior Clinical Research Coordinator - Cardiovascular

Responsibilities

Requirements

Skills

CRA II

Compensation

Responsibilities

Requirements

Skills

CRA II

Compensation

Responsibilities

Requirements

Skills

CRA II

Compensation

Responsibilities

Requirements

Skills

Clinical Research Coordinator II - Psychiatry

Responsibilities

Requirements

Skills

Data Compliance Coordinator

Responsibilities

Requirements

Skills

Clinical Research Coordinator II

Compensation

Responsibilities

Requirements

Skills

Benefits

Benefits

Benefits

Benefits