Clinical Research Compliance & QA Analyst

Weill Cornell Medicine - Qatar

New York (NY)

On-site

USD 90,000 - 120,000

Full time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Job summary

Weill Cornell Medicine - Qatar seeks a Clinical Research Monitor to assist in implementing and operating quality assurance initiatives, including audits, DSMB activities, and education programs.

The role requires a Bachelor's degree and at least three years of related experience, with strong analytical, communication, and data management skills to ensure compliance with IRB and federal regulations.

Qualifications

  • Bachelor's degree required.
  • Minimum of three years related work experience.
  • Knowledge of IRB/DSMB operations and regulatory requirements.

Responsibilities

  • Participates in oversight of investigator/coordinator compliance with IRB requirements.
  • Plans, conducts, and reports internal quality audits to assure adherence to local and federal requirements.
  • Categorizes findings and tracks corrective actions to ensure data integrity.
  • Provides evaluations of compliance activities to the Assistant Director and stakeholders.
  • Assists with compliance training initiatives including coordinating sessions and developing materials.
  • Oversee data management activities, maintain databases, create reports for departments.
  • Prepare correspondence related to DSMB/IRB issues; review DSMB plans and regulatory documents.
  • Act as DSMB liaison to CTSC administrators and provide information as needed.
  • Serve as ESCRO administrator.

Skills

IRB compliance
DSMB operations
Audits
Data management
Analytical skills
Communication skills
Training coordination

Education

Bachelor's Degree in related field

Job description

Weill Cornell Medicine - Qatar seeks a Clinical Research Monitor to assist in implementing and operating quality assurance initiatives, including audits, DSMB activities, and education programs.

The role requires a Bachelor's degree and at least three years of related experience, with strong analytical, communication, and data management skills to ensure compliance with IRB and federal regulations.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Clinical Research Specialist - Trials & Compliance
Clinical Research Specialist - Trials & Compliance

Weill Cornell Medicine - Qatar • New York (NY)

On-site
USD 73,000 - 81,000
Clinical Research Nurse Specialist - Study Protocols & Care
Clinical Research Nurse Specialist - Study Protocols & Care

Weill Cornell Medicine - Qatar • New York (NY)

On-site
USD 90,000 - 130,000
Clinical Research Monitor - Hybrid, Quality & Compliance
Clinical Research Monitor - Hybrid, Quality & Compliance

OSF HealthCare • Peoria (IL)

Hybrid
USD 53,382 - 62,804
Clinical Quality & Patient Safety Leader
Clinical Quality & Patient Safety Leader

Weill Cornell Medicine - Qatar • New York (NY)

On-site
USD 123,900 - 146,500
Clinical Research QA & Monitoring Lead
Clinical Research QA & Monitoring Lead

ViziRecruiter,LLC. • New York (NY)

On-site
USD 85,000 - 115,000
Clinical Research QA Auditor
Clinical Research QA Auditor

University of Miami • United States

On-site
USD 70,000 - 100,000
Clinical Trials Quality & Compliance Lead
Clinical Trials Quality & Compliance Lead

Mount Sinai Health System • New York (NY)

On-site
USD 66,000 - 68,000
Field Clinical Research Associate - Site Monitoring
Field Clinical Research Associate - Site Monitoring

IQVIA • City of Rochester (NY)

On-site
USD 72,000 - 189,000
Clinical Research Monitor & Site Compliance Specialist
Clinical Research Monitor & Site Compliance Specialist

IQVIA Argentina • New City (NY)

On-site
USD 72,000 - 189,000
Clinical Quality & Compliance Monitor
Clinical Quality & Compliance Monitor

Mount Sinai Morningside • New York (NY)

On-site
USD 66,000 - 68,000