Bus monitor serp_jobs.h1.location_city

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Bus monitor • pearland tx

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Clinical Trial QC Monitor

VirtualVocationsPasadena, Texas, United States

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A company is looking for a Clinical Trial QC Monitor.Key Responsibilities Performs comprehensive quality control monitoring of source documentation for clinical trials Generates QC reports summa...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days

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Bus Driver (CDL) & Handyman

The Goddard SchoolPearland, TX, US

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The Goddard School of Shadow Creek Ranch (Pearland), TX, is currently seeking a qualified CDL Bus Driver / Handyman to help maintain a safe, clean, and nurturing environment for our students and st...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30

Bus Driver #2572

Pearland ISDPearland, TX, US

serp_jobs.job_card.full_time

Provide safe, orderly, and efficient transportation of students to and from school and on extracurricular trips.Valid Class B Texas Commercial Driver’s License with passenger and school bus endorse...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days

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Bus Driver (CDL) & Handyman

The Goddard School of Pearland (Shadow Creek Ranch), TXPearland, TX, US

serp_jobs.job_card.full_time

BUS DRIVER / HANDYMAN (CDL REQUIRED).The Goddard School of Shadow Creek Ranch (Pearland), TX.Join our talented team, where we inspire children to be lifelong learners! Our.Safely transport children...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_hours

Clinical Trial QC Monitor

VirtualVocationsPasadena, Texas, United States

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A company is looking for a Clinical Trial QC Monitor.

Key Responsibilities

Performs comprehensive quality control monitoring of source documentation for clinical trials

Generates QC reports summarizing deviations, discrepancies, and missing documentation

Conducts QC monitoring, investigates protocol deviations, and provides training to relevant personnel

Required Qualifications

Bachelor's degree in a scientific field such as biology, chemistry, or nursing

Minimum of three years of experience as a Clinical Research Associate or clinical trial monitor, preferably in Oncology and / or Hematology

Strong understanding of IND procedures, study protocols, and regulatory requirements

Knowledge of Good Clinical Practice (GCP) guidelines and clinical research standards

Must obtain certification as a Clinical Research Associate (ACRP) or Clinical Research Professional (SoCRA) within one year of hire