Clinical Research Monitor Jobs

Medasource - New York, NY, United States

and a large network of participating clinical research sites to implement the study protocol and monitor study recruitment. Job Responsibilities: Support the development, preparation, and revision

from: linkedin.com - 2 days ago

American Clinical Research Services - Montclair, CA, United States

. We are seeking a Clinical Research Coordinator. LOCATION: On site in the Montclair, CA office SUMMARY The Clinical Research Coordinator will plan, direct, or coordinate clinical research projects

from: linkedin.com - 4 days ago

Velocity Clinical Research, Inc. - Hallandale Beach, Florida

protocol. Understand product development lifecycle and significance of protocol design includingcritical data points Understand the disease process or condition under study Collaborate with Clinical Research

from: resume-library.com - 3 days ago

Medix™ - ST Louis, MO, United States

as assigned. Requirements At least two years of experience as a clinical research coordinator. Excellent oral and written communication skills. Demonstrated ability to work well independently

from: linkedin.com - 4 days ago

Medix™ - ST Louis, MO, United States

professionals to execute research protocols effectively. Regulatory Compliance: Ensure adherence to all relevant regulatory requirements, including FDA guidelines, IRB approvals, and Good Clinical Practice (GCP

from: linkedin.com - 8 days ago

Pharmaceutical Research Associates, Inc - Emelle, Alabama

required to evaluate, initiate, monitor and close clinical sites in compliance with the Code of Federal Regulations and ICH/GCP Guidelines. We are currently looking for a Clinical Research Associate to join

from: resume-library.com - 3 days ago

Medix™ - ST Louis, MO, United States

to execute research protocols effectively. Regulatory Compliance: Ensure adherence to all relevant regulatory requirements, including FDA guidelines, IRB approvals, and Good Clinical Practice (GCP) standards

from: linkedin.com - 8 days ago

SQRL - Los Angeles, CA, United States

with sponsors, monitors, and regulatory authorities as needed. Training and Development: Provide training to research staff and ensure ongoing education on study protocols, procedures, and regulatory requirements

from: linkedin.com - 9 days ago

Renown Health - Reno, Nevada

, physician staff, study sponsors, and research participants. This position prepares, submits, and monitors documentation of research program activities while assuring compliance with regulations and protocols

from: HealtheCareers.com - 3 days ago

Ann & Robert H. Lurie Children's Hospital of Chicago - Chicago, IL, United States

at the direction of faculty to meet project objectives. 6. Reviews and coordinates time and effort reporting for faculty and clinical research staff. 7. Works with PIs to regularly monitor information and make

from: linkedin.com - 13 days ago