Jobs 1 - 20 out of 26 for Clinical Monitor

Top Companies Hiring for Clinical Monitor (Page 1 of 2)

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Luminate Medical
In-House Clinical Monitor
New York, NY, US
Onsite
Full-time
12 days ago
Conduct monitoring visits across clinical sites, perform source data review and verification, document findings, and ensure compliance with study protocols and regulatory requirements. Collaborate with internal teams to ensure high-quality clinical data and resolve monitoring findings.
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Actalent
Clinical Research Monitor
19133, Philadelphia, PA, US
Remote
Contract
$40–$50/hour
4 days ago
Support IND-regulated clinical trials by performing independent monitoring activities, ensuring compliance with FDA regulations and GCP guidelines. Manage Trial Master File documentation, conduct chart reviews, prepare monitoring reports, and collaborate with research and regulatory teams.
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LanceSoft
Clinical Research Monitor(CRA)
80239, Denver, CO, US
Remote
Full-time
8 days ago
Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements. Develop and maintain relationships with clinical investigators, CROs, affiliated hospitals, and research institutions. Review adverse event cases with in...
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Praxis Precision Medicines
Clinical Medical Monitor
United States
Remote
Full-time
$260k–$335k/year
13 days ago
Provide hands-on medical oversight for assigned clinical programs, support investigators and sites on eligibility, dosing, safety events, and other medical questions; review clinical and safety data; assess serious adverse events; and identify emerging signals or trends. Ensure medical monitoring, s...
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Dana-Farber Cancer Institute
Clinical Trials Senior Monitor
02446, Brookline, MA, US
Onsite
Full-time
$98.9k–$108.4k/year
11 days ago
The Clinical Trials Monitor ensures compliance with regulatory policies and guidelines, assists in the design and implementation of monitoring programs, and performs monitoring tasks for assigned clinical trials. Responsibilities include supervising monitoring personnel, coordinating monitoring cont...
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Dana-Farber Cancer Institute
Clinical Trials Senior Monitor
United States
Onsite
Full-time
$98.9k–$108.4k/year
11 days ago
The Clinical Trials Monitor ensures compliance with regulatory policies and guidelines, assists in the design and implementation of monitoring programs, and performs monitoring tasks for assigned clinical trials. Responsibilities include supervising monitoring personnel, coordinating monitoring cont...
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Dana--farber-Cancer-Institut
Clinical Trials Senior Monitor
02445, Brookline, MA, US
Hybrid
Full-time
$98.9k–$108.4k/year
12 days ago
The Clinical Trials Monitor ensures compliance with regulatory policies and guidelines, assists in the design and implementation of monitoring programs, and performs monitoring tasks through remote data review and onsite visits. Responsibilities include supervising monitoring personnel, coordinating...
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Caris Life Sciences
Clinical Data Monitor I
Texas, US
Onsite
Full-time
$74k–$84k/year
13 days ago
The Clinical Data Monitor is responsible for clinical data management activities for Caris sponsored and collaborating protocols and projects. This role ensures the highest standards of data integrity and quality in support of critical research efforts. Responsibilities include oversight and managem...
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State of Florida
Clinical Contract Monitor(Pharmacy)
United States
Onsite
Full-time
$53.9k–$113.7k/year
14 days ago
Oversee and ensure the quality, compliance, and clinical effectiveness of pharmacy services within a privatized healthcare system by providing expert monitoring, regulatory guidance, vendor training, and support. Manage compliance with key Florida statutes and administrative codes governing pharmace...
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Caris MPI, Inc.
Clinical Data Monitor I
Irving, TX, US
Onsite
Full-time
$74k–$84k/year
14 days ago
The Clinical Data Monitor is responsible for clinical data management activities, ensuring data integrity and quality for oncology research. Responsibilities include oversight of clinical investigative sites, quality control review of Case Report Forms, maintaining regulatory documentation, conducti...
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Oregon Health & Science University
Clinical Research Monitor (Research Project Manager)
Portland, OR, US
16 days ago
The Clinical Research Monitor contributes to the development and maintenance of Trial-Specific Monitoring Plans (TSMPs) and evaluates the conduct of clinical trials to ensure research integrity and compliance with protocols and regulations. Responsibilities include organizing monitoring activities, ...
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ImmunityBio
Senior Clinical Research Associate, Field Monitor
El Segundo, CA, US
Remote
Full-time
$128k–$140k/year
25 days ago
Senior Clinical Research Associate will participate in clinical research teams to ensure the most effective and efficient conduct of clinical research studies. This role plays a critical ownership part in driving the understanding and delivery of high-quality clinical research by providing expert pr...
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Guidehouse
Clinical Trials Program Monitor and Auditor
Bethesda, MD, US
Onsite
Full-time
$130k–$216k/year
26 days ago
Independently provide support services to satisfy the overall operational and clinical trial objectives of the National Institute of Allergy and Infectious Diseases (NIAID). Schedule and conduct site visits, develop and review clinical monitoring plans, review monitoring and audit reports, track rep...
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University of Chicago
Clinical Trials Monitor
Chicago, IL, US
$65k–$80k/year
about 1 month ago
Manages, facilitates, and monitors daily clinical research and clinical trial activities. Performs a variety of duties involved in the collection, documentation, analysis, and reporting of clinical research and clinical trial data. Ensures compliance of clinical research with federal, state, and loc...
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UTMB Health
Clinical Study Monitor, Research, Regulatory, & Compliance (Hybrid)
77555, Galveston, TX, US
Hybrid
about 1 month ago
Monitors the administrative components and progress of clinical research studies approved by UTMB Institutional Review Board (IRB). Ensures the safety of clinical trial participants and maintains the accuracy and integrity of trial data. Develops and maintains collaborative working relationships wit...
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Temple University Health System
Clinical Research Monitor II
Philadelphia, PA, US
over 2 months ago
The OCR Clinical Research Monitor II completes, revises, and reviews requirements for compliance with FDA and other regulatory bodies for clinical trial research. Monitors extramural research program investigator initiated studies and ensures protocol compliance at clinical research sites.
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Fred Hutchinson Cancer Center
Clinical Research Monitor II
98109, Seattle, WA, US
Onsite
Full-time
$97.8k–$146.7k/year
over 2 months ago
The Clinical Research Monitor II supports the quality and regulatory compliance of investigator-initiated oncology clinical trials. This role performs remote monitoring activities to ensure research is conducted in accordance with protocol requirements, Good Clinical Practice (GCP), and applicable r...
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Cornell University
Clinical Research Monitor
New York, NY, US
Onsite
Full-time
$43.68–$50.77/hour
over 2 months ago
Assist in the implementation and day-to-day operations of quality assurance and improvement initiatives, including audits and education programs. Oversee compliance with IRB and institutional requirements, conduct internal quality audits, track corrective actions, and maintain records related to DSM...
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Weill Cornell Medical College
Clinical Research Monitor
10176, New York, NY, US
Onsite
Full-time
$43.68–$50.77/hour
over 2 months ago
Assist in the implementation and day-to-day operations of quality assurance and improvement initiatives, including audits and compliance training. Oversee monitoring of investigator compliance with IRB and institutional requirements, conduct internal quality audits, and maintain records related to D...
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Mass General Brigham
Clinical Research Monitor
Boston, MA, US
$50.5k–$82.0k/year
over 2 months ago
Conduct site monitoring visits in accordance with standards of practice guidelines and federal regulations. Responsibilities include assessing protocol compliance, reviewing source documentation, drafting monitoring plans, providing training, maintaining communication with sites, documenting finding...
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Jobs 1 - 20 out of 26 for Clinical Monitor

Top Companies Hiring for Clinical Monitor (Page 1 of 2)

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