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Clinical Monitoring Assistant Jobs (NOW HIRING)

Soliant Health

Clinical Infusion Pharmacist

Columbus, OH · On-site

$110K - $132K/yr

Monitor drug therapies, lab values, pharmacokinetic dosing, and TPN, making clinical ... Maintain compliance with pharmacy, healthcare, and regulatory standards. * Assist with pharmacy ...

Dana-Farber Cancer Institute

Under the direction of Clinical Trials Office Leadership, s/he will assist in the design, development, implementation, and conduct of an effective monitoring program in accordance with Good Clinical ...

Clingroup

Clinical Study Monitor-Animal Health

Fort Collins, CO · Remote

$33.25 - $45.25/hr

... * Assist in the preparation and review of study-related documentation, including monitoring ... Solid understanding of clinical monitoring processes, including site initiation, routine monitoring ...

Clingroup

Clinical Study Monitor-Animal Health

Fort Collins, CO · On-site

$33.25 - $45.25/hr

... * Assist in the preparation and review of study-related documentation, including monitoring ... Solid understanding of clinical monitoring processes, including site initiation, routine monitoring ...

Vanguard Clinical

Clinical Operations Associate (Pool)

CA · Remote

$70K - $80K/yr

... Clinical Monitoring, Quality Assurance, Data Management and Study Startup. As a small company, we ... Support collection, tracking, and review of essential documents. * Assist with feasibility ...

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

Manage the operational aspects of clinical trials (e.g., study management, site monitoring and ... * Assist in Development of and manage the study project plan, including timeline, budget, and ...

Precision Medicine Group, LLC.

Develop clinical monitoring strategies for assuring study timelines are met and assuring quality ... Accountable to assist sites, internal staff and CRAs with the preparation for GCP audits * Work ...

Prometrika, Llc

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

Manage the operational aspects of clinical trials (e.g., study management, site monitoring and ... * Assist in Development of and manage the study project plan, including timeline, budget, and ...

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Clinical Monitoring Assistant information

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How much do clinical monitoring assistant jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for clinical monitoring assistant in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What are the most commonly searched types of Clinical Monitoring jobs?

The most popular types of Clinical Monitoring jobs are:

What are popular job titles related to Clinical Monitoring Assistant jobs?

For Clinical Monitoring Assistant jobs, the most frequently searched job titles are:

Infographic showing various Clinical Monitoring Assistant job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Clinical Research Associate II, Phase I

Daytona Beach, FL • On-site

Jobtailor
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Posted 8 days ago

Job description

  • Provide a high standard of care for participants in clinical trials
  • Respond to emergency situations based upon clinical research standards
  • Conduct routine monitoring and close-out of clinical sites
  • Maintain study files
  • Conduct pre-study and initiation visits
  • Liaise with vendors
  • Manage study sites according to project plans
  • Ensure study staff receive proper materials and instructions to safely enroll patients
  • Verify informed consent procedures and protocol requirements comply with applicable regulations
  • Ensure integrity of data submitted on CRFs and other data collection tools
  • Monitor data for missing or implausible data
  • Manage study registries according to project plans
  • Undertake feasibility work when requested
  • Complete SAE reporting, reports, narratives, and follow-up of SAEs
  • Perform CRF review and query generation and resolution in Fortrea or client data management systems
  • Assist with training new employees through co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator, with supervision if applicable
  • Act as a local client contact as assigned
  • Perform other duties assigned by management
Requirements
  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 1+ years of Clinical Monitoring experience
  • Phase I experience
  • 40-50% overnight travel
  • Ability to work in a fast-paced environment with strict study-protocol timelines
  • Ability to adapt to changing priorities
  • Teamwork and people skills
  • Comfort working in a technology-based electronic data environment
  • Ability to sit for extended periods and operate a vehicle safely
  • Repetitive hand movement of both hands, with ability to make fast, simple, repeated movements of fingers, hands, and wrists
  • Ability to crouch, stoop, bend, and twist upper body and neck
  • Ability to access and use a variety of computer software
  • Ability to lift and carry 15-20 lbs.
  • Regular and consistent attendance
  • Varied hours may be required
Core Competencies

Demonstrates expertise in Clinical Monitoring and Project Coordination, ensuring compliance with clinical research standards and effective management of study sites. Proficient in data integrity verification and participant care within clinical trials.

Highest-signal resume keywords
  • Clinical Monitoring Experience
  • Phase I Experience
  • Nursing Licensure
  • Data Management Systems
  • Emergency Response
Hard Skills
  • Clinical Trial Management
  • Data Collection Tools
  • CRF Review
  • SAE Reporting
  • Feasibility Assessment
  • Study Protocol Compliance
  • Monitoring Data Integrity
  • Study Site Management
  • Patient Enrollment Procedures
  • Vendor Liaison
Soft Skills
  • Teamwork
  • Adaptability
  • Communication Skills
  • People Skills
  • Time Management
Certifications & Qualifications
  • University Degree
  • Certification in Allied Health Profession
Industry Keywords
  • Clinical Trials
  • Clinical Research Standards
  • Informed Consent Procedures
  • Study Files Maintenance
  • Project Plans
Tools & Technologies
  • Electronic Data Environment
  • Fortrea
  • Data Management Systems
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