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How much do centralized monitor clinical research jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for centralized monitor clinical research in the United States is $38.70, according to ZipRecruiter salary data. Most workers in this role earn between $38.22 and $39.18 per hour, depending on experience, location, and employer.

What is a centralized monitor in clinical research?

Centralized Monitors in clinical research are professionals who remotely oversee clinical trial data and site activities using advanced data analytics and centralized systems. They monitor data trends, identify discrepancies, and ensure protocol compliance without being physically present at the trial site. Their work helps improve data quality, enhance patient safety, and support on-site monitors by prioritizing sites or issues that need attention. Centralized monitoring is a key component of risk-based monitoring strategies in modern clinical trials.

What are the key skills and qualifications needed to thrive as a centralized monitor in clinical research?

To excel as a Centralized Monitor in Clinical Research, a solid background in life sciences, clinical trial processes, and regulatory guidelines like GCP is essential, often supported by a relevant degree. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and data analysis tools is typically required. Attention to detail, critical thinking, and effective communication are crucial soft skills for identifying risks and collaborating with study teams. These skills ensure data integrity, regulatory compliance, and efficient trial monitoring, which are vital for successful clinical research outcomes.

How does a centralized monitor collaborate with on-site clinical teams during a study?

Centralized Monitors work closely with on-site clinical teams by reviewing data remotely and providing timely feedback on potential discrepancies or compliance issues. They communicate findings through regular reports and virtual meetings, helping to proactively address problems and ensure data integrity. This collaboration is essential for maintaining study quality, and Centralized Monitors often serve as a liaison between the sponsor, site staff, and other monitoring roles. Effective communication and teamwork are key to the success of centralized monitoring in clinical research.

What is the difference between Centralized Monitor Clinical Research vs Site Monitor Clinical Research?

AspectCentralized Monitor Clinical ResearchSite Monitor Clinical Research
CredentialsTypically requires clinical research certifications, such as CCRP or CCRASimilar certifications, often with additional site-specific training
Work EnvironmentRemote, overseeing multiple sites from a central locationOn-site at clinical trial sites, visiting locations regularly
Employer & Industry UsagePharmaceutical companies, CROs, and biotech firmsResearch sites, hospitals, and clinical research organizations

Centralized Monitors oversee multiple clinical trial sites remotely, focusing on data quality and compliance, while Site Monitors conduct on-site visits to ensure proper trial conduct at individual locations. Both roles require similar certifications but differ mainly in work environment and daily responsibilities.

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Centralized Monitor Clinical Research jobs near you
Infographic showing various Centralized Monitor Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $80,500 per year, or $38.7 per hour.

Clinical Research Coordinator

Tandem Clinical Research

Marrero, LA • On-site

$20 - $26.75/hr

Full-time

Re-posted 12 days ago

Job description

Clinical Research Coordinator (CRC)
The Clinical Research Coordinator (CRC) is responsible for overseeing and managing the daily operational activities of assigned clinical research studies. This role works closely with investigators, clinical staff, study participants, sponsors, and CROs to ensure that all research activities are conducted in compliance with study protocols, regulatory requirements, and ethical standards.
The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.
Key Responsibilities
Study Management & Coordination
  • Organize, plan, and coordinate all aspects of assigned clinical trials from initiation through close-out.
  • Support study start-up activities including feasibility, regulatory submissions, and site activation.
  • Attend investigator meetings, site initiation visits, and other study-related meetings.
  • Manage visit schedules and coordinate study-related activities across clinical teams.

Recruitment, Enrollment & Consent
  • Collaborate with recruitment teams to support participant screening and enrollment.
  • Conduct informed consent discussions with participants, ensuring understanding of study requirements and documentation of consent.
  • Ensure protocol and regulatory requirements are met throughout the enrollment process.

Clinical Oversight & Subject Monitoring
  • Monitor and assess study subjects in accordance with protocol requirements.
  • Identify, document, and report adverse events in collaboration with the Principal Investigator and clinical staff.
  • Escalate safety concerns and protocol issues to the PI, sponsor, and IRB as required.

Documentation, Data & Systems
  • Maintain accurate and complete source documentation, case report forms, regulatory files, and study records.
  • Enter study data into EDC and other required systems and manage study databases.
  • Complete, verify, and resolve case report forms and sponsor or monitor queries in a timely manner.
  • Report protocol deviations to the PI, sponsor, and IRB as required.

Investigational Product & Specimen Management
  • Manage investigational product accountability records and documentation.
  • Collect, process, package, and ship study specimens per protocol requirements.
  • Perform phlebotomy and handle biological specimens in accordance with study protocols and safety guidelines, when trained and authorized.

Quality, Compliance & Team Support
  • Ensure all study activities comply with SOPs, GCP, and regulatory requirements.
  • Support quality assurance activities and audit readiness.
  • Provide assistance and mentorship to fellow coordinators as needed.
  • Maintain strict confidentiality of participant and study information.

Communication & Outreach
  • Serve as the primary point of contact for sponsor and CRO communications.
  • Participate in occasional outreach or community events related to clinical trials.
  • Ensure timely, accurate communication of study updates and issues.

Additional Responsibilities
This job description outlines the primary responsibilities of the Clinical Research Coordinator but is not exhaustive. Additional duties may be assigned as needed to support study requirements, operational needs, and organizational priorities. Responsibilities may evolve based on protocol complexity and business needs.
Requirements
  • Knowledge, Skills, and Abilities
  • Strong leadership and communication skills
  • Exceptional organizational and multitasking abilities
  • High attention to detail and commitment to regulatory compliance
  • Ability to work independently and collaboratively in a multidisciplinary environment
  • Strong time management and operational efficiency skills
  • Proficiency with office equipment and study-specific systems
  • Ability to maintain strict confidentiality
  • Required Experience & Qualifications
  • Education: Bachelor's degree in a related field
  • Experience: Minimum of two (2) years of clinical research or clinical trial management experience
  • Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN)
  • Phlebotomy: Prior experience performing blood draws and handling biological specimens required

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