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Central Monitor Jobs (NOW HIRING)

Monitor Technician 0112 Central Monitoring Schedule: Night Shift. 36 hours weekly. 6:00p-6:15a. Type additional details specific to position and/or department. About the Position The Monitor ...

Monitor Technician 0112 Central Monitoring Schedule: Night Shift. 36 hours weekly. 6:00p-6:15a. About the Position The Monitor Technician plays a crucial role in ensuring patient safety through ...

Monitor Technician 0112 Central Monitoring Schedule: Night Shift. 36 hours weekly. 6:00p-6:15a. About the Position The Monitor Technician plays a crucial role in ensuring patient safety through ...

Monitor Technician 0112 Central Monitoring Schedule: Night Shift. 36 hours weekly. 6:00p-6:15a. About the Position The Monitor Technician plays a crucial role in ensuring patient safety through ...

Monitor Technician 0112 Central Monitoring Schedule: PRN (As needed days & nights) Type additional details specific to position and/or department. About the Position The Monitor Technician plays a ...

Monitor Technician FT Nights 0112 Central Monitoring Schedule: Night Shift. 36 hours weekly. 6:00p-6:15a. Type additional details specific to position and/or department. About the Position The ...

Provides continual ECG surveillance at the Central Monitor Station. * Recognizes dysrhythmias and rhythm changes and reports them to the appropriate RN. * Accurately documents atrial and ventricular ...

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Central Monitor information

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How much do central monitor jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for central monitor in the United States is $16.90, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $17.55 per hour, depending on experience, location, and employer.

What is a central monitor?

Central Monitors are professionals who oversee clinical trials by remotely reviewing and analyzing trial data to ensure accuracy, consistency, and compliance with regulations. They help identify potential issues, trends, or risks in the data, allowing for proactive management of trial quality and patient safety. Central Monitors collaborate with site monitors, data managers, and study teams to address discrepancies and improve the overall conduct of the trial. Their work supports more efficient and targeted on-site monitoring, ultimately enhancing the reliability of clinical research.

How does a central monitor typically collaborate with site staff and other clinical research team members?

Central Monitors play a key role in clinical trials by remotely overseeing data quality and protocol compliance across multiple sites. They regularly communicate with site staff, data managers, and clinical research associates to address data discrepancies, clarify protocol requirements, and flag potential issues that require on-site follow-up. Collaboration is often facilitated through virtual meetings, email updates, and shared data platforms, ensuring that all parties are aligned on study progress and quality standards. This teamwork helps maintain trial integrity and supports the timely resolution of challenges that may arise during the study.

What are the key skills and qualifications needed to thrive as a central monitor, and why are they important?

To thrive as a Central Monitor, you need a strong background in clinical research, data management, and statistical analysis, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory compliance standards such as GCP is essential. Attention to detail, analytical thinking, and effective communication are crucial soft skills for identifying data inconsistencies and collaborating with cross-functional teams. These skills ensure the accuracy, integrity, and regulatory compliance of clinical trial data, which is vital for successful study outcomes.

What is the difference between Central Monitor vs Clinical Research Associate?

AspectCentral MonitorClinical Research Associate
CredentialsTypically requires a degree in life sciences or healthcare, with certifications like SOCRA or ACRPSimilar credentials, often with clinical trial certifications and relevant degrees
Work EnvironmentRemote or centralized office setting, overseeing multiple sitesOn-site at clinical trial sites or monitoring visits
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, academic institutions

Central Monitors primarily oversee clinical trial data remotely across multiple sites, focusing on data integrity and compliance. Clinical Research Associates (CRAs) often conduct on-site visits to monitor trial progress and site compliance. Both roles require similar qualifications but differ mainly in work setting and scope of responsibilities.

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Infographic showing various Central Monitor job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $35,147 per year, or $16.9 per hour.

Associate Director, Central Monitor - Hybrid

North Chicago, IL

AbbVie
Scientific Research and Development Services • 10K+ employees

Full-time

Re-posted 29 days ago


AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 103 frontline employees who took The Breakroom Quiz


Job description

Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

The Central Monitoring Associate Director is responsible for bringing science to life by leading a cross-functional team of Central Monitoring Managers charged with de-risking assigned clinical studies and thereby advancing AbbVie clinical research and development programs. The Central Monitoring Associate Director is accountable for service delivery results (quality, efficient, on-time and on-objective delivery) and for the building and strengthening the talent pipeline for today's needs and for the leaders of tomorrow.
The Associate Director of Central Monitoring role is a manager of manager position that will be filled when organizational size requires this level to manage span of control.

Responsibilities:

  • Responsible for maximizing the value and efficiently utilizing AbbVie's most valuable resource (staff) in the front-line Central Monitoring space. Leads, manages, and supervises a combined team of Central Monitoring Managers with delivery responsibilities for a portfolio of studies.
  • Creates an internal leadership talent pipeline and mentors/coaches team members on their leadership journey
  • Fosters a growth mindset within the team based on inclusive collaboration, innovation, learning and continuous improvement that delivers successful outcomes for the study, the team, the individual and the business.
  • Develops the central monitoring staffing strategy and tactics in support of assigned clinical research programs, to ensure execution is with quality and efficiency, on-time, and in line with company objectives.
  • Executes and manages the central monitoring staffing strategy including fluidly adjusting plans in support of project priorities and/or timelines plan.
  • Recruits, hires, and trains the front-line Central Monitoring Leadership team, including therapeutic area training, compliance training and study management-specific knowledge as required to perform assigned tasks.
  • Manages the performance cycle including expectation setting, objective setting (both tactical and stretch opportunities to ensure continuous growth), the provision of constructive and timely feedback (informal & formal, direct feedback as well as feedback from CDO business partners) reviews and management of any performance issues to resolution.
  • Interacts with and influences all levels of management and cross-functional team members in Clinical Development Operations to achieve high standards of output from front-line Central Monitoring Leadership staff.

**This is a hybrid based role working on-site T-TH. Candidates must be local to Marlow,  and work on-site 3 days a week. 

Qualifications
  • Education & Experience
    Bachelors degree in related field, may include life sciences, risk-based discipline.
    Extensive clinically related experience or data trend analysis experience, and people management experience (remote experience preferred).
    Experience working in an RBQM-model or similar experience with risk-based monitoring required.
    Experience/exposure to drug development, operations, risk management, successful decision-making, strategic execution
  • Make Possibilities Real
    Proven leadership skills in a cross-functional global team environment.
    Experience in managing remote/virtual teams and an ability to influence and align stakeholders, while modeling and driving AbbVie's leadership attributes.
    Ability to remove obstacles and provide support that enables direct reports to achieve results.
    Able to successfully coach and mentor both with direct reports and in a matrix environment.
  • Clear & Courageous
    Respectfully provides transparent, accurate and timely feedback to help direct reports improve performance.
  • Analytic & Critical Thinking Skills
    Strong analytical and critical thinking skills and the ability to evaluate complex issues from multiple perspectives and drive SMART SURE decision making and timely outcomes.
    Ability to anticipate and address critical issues; and develop contingency plans in a proactive manner.
  • Interpersonal & Communication Skills
    Acts with integrity in accordance with ABBVIE code of business conduct.
    Evangelist for RBQM within the organization, promoting value of early detection in de-risking studies.
    Strong English language skills-spoken, written, and conversational.
    Lead dynamic meetings and create engaging presentations.
  • Excellent interpersonal skills with the ability to communicate persuasively and with clarity, flexibility, and adaptability to changing requirements, resourcefulness, and creativity. Demonstrated proactive and positive team player.
    Able to maintain calm, cool, collected, and competent composure in high pressure situations in order to ensure successful hand-off to stakeholders responsible for taking action.
    Open and receptive to the gift of feedback in the pursuit of continuous improvement.
  • Organizational Skills
    Exhibits strong planning and organizational skills and high level of flexibility in a dynamic environment with competing projects and deadlines.
  • Computer Skills
    Comfortable with use/operation of data analytics and visualization tools for oversight.
    Competent with Microsoft Office applications (Outlook, Word, Excel, PowerPoint, and Teams).

GRADE AND BENEFITS WILL DEPEND ON LOCAL COUNTRY 

Additional Information

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html


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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013