Central Monitor Job at Piper Companies (Silver Spring)

Assistant Nurse Manager, Central Monitoring Unit/Video Monitoring Unit

Responsible for overseeing, directing, and providing care to patients requiring ...

Location

United States , Jacksonville

Salary:

Not provided

Baptist Health (Florida)

Expiration Date

Until further notice

Requirements

Associate's Degree - Nursing
Medical Surgical Experience Required
Post- Surgical Nursing Experience Required
Nursing Experience
Basic Life Support (BLS) Required
Advanced Cardiac Life Support (ACLS) Required
Licensed Registered Nurse Required

Job Responsibility

Overseeing, directing, and providing care to patients requiring immediate treatment of any medical, surgical, or other condition, including chronic medical and minor injuries or illnesses

Fulltime

Unit Secretary - Monitoring Central Telemetry

Under the supervision of the Registered Nurse, the Unit Secretary performs the c...

Location

United States , Beaumont

Salary:

Not provided

CHRISTUS Health

Expiration Date

Until further notice

Requirements

High school diploma or equivalent preferred
certificate of completion from an approved course for Unit Secretary’s preferred
One (1) year Unit Secretary experience preferred, if there is no Unit Secretary certification
Six (6) months experience in a hospital preferred
Demonstrates required computer skills within one month of employment
Basic typing and prior computer skills preferred
For telemetry and/or critical care, successful completion of basic dysrhythmia course for unlicensed personnel within one month or after first available course offered
AHA BLS certification within two (2) weeks of employment

Job Responsibility

Transcribes physician’s orders from the chart to proper patient records accurately
Monitors intercom system
gives reassurance to patients
notifies nursing staff immediately of needs
Informs Charge Nurse of all pertinent information
Fosters positive physician relations
Displays telephone courtesy, answers promptly
Relays messages accurately to appropriate personnel
Informs patient/families of discharge procedure
Promptly removes patient from computer at time of discharge

Parttime

Unit Secretary - Monitoring Central Telemetry

Under the supervision of the Registered Nurse, the Unit Secretary performs the c...

Location

United States , Beaumont

Salary:

Not provided

CHRISTUS Health

Expiration Date

Until further notice

Requirements

High School diploma or equivalent preferred
Must possess good written and oral communication skills
Basic typing and prior computer skills preferred
One (1) year of experience preferred
EKG/arrhythmia interpretation background desired
Basic knowledge of medical terminology
Demonstrates required computer skills within one month of employment
AHA BLS certification within two (2) weeks of employment
Successful completion of basic arrhythmia course for unlicensed personnel within one month or after first available course offered

Job Responsibility

Transcribes physician’s orders from the chart to proper patient records accurately
Monitors intercom system
gives reassurance to patients
notifies nursing staff immediately of needs
Informs Charge Nurse of all pertinent information
Fosters positive physician relations
Displays telephone courtesy, answers promptly
Relays messages accurately to appropriate personnel
Informs patient/families of discharge procedure
Promptly removes patient from computer at time of discharge

Fulltime

Manager, Central Monitoring, Data Analysis - FSP

The Manager, Data Analysis, is responsible for overseeing centralized monitoring...

Location

United States

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

At least 4 years of relevant biotechnology/pharmaceutical industry experience
Minimum 2 years with direct RBQM systems experience
Technical expertise in database design, system configuration, and report development, with experience in managing Risk-Based Quality Management (RBQM) systems or similar platforms
Proficiency in programming languages such as Python, R, SQL, or SAS, with the ability to develop scripts for data analysis, automation, and system integration
Working knowledge of the clinical drug development process, including ICH, GCP guidelines, and regulatory requirements
Aptitude for mathematical concepts, statistical methodologies, and data analytics, with a focus on interpreting Key Risk Indicators (KRIs) and Key Performance Indicators (KPIs)
Knowledge and experience with clinical databases, electronic data capture systems, quality control processes, and auditing procedures
Proficiency in Microsoft Office applications, with advanced skills in Excel for data manipulation and reporting

Job Responsibility

Act as a subject matter expert for the configuration, implementation, and execution of Central Monitoring RBQM system across studies
Maintain Central Monitoring Key Risk Indicators and Quality Tolerance Limit Libraries within Central Monitoring RBQM system to ensure standard deployment consistency and alignment with regulatory requirements
Coordinate with functional and cross functional stakeholders to develop configuration specifications for Central Monitoring in RBQM system
Provide operational expertise, training, and guidance as a point of escalation for Central Monitoring issues related to Central Monitoring RBQM system
Conduct central monitoring reviews in support of study central monitor
Participate in ongoing improvements in standardizing technologies, systems, processes, and training materials that support Central Monitoring and RBQM
Represent Central Monitoring in process improvement initiatives
May require 25% travel

Specialist, Alarm Central

This position involves overseeing security alarm systems, monitoring alerts, and...

Location

United States , Bentonville

Salary:

21.00 - 40.00 USD / Hour

Walmart

Expiration Date

Until further notice

Requirements

Strong attention to detail
Experience with security or CCTV systems (preferred)
Ability to work independently
Clear and efficient communication skills
Customer service experience (preferred)
Basic computer skills
Alarm operations, alarm licensing, or related area (preferred)

Job Responsibility

Investigate alarms and alert appropriate authorities (security patrols, fire services, or police)
Assist associates with safety or security events
Monitor travel safety and security for assigned associates
Conduct reviews of multiple systems to detect potential risks
Coordinate corporate responses to safety/security events through advisories
Compile daily and incident reports
Follow company policies for managing incidents from minor issues to global crises
Ensure confidentiality of customer information

What we offer

Medical, vision and dental coverage
401(k)
Stock purchase
Company-paid life insurance
PTO (including sick leave)
Parental leave
Family care leave
Bereavement
Jury duty
Voting

Fulltime

Data Surveillance Analyst

The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and ...

Location

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Min. 2 to 3 years of relevant medical, clinical or data management work experience
Experience of working within an adaptive monitoring design study, and/or participating in a Central Monitoring/Data Surveillance process highly recommended
Basic SAS programming and/or SQL script writing required
Experience with CluePoints system required
Educated to a degree level (medical, biological science, pharmacy, and/or data analytics, preferred)
Fluent English – spoken & written
Familiarity with centralized monitoring and Data Driven Monitoring practices
Proficient in data analysis, trend identification, and issue triage
Knowledge of programing languages highly recommended
Risks management and control, quality management and assurance experience preferred

Job Responsibility

Support cross-functional study team with expertise of Data Surveillance Process and supporting technologies
Support the development of a robust Data Surveillance Plan, including Key Risk Indicators, Quality Tolerance Limits
Configure and Maintain Data Surveillance technologies (e.g., Clue Points Central Monitoring Platform)
Review relevant data via the scoped technologies, identifying findings related to trends, outliers, emerging risks, and systemic issues
Document findings from Data Surveillance review
Provide feedback and work with Technology teams to identify potential solutions that match the business and technology strategy
Perform presentations explaining identified findings to internal cross-functional study team and client team
Apply working knowledge and judgment to identify and evaluate potential data quality trend, outliers, and emergent issues
Determine and implement appropriate follow-up action with the input of other / relevant parties and / or guidance provided, if applicable
Actively participate in external or internal meetings and audits & regulatory inspections as required

What we offer

We offer competitive financial packages, training, and development
Expect exciting professional challenges but with a healthy work/life balance
We value your welfare just as highly as that of our patients
Parexel has a fully flexible work arrangement - you can be fully home based
But if you live close to our office and you want to use it, you are always welcome, and we will keep the desk ready for you

Data Surveillance Analyst

The Data Surveillance Analyst (DSA) is responsible for analyzing scientific and ...

Location

South Africa

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Min. 2 to 3 years of relevant medical, clinical or data management work experience
Experience of working within an adaptive monitoring design study, and/or participating in a Central Monitoring/Data Surveillance process highly recommended
Basic SAS programming and/or SQL script writing required
Experience with CluePoints system required
Educated to a degree level (medical, biological science, pharmacy, and/or data analytics, preferred)
Fluent English – spoken & written
Familiarity with centralized monitoring and Data Driven Monitoring practices
Proficient in data analysis, trend identification, and issue triage
Knowledge of programing languages highly recommended
Risks management and control, quality management and assurance experience preferred

Job Responsibility

Support cross-functional study team with expertise of Data Surveillance Process and supporting technologies
Support the development of a robust Data Surveillance Plan, including Key Risk Indicators, Quality Tolerance Limits
Configure and Maintain Data Surveillance technologies (e.g., Clue Points Central Monitoring Platform)
Review relevant data via the scoped technologies, identifying findings related to trends, outliers, emerging risks, and systemic issues
Document findings from Data Surveillance review
Provide feedback and work with Technology teams to identify potential solutions that match the business and technology strategy
Perform presentations explaining identified findings to internal cross-functional study team and client team
Apply working knowledge and judgment to identify and evaluate potential data quality trend, outliers, and emergent issues
Actively participate in external or internal meetings and audits & regulatory inspections as required
Recognize impact of study non-compliance/issues/delays/data quality signals and communicate/promptly escalate to FL any site and/or study issues that require immediate action

What we offer

Competitive financial packages, training, and development
Healthy work/life balance
Fully flexible work arrangement - you can be fully home based
Office desk available if you live close to our office

Data Scientist

The RBQM Data Scientist supports central monitoring and risk-based quality manag...

Location

United States , San Rafael

Salary:

76.00 - 100.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

PhD, MS, or BA/BS in statistics, biostatistics, computer science, data science, life science, or a related field
Relevant clinical development experience (programming, RBM/RBQM, Data Management), for example: PhD: 3+ years, MS: 5+ years, BA/BS: 8+ years
Advanced SAS programming skills (hard requirement) in a clinical trials environment (Base SAS, Macro, SAS SQL
experience with large, complex clinical datasets)
Hands-on experience working with clinical trial data
Proficiency with Microsoft Word, Excel, and PowerPoint
Knowledge of GCP, ICH, FDA guidance related to clinical trials and risk-based monitoring
Strong analytical and problem-solving skills
ability to interpret complex data and risk outputs
Effective communication and teamwork skills

Job Responsibility

Implement and maintain pre-defined KRIs, QTLs, and triggers using robust SAS programs/macros across multiple clinical studies
Extract, transform, and integrate data from EDC systems (e.g., RAVE) and other clinical sources into analysis-ready SAS datasets
Run routine and ad-hoc RBQM/central monitoring outputs (tables, listings, data extracts, dashboard feeds) to support signal detection and study review
Perform QC and troubleshooting of SAS code
ensure outputs are accurate and efficient
Maintain clear technical documentation (specifications, validation records, change logs) for all RBQM programs and processes
Collaborate with Central Monitors, Central Statistical Monitors, Data Management, Biostatistics, and Study Operations to understand requirements and ensure correct implementation of RBQM metrics

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Central Monitor

Piper Companies

Location:
United States , Silver Spring

Category:
IT - Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 20, 2026

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Job Responsibility:

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