Monitor technician Jobs in Newark, NJ

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Monitor technician • newark nj

Last updated: 6 days ago

Sr CRA Monitor - Ophthalmology

Planet PharmaNew York, NY, United States

Temporary

Target Pay Rate: 60-70/hr salary will be commensurate with experience.Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or re...Show more

Maintenance Technician

Griffin Global Systems IncNew York, NY, United States

Full-time

Required education and experience:.Experience working with automated beverage manufacturing equipment(examples: Crown Fillers, Angelus Seamers, Douglas Contour, Douglas Spectrum, RA Jones Meridian)...Show more

Maintenance Technician

Atria Senior LivingNew York, NY, United States

Full-time +1

We create communities where employees thrive in their work, helping our residents thrive in their homes.Atria Senior Living's family of brands has openings for individuals looking for a career with...Show more

Security Technician

Securitas TechnologyNew York, NY, United States

Full-time

Securitas Technology Corporation (STC) Technology and Solutions groups are experiencing tremendous success, and we currently have an Embedded Technician opening for team-oriented individuals posses...Show more

OB Technician

Wyckoff Heights Medical CenterNew York, NY, United States

Full-time

Assists patients with activities of daily living, provides basic nursing care to patients and assists.Registered Nurse in charge of the team and/or unit.Provides basic nursing care to patients that...Show more

Worksite Monitor

Children's AidNew York, NY, United States

Full-time

The Worksite Monitor conducts weekly assessments to ensure that youth work locations remain compliant with DYCD and DOL guidelines, thereby ensuring the safety and support of youth.The Worksite Mon...Show more

Gameday Monitor, MLB

H starNew York, NY, United States

Part-time

MLB is currently seeking part-time seasonal Gameday Monitors for the upcoming 2026 Major League Baseball season to provide quality assurance for live video and audio streams on MLB.Ideal candidates...Show more

MONITOR II

The GEO Group, Inc.Newark, NJ, United States

Full-time

Full-time employees will enjoy a competitive benefits package with options for you and your family including:.The compensation and benefits information is accurate as of the date of this posting.Th...Show more

Automotive Technician

Bridgestone AmericasMontclair, NJ, United States

Full-time +2

Bridgestone Retail Operations (BSRO) is part of Bridgestone Americas and employs over 22,000 teammates in North America.BSRO operates more than 2,200 company-owned stores, including Firestone Compl...Show more

Plumbing Technician

American DreamEast Rutherford, NJ, United States

Full-time

Triple Five Group, is an unparalleled mix of world-class entertainment, retail, and dining, comprising more than 3 million square feet just minutes away from New York City in East Rutherford, New J...Show more

HVAC Technician

RJY Group LLCNew York, NY, United States

Full-time

The HVAC Technician must be a Journeyman/woman skilled craftsman in their trade and have a minimum of five (5) years' actual, practical working experience in the industrial HVAC mechanical equipmen...Show more

Sterilization Technician

NYU Rory Meyers College of NursingNew York, NY, United States

Full-time

Sterilize dental instruments including instrument cassettes, bur blocks, endo file boxes, and handpieces.Track dental instruments through all phases of the cleaning and sterilization process by uti...Show more

Behavioral Technician

Flywheel CentersBayonne, NJ, United States

Full-time +1

Spend your day working with children with autism at home, in school, or center based.Carry out the treatment plan that has been carefully outlined by a supervising Board-Certified Behavior Analyst ...Show more

Monitor Technician

Jersey City Medical CenterJersey CIty, NJ, US

Full-time

Location: Jersey City Medical Center.Department Name: Telemetry Services.The above reflects the anticipated hourly wage range for this position if hired to work in New Jersey.The compensation offer...Show more

Security Monitor - Homeless Families

Urban Resource InstituteNew York, NY, United States

Permanent

Urban Resource Institute (URI).Across 24 shelters in New York City, URI provides safe housing for nearly 4,000 individuals and their pets every night and serves more than 40,000 people annually.URI...Show more

Lunch Monitor - Pierrepont Elementary School

Rutherford, NJ Public SchoolsRutherford, NJ, United States

Full-time

Lunch Monitor - Pierrepont School.Show more

Technician

RCM Health Care ServicesNew York, NY, United States

Full-time

Radiology Technician | Rad Tech.Valid licensure and / or certifications for state of work.Candidates must demonstrate ability to be flexible, adapt to fast paced environment, and remain professiona...Show more

Diesel Technician

Gabrielli Truck SalesNew York, NY, United States

Full-time

We are seeking a Ford Certified Diesel Service Technician to join our team.The role of the Diesel Mechanic is to perform repairs and maintenance on heavy-duty and medium-duty diesel vehicles in a f...Show more

Front Desk Monitor -PT

Volunteers of America - Greater New York (VOA-GNY)New York, NY, United States

Full-time +2

Volunteers of America-Greater New York (VOA-Greater New York) is an anti-poverty organization working to end homelessness in the New York area by 2050.We operate over 60 programs across New York Ci...Show more

Sr CRA Monitor - Ophthalmology

Planet PharmaNew York, NY, United States

13 days ago

Job type

Temporary

Job description

Job Description

Target Pay Rate: 60-70/hr salary will be commensurate with experience

Job Responsibilities:

Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes.
Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient as required/appropriate. Demonstrates diligence in protecting the confidentiality of each subject/patient. Assesses factors that might affect subject/patient's safety and clinical data integrity at an investigator/physician site such as protocol deviation/violations and pharmacovigilance issues.
Per the Clinical Monitoring/Site Management Plan (CMP/SMP):
Assesses site processes
Conducts Source Document Review of appropriate site source documents and medical records
Verifies required clinical data entered in the case report form (CRF) is accurate and complete via review of site source documents and medical records
Applies query resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query resolution to closure within agreed timelines
Utilizes available hardware and software to support the effective conduct of the clinical study data review and capture
Verifies site compliance with electronic data capture requirements.

May perform investigational product (IP) inventory, reconciliation and reviews storage and security. Verifies the IP has been dispensed and administered to subjects/patients according to the protocol. Verifies issues or risks associated with blinded or randomized information related to IP. Applies knowledge of GCP/local regulations and organizational procedures to ensure IP is appropriately (re)labelled, imported and released/returned.

Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations.

Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs and Clinical Monitoring Plan/Site Management Plan. Supports subject/patient recruitment, retention and awareness strategies. Enters data into tracking systems as required to track all observations, ongoing status and action items to resolution.

Understands project scope, budgets, and timelines for own and others' activities in the clinical team; manages site-level activities / communication to ensure project objectives, deliverables and timelines are met. Must be able to quickly adapt to changing priorities to achieve goals / targets.

May act as primary liaison with study site personnel, or in collaboration with Central Monitoring Associate. Ensures all assigned sites and project-specific site team members are trained and compliant with applicable requirements.

Prepares for and attends Investigator Meetings and/or sponsor face to face meetings. Participates in and may lead global clinical monitoring/project staff meetings (inclusive of Sponsor representation, as applicable) and attends clinical training sessions according to the project specific requirements. Provides guidance at the site and project level towards audit readiness standards and supports preparation for audit and required follow-up actions.

May provide direct supervision, training and/or mentorship to more junior level CRAs. Performs training and sign off visits for junior CRA staff, as assigned.

May be mentored and assigned lead tasks under supervision of an experienced Clinical Operations Lead (COL) or operational line manager. This could include participation in business development proposals and/or defense meetings.

Additional responsibilities include:

Site support throughout the study lifecycle from site identification through close-out

Knowledge of local requirements for real world late phase study designs

Chart abstraction activities and data collection

As required, collaborate and build relationship with Sponsor and other affiliates, medical science liaisons and local country staff

The SMA II may be requested to train junior staff

Identify and communicate out of scope activities to Lead CRA/Project Manager

Proactively suggest potential sites based on local knowledge of treatment patterns, patient advocacy and Health Care Provider (HCP) associations.

Identify operational efficiencies and process improvements

Develop study and country level informed consent forms

Collaborate with RWLP Regulatory team to ensure updated regulatory information is applied and shared

Participate in bid defense meetings

Provide input into Requests for Proposals (RFPs), scope and budgeting. Develop site management strategy.

Participate in Case Report Form design and edit check development.
What we're looking for:

Bachelor's degree or RN in a related field or equivalent combination of education, training and experience
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Must demonstrate good computer skills and be able to embrace new technologies
Excellent communication, presentation and interpersonal skills. Moderate level of critical thinking skills expected.
Ability to manage required travel of up to 75% on a regular basis

Equal Opportunity Employer: We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.

Fraud Alert: Candidate safety is a top priority at Planet Pharma. The industry has seen an increase in people falsely representing themselves as recruiters to gather personal information from job seekers. For your safety, do not provide sensitive data to anyone you have not spoken with thoroughly, never provide banking information during the application process and always double check the email address of the Recruiter to ensure it's from an official Planet Pharma domain (@planet-pharma.com, @planet-pharma.co.uk, and @ppgadvisorypartners.com) and not a domain with an alternative extension like .net, .org or .jobs.