1,000+ matching jobs for “Audit Associate”

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Pfizer

Analista de Pesquisa Clínica Jr

São Paulo, São Paulo, Brazil

Full time
Regular

… • Drive Quality Event submission and remediation, when applicable • Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicable. QUALIFICATIONS: …

Added Oct 16, 2026

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State Street

Senior Claude Support Analyst - Assistant Manager

Bengaluru, India +1 location

Full time

… management repositories. Maintain Known Error Database (KEDB) and problem management records. Support audit reviews, compliance requirements, and operational evidence collection. Participate in hypercare activities …

Added Oct 27, 2026

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Amgen

C&Q Document Preparation Support (Facilities & Utilities)

India - Hyderabad

Full time
Regular

About the Role Amgen is seeking a Senior Associate specializing in Commissioning & Qualification (C&Q) to join the Engineering C&Q Center of Excellence (CoE). …

Added Oct 15, 2026

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The Home Depot

DC Quality Assurance Supervisor

ATLANTA RDC - 5250

In person
Full time
Regular

… DC management and associates. Monitors WMS releasese from the SSC and ensures succcessful roll-out. 10% Audit inbound shipments and directed by the SSC partners and create detailed reports of any deficiencies fround …

Added Nov 4, 2026

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Thermo Fisher Scientific

CRA / Sr CRA

Remote, Argentina +4 locations

Join Us as a Clinical Research Associate (CRA / Sr. CRA) At Thermo Fisher Scientific, our Clinical Research team supports leading pharmaceutical, …

Added Oct 16, 2026

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Thermo Fisher Scientific

Distribution Quality Technician - 1st Shift

Suwanee, Georgia, United States

… find cures for cancer. Location/Division Specific Information: The Supplier Relations Quality Control Associate is part of the Customer Channels Group (CCG) serving academic, pharmaceutical, biotech, government and …

Added Oct 16, 2026

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The Home Depot

Distribution Center- Quality Assurance Supervisor

BALTIMORE DFC - 5829

In person
Full time
Regular

Pay posted by employer$72,000–$82,000

Added Oct 16, 2026

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Amgen

R&D Supplier Quality Manager

United States - Remote

Full time
Regular

… across the supplier lifecycle. Key Responsibilities Conduct risk-based supplier assessments, qualification, audit and lifecycle management, including quality agreements across various R&D service categories. Lead or …

Added Oct 15, 2026

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Danaher

Senior Operations Coordinator

Istanbul, Istanbul, Turkey

Regular

… Maintain strong discipline around SOPs, quality requirements, EHS standards, inventory traceability and audit-ready documentation. Support ERP/WMS updates and ensure operational records are completed accurately and on …

Added Oct 15, 2026

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M&T Bank

Senior Administrative Assistant - Community Markets (Hybrid)

Buffalo, New York, United States +4 locations

Hybrid

Pay posted by employer$20.55–$34.25 per hour

… brand. Maintain M&T internal control standards, including timely implementation of internal and external audit points together with any issues raised by external regulators as applicable. Complete other related duties …

Added Nov 3, 2026

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M&T Bank

Software Engineer - Liquidity Reporting

Buffalo, New York, United States

Hybrid

Pay posted by employer$80,900–$134,800

… document root cause and remediation actions. Implement and maintain automated controls, reconciliations, audit evidence, operational procedures, and data lineage supporting Liquidity reporting and regulatory …

Added Nov 3, 2026

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Kenvue

RM & Compliance Senior Analyst

Asia Pacific, Philippines, Metro Manila, Taguig

Hybrid

… requirements is expected Talent Management: Demonstrates influencing skills and credibility. Assist Associate Compliance Manager and/or Compliance Manager in the implementation of compliance initiatives and related …

Added Oct 27, 2026

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Danaher

PMO Analyst

Bengaluru, Karnataka, India

Regular

… everything possible. The PMO Analyst supports project governance, reporting, forecasting, data quality, audit readiness, and continuous improvement across a global portfolio of Life Sciences software-as-a-service …

Added Oct 28, 2026

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Prudential Financial

Senior Infrastructure Security Engineer - Identity and Access Management (IAM)

Newark, New Jersey, United States

Pay posted by employer$104,000–$171,600

… testing, logging and change controls. · Collaborate with application owners, architects, risk, audit and global engineering teams to translate requirements into secure, supportable technical solutions. · …

Added Oct 27, 2026

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Bank of America

Business Control Manager - Global Payment Operations Business Controls

Charlotte, North Carolina, United States +2 locations

Pay posted by employer$95,900–$162,200

… effectiveness and provides subject matter expertise to support end-to-end issue management and Risk, Audit, and regulatory engagement and exam management. Responsibilities: Assesses the current-state testing …

Added Oct 27, 2026

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M&T Bank

Relationship Banker - Fells Point

Baltimore, Maryland, United States

In person

Pay posted by employer$22.61–$37.67 per hour

… planning, outreach, appointment preparation, interaction/appointment, follow-up) and Risk Management (audit requirements, fraud prevention, Know Your Customer (KYC) and customer information profile (CIP)). Complete …

Added Nov 3, 2026

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M&T Bank

Relationship Banker

Exeter, NH +1 location

In person

Pay posted by employer$23.84–$39.74

Added Nov 3, 2026

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M&T Bank

Relationship Banker

Watertown, Massachusetts, United States

In person

Pay posted by employer$23.84–$39.74 per hour

Added Nov 3, 2026

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M&T Bank

Relationship Banker - Old Saybrook, CT

Old Saybrook, CT

In person

Pay posted by employer$22.61–$37.67 per hour

Added Nov 3, 2026

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M&T Bank

Relationship Banker - Greece Branch

Greece, NY

In person

Pay posted by employer$20.55–$34.25 per hour

Added Nov 3, 2026

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Pfizer

Analista de Pesquisa Clínica Jr

São Paulo, São Paulo, Brazil

Full time
Regular

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QUALIFICATIONS · employer excerpt

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 1-year relevant experience in clinical research site monitoring and management
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience preferred

1 more in the full description below.

About this opportunity

Original employer description

The Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices, and Pfizer standards.

The Clinical Research Associate role is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders.

The Clinical Research Associate is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner, and other members of the study team, as required, in activities associated with the set-up, running and close out of sites in a clinical trial.

JOB RESPONSIBILITIES:

Responsible for investigator site management and monitoring for assigned sites: Clinical Trial Monitoring

• Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan and applicable prevailing laws, Good Clinical Practices, and Pfizer standards to achieve project goals, timelines and quality

• Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site initiation through to database lock, ensuring relevant timelines and quality deliverables are met.During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery

• Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites

• Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks

• Attend investigator meetings when required (virtual or F2F).

• Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level

• Conduct remote assessment of e diary data

• Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the Study Monitoring Plan, SOPs and commensurate with emerging issues and technologies.

• Monitor site level AEs and SAEs and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

• Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics

• Identify and resolve investigator site issues within required timeframes; agree and develop corrective and preventative actions with investigator and site personnel to close open issues and to prevent recurrence/persistence of issues

• Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines

• Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage conditions, and destruction activities.

• Support database release as needed

• May undertake the responsibilities of an unblinded monitor where appropriate.Clinical/Scientific and Site Monitoring Risk:

• Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team

• Interact with investigator site health care professionals in a manner which enhances Pfizer’s credibility, scientific leadership and in order to facilitate Pfizer’s clinical development goals

• Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators

• Drive Quality Event submission and remediation, when applicable

• Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development and checks, when applicable.

QUALIFICATIONS:

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 1-year relevant experience in clinical research site monitoring and management
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience preferred
Must be fluent in English and in the native language(s) of the country they will work in.

PHYSICAL/MENTAL REQUIREMENTS:

Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Demonstrated knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial
Ability to evaluate, interpret and present complex issues and data to support risk management and mitigation
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization.

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS:

Significant travel (60-80%) within area is required. May require some international travel and some weekend travel.

ORGANIZATIONAL RELATIONSHIPS:

Partners with Site Care Partner and Country SOM
Reports to Director of Clinical Site Operations, or Director of Site Management and Monitoring, or Site Care Partner III in some countries
When required Partners with other Study Team members e.g. Clinician, Recruitment Specialist, Clinical Data Scientist

Work Location Assignment: Remote

Last date to apply for job: Oct 21st

EEO (Equal Employment Opportunity) & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, or disability.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

Medical

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Keywords also found in description

Full time
Medical
Regular

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