1,000+ matching jobs for “Audit Associate”

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Apollo Global Management

Cyber MUM Associate

Mumbai (NESCO), India

Full time
Regular

… information on specific benefits. POSITION OVERVIEW: Apollo’s Cybersecurity team is currently seeking an Associate of Cyber Assurance, to join our dynamic and distributed Cyber Security team. The team is responsible for …

Added Oct 27, 2026

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Amgen

Associate Field effectiveness

India - Hyderabad

Full time
Regular

… transforming your career. What you will do Let's do this. Let's change the world. In this vital role, the Associate, Field Effectiveness will provide hands-on analytical and operational support that helps improve the …

Added Oct 16, 2026

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Amgen

Study Delivery Sr Associate

India - Hyderabad

Full time
Regular

Role Name: Study Delivery Senior Associate Role GCF: 4 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world’s toughest …

Added Oct 15, 2026

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IQVIA Holdings

Associate Manager, Specimen Management

Valencia, California, United States

Pay posted by employer$58,800–$122,500

The Associate Manager, Specimen Management supervises a team and oversees daily operations to ensure departmental …

Added Oct 15, 2026

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IQVIA Holdings

Associate Manager, Specimen Management

Valencia, California, United States

Pay posted by employer$58,800–$122,500

The Associate Manager, Specimen Management supervises a team and oversees daily operations to ensure departmental …

Added Oct 15, 2026

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Capital One Financial

Principal Associate, Accounting (Hybrid)

McLean, Virginia, United States +3 locations

… Degree or military experience At least 3 years of experience in accounting, external financial reporting, audit, finance, or a combination At least 3 years of experience with Google Workspace or Microsoft Office …

Added Oct 28, 2026

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Amgen

Associate Field Reporting

India - Hyderabad

Full time
Regular

… transforming your career. What you will do Let's do this. Let's change the world. In this vital role, the Associate, Field Reporting will provide hands-on technical and operational support for field and leadership …

Added Oct 15, 2026

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Capital One Financial

Insurance Risk - Senior Associate

McLean, Virginia, United States +1 location

… requirements to borrowers and agents, and evaluate vendor escalations to determine appropriate next steps. Audit Preparation: Compile, organize, and validate required documentation for internal and external audit …

Added Oct 27, 2026

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Campbell's

Associate Manager, Training

Lakeland, Florida, United States

Full time
Regular

Pay posted by employer$89,800–$123,500

How you will make history here... The Associate Manager, Training is responsible for leading, developing, and executing comprehensive training and …

Added Oct 27, 2026

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Pfizer

Senior Clinical Research Associate

Taipei, Taiwan, Taiwan

Full time
Regular

The Senior Clinical Research Associate is responsible for the site management, site monitoring and close-out of assigned clinical trials …

Added Oct 16, 2026

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Merck (MSD)

Clinical Research Associate

Taipei, Taiwan, Taiwan

… Expert (SME), buddy/mentor and sharing best practices as appropriate/required. • Supports and/or leads audit/inspection activities as needed. • Performs co-monitoring visits where appropriate. • Following the country …

Added Oct 16, 2026

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Pfizer

Associate - Quality Systems

Visakhapatnam, Andhra Pradesh, India

Full time
Regular

… Therefore, CICR, and electronic document management systems . Knowledge of official print management, audit trail review, metadata verification, document scanning, and record tracking . Understanding of Document …

Added Oct 16, 2026

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State Street

Middle Office - Senior Associate

Mumbai, India

Full time

Senior Associate – Transaction Management (Trade Settlements | Trade Confirmation | Static Data Maintenance) Job Title …

Added Oct 27, 2026

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Amgen

Sr Associate Field effetiveness

India - Hyderabad

Full time
Regular

Job Description - Sr Associate, Field Effectiveness Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of …

Added Oct 15, 2026

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TIAA

Associate - Quality Assurance - RKT

Pune, Maharashtra, India

… Required; 3+ Years Preferred Physical Requirements Physical Requirements: Sedentary Work Career Level 6IC Associate I QA RKT Related Skills Accountability, Automation, Business Acumen-Based Communication, Business Process …

Added Oct 27, 2026

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Merck (MSD)

Clinical Research Associate

Guaynabo, Guaynabo, Puerto Rico

Added Oct 16, 2026

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Thermo Fisher Scientific

Associate Manager Clinical Operations

Remote, Poland

… programs, minimize delays, and execute high-quality, cost-efficient clinical studies. Join Us as an Associate Manager Clinical Operations - Make an Impact at the Forefront of Innovation Summarized Purpose: The …

Added Oct 22, 2026

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Thermo Fisher Scientific

FSP Clinical Research Associate I/ Clinical Research Associate II

Remote, Israel

Join Us as a Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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State Street

Network Management, Senior Associate

Quincy, Massachusetts, United States +1 location

Full time

Pay posted by employer$52,000–$87,880

… and risk assessment process to ensuring monitoring an oversight obligation are met. Partner with Legal, Audit, Compliance, Risk, Operations, Product, and Relationship Management teams on Network Management -related …

Added Oct 27, 2026

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Accendra Health

Associate System Admin

3610 Accendra India

Full time

… Hands on experience using the iSeries command line using HMC. Manage offsite tape inventory (Iron Mountain) Audit offsite tape invoices and engage vendor as/if necessary. SUPPLEMENTAL JOB FUNCTIONS: Performs additional …

Added Oct 27, 2026

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Pfizer

Senior Clinical Research Associate

Taipei, Taiwan, Taiwan

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
Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience

1 more in the full description below.

About this opportunity

Original employer description

JOB SUMMARY

The Senior 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 Senior 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 Senior 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 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 required

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 heath 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 remediation, when applicable
Serve as a point of contact for audit conduct, and drive Audit Observation CAPA development andchecks, when applicable.

Other:

Mentor/train Clinical Research Associates as assigned
Serve as an SME for CRA-related processes
Participate in regional or local working groups/process improvement initiatives
Perform activities under guidance of a Site Care Partner prior to site activation e.g. feasibility and site selection, PTA, coordination of site activation checklist items, ICD finalization, SIV (as applicable), including management of issues that may compromise time to site activation
Conduct co-monitoring activities as requested

QUALIFICATIONS

Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
Extensive knowledge of clinical trial methodologies, ICH/GCP, FDA and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in both English and Mandarin.

PHYSICAL/MENTAL REQUIREMENTS

Advanced knowledge of clinical research and development processes and ability to gain command of process details

Demonstrated knowledge of global and local regulatory requirements
Advanced understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Advanced knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated ability to support sponsor regulatory interactions/inspections
Demonstrated knowledge of the processes around protocol design and feasibility assessment
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Proven 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
Proven 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
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required

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
Act as a mentor for Clinical Research Associates
Partner with other functional lines if engaged in a workstream/ LDT/ SME role

Work Location Assignment: Remote - Field Based

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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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Full time
Medical
Regular

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