1,000+ matching jobs for “Audit Associate”

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Thermo Fisher Scientific

Sr Clinical Research Associate - FSP

Remote, Hungary

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 …

Added Oct 16, 2026

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Gilead Sciences

Associate Director, Data & AI Solutions

Tokyo, Japan

Full time
Regular

The Associate Director, Data & AI Solutions – Japan leads prioritized Data, Analytics, Automation, and Artificial …

Added Oct 15, 2026

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State Street

Alternative Ops Fund Accounting, Associate 2

Hangzhou, China 6 postings

Full time

… team members. · Support preparation of operational reports and client deliverables. · Maintain accurate audit trails and document management records. · Follow established procedures, risk controls and …

Added Oct 30, 2026

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BlackRock

Treasury – Liquidity Management, Associate

Dallas, Texas, United States

Full time
Regular

… resolve exceptions and control issues, maintain operating procedures and control documentation, and support audit and governance requests. Oversee workflow allocation, priorities and key performance indicators, serve as …

Added Oct 27, 2026

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Capital One Financial

MASE Compliance - Compliance Advisor Principal Associate

Richmond, Virginia, United States +4 locations

… subject matter expertise of applicable laws and regulations Engage and respond to inquiries from Internal Audit and Regulatory Examiners covering the scope of regulatory risk stemming from the use of scripts Conduct …

Added Nov 3, 2026

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Capital One Financial

Senior Tax Associate, Indirect Tax

McLean, Virginia, United States

Added Oct 27, 2026

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Merck (MSD)

Associate Specialist, Meeting Services Support

Petaling Jaya, Selangor, Malaysia

… enables operational excellence, financial stewardship, and consistent stakeholder experience worldwide. The Associate Specialist, Meeting Services Support supports the accurate and timely delivery of meeting administration …

Added Oct 16, 2026

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Gilead Sciences

Associate Director, Supply Chain

El Segundo, California, United States

Full time
Regular

Pay posted by employer$165,495–$214,170

… plans are in place where required. Act as the point of contact for managing internal audits, coordinating audit readiness activities, document requests, and response tracking across ES&P functions. Support/lead …

Added Oct 15, 2026

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Massachusetts Mutual Life Insurance

Investment Accounting Associate II - Derivatives

Boston, Massachusetts, United States +1 location

Full time
Regular

Pay posted by employer$99,800–$131,000

Investment Accounting Associate II - Derivatives Controllers Organization of Corporate Finance Full-Time/New York, NY and Boston, …

Added Nov 3, 2026

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Guardian Life Ins. Co. of America

Client Manager Associate, Northeast Select

Bethlehem, Pennsylvania, United States +1 location

Full time

Pay posted by employer$37,980–$62,392.50

… and support producers in meeting their business objectives? Guardian is seeking a Client Manager Associate, Select Market to support the retention and growth of our group insurance business. In this role, you will …

Added Oct 28, 2026

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Abbott Laboratories

Associate I Clinical Research

Alameda, California, United States

Pay posted by employer$73,900–$116,000

… staff in study planning, designing case report forms (CRFs), and training of study sites. Maintain and audit Trial Master File (TMF) and upload to eTMF to ensure inspection readiness. Perform review of clinical data …

Added Oct 28, 2026

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Prudential Financial

PGIM | Senior Associate, Fund Operations

Paris, Île-de-France, France

… our organization, so if this sounds exciting, then PGIM might be the place WHAT YOU CAN EXPECT As a Senior Associate within the Fund Operations team you will assume responsibility for the effective operation of …

Added Oct 27, 2026

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State Street

Alternative Ops Fund Accounting, Associate 1

Hangzhou, China 8 postings

Full time

Who we are looking for: Associate 1 Fund Accountant will be responsible for processing investment activity accounting entries, completing …

Added Oct 27, 2026

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U.S. Bancorp

Financial & Regulator Reporting Senior Associate

Milwaukee, Wisconsin, United States

Pay posted by employer$75,820–$89,200

… Reviews and coordinates fund expense analysis and expense processing. Prepares fund financial statements, audit and tax schedules. Location Expectations This role requires working from a U.S. Bank location three (3) or …

Added Nov 4, 2026

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Regeneron Pharmaceuticals

Associate Manager, Clinical Imaging Operations

TARRYTOWN +2 locations

Full time
Regular

Pay posted by employer$109,900–$179,300

… we use science and innovation to develop life-changing medicines for people with serious diseases. As an Associate Manager, Clinical Imaging Operations, you will have a central role in the execution of key operational …

Added Oct 16, 2026

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State Street

Alternative Ops Fund Accounting, Associate 2

Hangzhou, China 5 postings

Full time

… key fund operations, including investment activity processing, valuation, NAV package production, and audit-related activities. Join us if making your mark in the alternative investment industry from day one is a …

Added Oct 27, 2026

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State Street

Alternative Ops Fund Accounting, Associate 2

Hangzhou, China

Full time

Added Oct 27, 2026

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Capital One Financial

Sr. Associate, Capital Markets & Analytics

McLean, Virginia, United States

… 2+ years’ experience working with Capital Markets products Experience with risk management, compliance, audit, finance, or a combination Strong communication and presentation skills Strong critical thinking with an …

Added Oct 27, 2026

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Walt Disney

Manager or Associate Manager, Total Rewards

Minato-ku, Japan

Full time
Regular

… data accuracy and integrity. · Ensure appropriate documentation and controls are in place to support audit and compliance requirements. · Support offer approvals with the Talent Connection team and off-cycle …

Added Oct 27, 2026

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Medline

Associate HR Generalist (Redmond, OR)

Redmond, Oregon, United States

Pay posted by employer$58,000–$87,000

… ROLE MONDAY - FRIDAY THAT REQUIRES FLEXIBILITY FOR A MULTIPLE SHIFT OPERATION** Under supervision, the Associate HR Generalist provides guidance and solutions on human resources operational issues. In addition, this …

Added Nov 3, 2026

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Thermo Fisher Scientific

Sr Clinical Research Associate - FSP

Remote, Hungary

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About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Office

Job Description

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks.
Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities.
Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards.
Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution.
May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process.
Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
Valid driver's license where applicable
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manages Risk Based Monitoring concepts and processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Effective interpersonal skills
Strong attention to detail
Effective organizational and time management skills
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Excellent Hungarian language and grammar skills, good English language and grammar skills
Good presentation skills

Working Conditions and Environment:
• Working Conditions and Environment:
• Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
• Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.
• May also include extended overnight stays.
• Exposure to biological fluids with potential exposure to infectious organisms.
• Personal protective equipment required such as protective eyewear, garments and gloves.
• Exposure to fluctuating and/or extreme temperatures on rare occasions.
• Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.

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