1,000+ matching jobs for “Audit Associate”

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available

Chicago, Illinois, United States +5 locations

Pay posted by employer$66,800–$125,000

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

Added Oct 16, 2026

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Merck (MSD)

Associate Director, Functional Area Geography Lead, Costa Rica, Global Data Management & Standards, Clinical Data Management.

CRI - San Jose - San Jose (City Place)

As the Associate Director, Clinical Data Management (CDM) Geography Lead, you will play a key leadership role in shaping …

Added Oct 16, 2026

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Merck (MSD)

Associate Director, Governance Risk and Compliance for Data, Data Products and Digital Solutions

USA - Pennsylvania - North Wales (Upper Gwynedd) +1 location

Pay posted by employer$129,000–$203,100

… world. Join us in our mission to promote transparency, accountability, and ethical use of data and AI. The Associate Director, Governance Risk and Compliance for Data, Data Products and Digital Solutions will lead the …

Added Oct 18, 2026

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Thermo Fisher Scientific

Principal Clinical Research Associate (PCRA) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Remote, Germany +12 locations

… options available About the Role We are seeking a highly experienced Principal Clinical Research Associate (CRA) to lead and coordinate all aspects of clinical monitoring and site management for complex clinical …

Added Oct 16, 2026

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II / SR CRA I / SR CRA II) - US West - FSO

Remote, California, USA

Pay posted by employer$84,000–$120,000

Join Us as an Experienced 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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Thermo Fisher Scientific

Senior Clinical Research Associate (Sr CRA) / Senior Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Remote, Germany +11 locations

… and follow up on issues through resolution, applying root cause analysis and CAPA principles Maintain audit and inspection readiness at all assigned sites Build strong, collaborative relationships with investigators …

Added Oct 16, 2026

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II/Sr CRA) - AR, KS, LA, MO, OK, TX - Multiple Therapeutic Areas Available

Remote, Texas, USA

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

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Experienced Clinical Research Associate (CRA II/Sr. CRA I) - Oncology - Respiratory - Cardiovascular - US West

Remote, North Carolina, USA

… applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships with investigational sites. Detailed tasks and …

Added Oct 28, 2026

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Thermo Fisher Scientific

FSP Experienced Clinical Research Associate (CRA II/Sr. CRA I) - Oncology - Respiratory - Cardiovascular - US Southeast (Open)

Remote, North Carolina, USA

Added Oct 28, 2026

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Thermo Fisher Scientific

Clinical Research Associate II (CRA II) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Remote, Germany +12 locations

Added Oct 16, 2026

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Ferguson Enterprises

Senior Internal Auditor

Remote

Full time
Regular

… are proud of, at a company you can believe in. The Senior Internal Auditor reports to Manager – Internal Audit and plays an important role in assessing and enhancing business processes and internal controls across …

Added Oct 27, 2026

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TIAA

Sr IT Auditor

Dallas, Texas, United States

leads end-to-end audit engagements covering IT infrastructure, AI systems, data flows, cybersecurity controls, and operating …

Added Oct 27, 2026

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Capital One Financial

Principal Auditor, Global Payment Network

Nottingham, England, United Kingdom +1 location

This is a fantastic opportunity to join our UK Audit team. Capital One’s Audit function is a dedicated group of professionals focused on delivering top-quality …

Added Oct 27, 2026

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Capital One Financial

Senior Auditor, Global Payment Network

London, England, United Kingdom

This is a fantastic opportunity to join our UK Audit team. Capital One’s Audit function is a dedicated group of professionals focused on delivering top-quality …

Added Oct 31, 2026

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Biogen

Principal Auditor, Quality Audits

Baar, Zug, Switzerland

Hybrid
Full time
Regular

… expertise, engage with site leadership and senior quality stakeholders, and coach other auditors. At Senior Associate III level, you will independently lead audits and contribute to the execution of the regional audit …

Added Oct 15, 2026

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Cencora

Accounts Payable Supervisor

Vilnius, Vilnius, Lithuania

Full time

… data entry, debit balancing transfer & collections, discrepancy resolution, debit/credit and/or expense audit & processing functions within the Accounts Payable department. Responsibilites: Monitors the activities of …

Added Oct 27, 2026

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Ferguson Enterprises

Internal Auditor

Remote

… and conclusions. Present the results of work to management and persuade them of the benefits of the audit recommendations. Drive and lead the testing of the major business processes within the SOX Testing Program …

Added Nov 6, 2026

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Raymond James Financial

VP, Technology Risk Assurance

St. Petersburg, Florida, United States

Permanent

… and serves as a key partner to Technology, Cybersecurity, Risk Management, Compliance, Internal Audit, and business leadership. The role is responsible for ensuring transparent, effective, and proactive …

Added Nov 3, 2026

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Fiserv

Internal Auditor, Finance and Operations

Berkeley Heights, New Jersey +2 locations

Full time
Regular

Pay posted by employer$62,250–$99,600

Support execution of internal audit projects by conducting walkthroughs, testing controls, reviewing documentation, and summarizing results …

Added Nov 3, 2026

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Lowe's

Staff Auditor

Bengaluru, Karnataka, India

… to social impact and sustainability. For more information, visit Lowes India About the Team Internal Audit is an independent assurance/advisory function reporting functionally to the audit committee of the Board …

Added Oct 27, 2026

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available

Chicago, Illinois, United States +5 more

Pay posted by employer$66,800–$125,000

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Required Qualifications · employer excerpt

• 1–2 years of traveling on-site monitoring experience.
• Therapeutic experience in at least one of the following: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary.
• Candidates must live within 60 miles of the nearest major airport. Up to 80% travel is expected.

8 more in the full description below.

About this opportunity

Original employer description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (Level II) – 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 five 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 Clinical Research Associate (Level II), 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.

Required Qualifications

• 1–2 years of traveling on-site monitoring experience.

• Therapeutic experience in at least one of the following: Oncology, Ophthalmology, Neurology, Cardiology, Rare Disease, Respiratory, Obesity, and/or Pulmonary.

• Candidates must live within 60 miles of the nearest major airport. Up to 80% travel is expected.

• Must be legally authorized to work in the United States without sponsorship.

• Must be able to pass a comprehensive background check, including a drug screening.

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.
• 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. Performs 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.
• 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).
• 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 the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members.
• Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:
• Bachelor's degree in a life sciences related fieldor 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 1 years as a clinical research monitor) or completion of PPD Drug Development Fellowship.
• 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:
• Proven clinical monitoring skills
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
• Well-developed critical thinking skills, including but not limited to: critical mindset, in-depthinvestigation for appropriate root cause analysis and problem solving
• Ability to manage Risk Based Monitoring concepts and processes
• Good 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
• Good organizational and time management skills
• Effective interpersonal skills
• Attention to detail
• Ability to remain flexibile and adaptable in a wide range of scenarios
• Ability to work in a team or independently as required
• Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
• Good English language and grammar skills
• Good presentation skills

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

Compensation and Benefits

The salary range estimated for this position based in Illinois is $66,800.00–$125,000.00.

This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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