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Notary Field Inspector Jobs in Ohio (NOW HIRING)

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Notary Field Inspector information

What is a notary field inspector?

Notary Field Inspectors are professionals who visit various properties or locations to verify details, take photographs, and complete inspection reports, often on behalf of lenders, insurance companies, or government agencies. They also carry a notary commission, which allows them to notarize documents on-site as needed. Their work ensures that property or asset information is accurate and that required documents are legally validated. This role often requires travel, attention to detail, and strong organizational skills. Notary Field Inspectors play an important part in property transactions, loan processing, and insurance claims.

What are the key skills and qualifications needed to thrive as a notary field inspector?

To thrive as a Notary Field Inspector, you need a notary commission, strong attention to detail, and a solid understanding of property inspection procedures. Familiarity with digital inspection tools, mobile apps for reporting, and secure document handling systems is typically required. Excellent organizational skills, professionalism, and effective communication help build trust with clients and ensure accurate reporting. These skills are vital for maintaining legal compliance, providing reliable inspection results, and upholding the integrity of notarized documents.

What are some common challenges faced by notary field inspectors during property inspections?

Notary Field Inspectors often face challenges such as coordinating schedules with property owners, working in varying weather conditions, and ensuring all documentation is completed accurately and promptly. Additionally, inspectors must be prepared to handle unexpected situations on-site, such as inaccessible properties or uncooperative occupants. Developing strong communication skills and maintaining meticulous records are essential for overcoming these challenges and ensuring each inspection meets industry and legal standards.

How much do notary field inspectors make?

Notary field inspectors typically earn between $15 and $25 per hour, with annual salaries ranging from approximately $30,000 to $50,000 depending on experience, location, and workload. Many inspectors work on a contract basis, and income can vary based on the number of inspections completed and certifications held.

How to become a notary field inspector in PA?

To become a notary field inspector, you must be at least 18 years old, a resident of Pennsylvania, and pass a background check. You need to complete a state-approved notary education course and submit an application to the Pennsylvania Department of State, along with the required fee. Once commissioned, you may need to obtain specific inspection training and tools to perform field assessments effectively.

Which notary field inspector job makes the most money?

Notary field inspectors with specialized skills, such as those handling complex or high-value transactions, tend to earn higher wages. Experience, certifications, and working in high-demand regions can also increase earning potential. Generally, those working for larger companies or in metropolitan areas tend to make more money.
Infographic showing various Notary Field Inspector job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 90% Full Time, 7% Part Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.

Strategist, Regulatory Affairs

ClinChoice

Cincinnati, OH

Full-time

Posted 12 days ago


Job description

ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative "one-team" culture. We are looking for a dynamic person to join our in-house team as a Associate, Regulatory Affairs (ONSITE) on a permanent basis at Cincinnati, OH.

Join our team: you can be part of making a difference in peoples' lives and experience a fulfilling and rewarding career!

Job Title: Strategist, Regulatory Affairs

Employment Type: Full Time

Location: Hybrid (Cincinnati, Ohio) - Location Address: 4545 Creek Rd Blue Ash, OH 45242

  • Responsible for managing, planning, preparation, and delivery of documents both electronic- and paper-based in support of assigned. global regulatory product registrations, renewals, tenders/customs, etc.
  • Coordinate the preparation and submission of medical device applications by providing regulatory information and documents and following up closely on queries from inspection through approval.
  • Prepare and/or review letters of authorization, cover letters for registration certificates, declarations, power of attorney, and other regulatory documentation to ensure accuracy, appropriateness, and consistency of documents intended for various global regulatory submissions.
  • Submit and manage applications for the US FDA Certificates to Foreign Government (CFGs).
  • Maintain various tracking tools to ensure up-to-date information and traceability of all regulatory data/documentation.
  • Perform and/or coordinate legalization, notarization, and apostille of regulatory documents
  • Ensure compliance with current good documentation practices, including but not limited to proofreading, formatting, indexing and recordkeeping.
  • Assist all regions in answering inquiries and providing required documents and information utilizing various search tools and systems.
  • Perform document filing and retrieval functions as directed and per company's policies and procedures.
  • Effectively communicate with internal and external teams and/or clients as to the status of deliverables, to ensure timely and satisfactory completion of tasks and expectations.
  • Communicate with the project teams on a regular basis regarding regulatory updates.
  • Provide support to internal and external teams to address various technical inquiries and provide requested data/information
  • Participate in group meetings and provide tactical approaches to addressing issues of basic complexity
  • Perform other tasks as assigned.

 

Experience/Skills

 

  • Bachelor's degree (Life Sciences or a regulatory related field preferred)
  • Minimum of 1 year of hands-on experience in medical device regulatory affairs, or at least 3 years of combined regulatory affairs and related experience.
  • Basic knowledge of US FDA QSR, ISO 13485, EU MDD/MDR.
  • Knowledge of global medical devices registration process is a plus
  • Proficient in Microsoft Office (e.g., Word, Excel, PowerPoint)
  • Have a good understanding of current Good Documentation Practices in a regulatory environment.
  • Self-starter with the ability to work in a team environment and on projects of diverse scope where analysis of a situation or data requires evaluation of various factors with minimal supervision.
  • Excellent organizational skills with strong attention to detail, effective planning, and the ability to multitask efficiently
  • Must possess excellent written and verbal communication skills.

The Application Process

Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.

Who will you be working for?

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.           

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below industry average turnover rates.

ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.


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