
Remote Regulatory Associate (Latin and North Am)
Remote · USContract$25–30/hrSeen todaySeen in employer's feed today
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
The Regulatory Associate supports the Regulatory and Stewardship team by managing regulatory data and preparing compliant documents. The role coordinates with country regulatory managers, subject matter experts, manufacturing, and global teams, and includes developing and maintaining Safety Data Sheets for chemical products. It is fully remote and suited to recent graduates in scientific or information fields, or candidates with regulatory internship or relevant experience.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Remote Regulatory Associate (Latin and North America)
Location: Fully remote
Schedule: Monday–Friday, local standard business hours
Pay Rate: $25–30/hr
Assignment: 1-year contract with the ability to extend or convert
We are seeking a Regulatory Associate to support the Regulatory and Stewardship team with regulatory data management and the preparation of compliant documents for regulatory and business needs. This role involves working with country regulatory managers, subject matter experts, manufacturing, and global regulatory teams to coordinate document requests and maintain accurate records. This opportunity is suited to a recent graduate in information, chemistry, biology, or a related scientific field, or someone with a regulatory internship or relevant experience.
Responsibilities
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Coordinate the preparation and delivery of global regulatory documents in collaboration with Country Regulatory Managers (CRMs), subject matter experts, manufacturing, and global regulatory teams.
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Work with CRMs to understand local requirements and ensure document requests meet those requirements.
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Use tracking tools to maintain metrics, monitor requests, and support timely completion of documentation.
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Deliver completed documents to CRMs and archive copies for future reference and traceability.
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Communicate project status, timelines, and updates to key stakeholders.
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Consult with subject matter experts and global, regional, and country regulatory staff to clarify and implement document requirements.
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Independently manage shifting priorities based on incoming requests and document deadlines.
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Participate in team meetings and collaborate with global regulatory and business staff.
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Support continuous improvement initiatives and lead or participate in additional projects as needed.
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Develop and write Safety Data Sheets (SDSs) for chemical products, ensuring accuracy, completeness, and compliance with applicable regulations and standards.
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Stay informed about global and regional chemical safety regulations and SDS requirements.
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Gather and analyze information from scientific literature, test reports, and supplier documentation to support accurate SDS preparation.
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Maintain accurate records of SDSs and related documentation, ensuring accessibility for employees, customers, and regulatory authorities.
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Provide guidance and support to internal teams and external stakeholders on SDS-related questions.
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Update SDSs to reflect new information, regulatory changes, and product modifications.
Qualifications
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Minimum of a bachelor’s degree; a B.S. in information, chemistry, biology, or a related scientific field is preferred, or equivalent experience.
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Recent graduates and candidates with regulatory internship experience are encouraged to apply.
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Proficiency in Microsoft Excel, Word, PowerPoint, and SharePoint, along with familiarity with database environments.
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Strong project management and organizational skills.
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Excellent written and verbal communication skills.
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Ability to manage competing priorities and work within established timelines.
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Ability to work independently and collaboratively within a centralized team and across technical disciplines.
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Results-oriented approach to managing assignments and supporting team goals.
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Previous technical or regulatory experience preferred.
If you’re a recent graduate or early-career professional interested in regulatory work, this role offers the opportunity to support regulatory documentation, chemical safety information, and cross-functional projects in a fully remote environment. Apply today.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following benefits reflect Kelly's general offerings. Eligibility may vary by assignment, location, and job type. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here (https://www.mykelly.com/help-support-working-with-kelly-us/#Benefits) for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice (https://www.kellyservices.com/hubfs/myKelly/Resources/Employment\_Policies/Recruitment-Artificial-Intelligence-Notice.pdf?hsLang=en) .
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.
How this job compares
Set against the 1,026 open Regulatory Affairs jobs on Olive Jobs, counted November 13, 2026.
- Pay
- This posting$25–30/hr
- US median$26–40/hr48 hourly ranges
This range's midpoint, $27.50/hr, is 16% below the US median midpoint ($33/hr) — in the middle half of Regulatory Affairs hourly ranges across the US.
- Openings
- Olive Jobs lists 15 open Regulatory Affairs jobs in Indiana and 1,026 across the US. 17% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- Parexel56 open
- AbbVie44 open
- Otsuka America Pharmaceutical Inc.40 open
- Experience
- Regulatory Affairs postings that state a minimum ask for 7 years of experience at the median; the middle half ask for 5 to 10 years (910 postings).
- Education
- This posting asks for a bachelor's degree; 613 of the 1,026 open Regulatory Affairs jobs (60%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 13, 2026. Figures based on too few postings are left out.
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