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Regulatory Agencies Jobs (NOW HIRING)

Jobtailor

Manager, Regulatory Affairs

Lake Forest, IL · On-site

$110 - $160/hr

Author with team members, regulatory submissions for the Infusion Systems infusion pump product portfolio. • Acts as a point person for regulatory agency interactions (either written or oral ...

New

Dudley Land Company

Regulatory Analyst

Houston, TX

This role serves as the primary liaison between the company and federal, state, and local regulatory agencies and ensures full compliance with applicable laws, regulations, and permit conditions ...

CSAA

Regulatory Reporting Analyst- Remote

Oregon, IL · Remote

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Regulatory Reporting Analyst- Remote

Nevada, IA · Remote

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Regulatory Reporting Analyst- Remote

Iowa, LA · Remote

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

CSAA

Serve as the primary point of contact with regulatory agencies, proactively communicating regarding data clarifications, reporting requirements, and submission timelines, including extension requests ...

New

Mewbourne Oil Company

Regulatory Analyst

Midland, TX · On-site

Interact professionally with regulatory agencies and respond to requests promptly. * Manage all regulatory and permitting activities associated with well operations. * Prepare and file reports ...

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Regulatory Agencies information

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How much do regulatory agencies jobs pay per year?

As of Aug 8, 2026, the average yearly pay for regulatory agencies in the United States is $95,411.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $112,000.00 per year, depending on experience, location, and employer.

What is the main job of regulatory agencies?

Regulatory agencies are responsible for creating and enforcing rules and standards to ensure safety, fairness, and compliance within specific industries or sectors. They monitor organizations, conduct inspections, and issue permits or sanctions as needed to protect public interests. Their work often involves reviewing applications, conducting investigations, and collaborating with stakeholders to maintain regulatory compliance.

What are some typical challenges faced when working at a regulatory agency, and how can new employees prepare for them?

Working at a regulatory agency often involves navigating complex regulations, balancing public interests with industry concerns, and keeping up with frequent changes in laws and policies. New employees may find it challenging to quickly understand technical jargon and the legal framework governing their area. To prepare, it's beneficial to review recent regulatory updates, familiarize yourself with the agency's mission, and develop strong communication skills for collaborating with both internal teams and external stakeholders.

What are the key skills and qualifications needed to thrive in a regulatory agency role, and why are they important?

To thrive in a regulatory agency role, you typically need a background in law, public policy, or a relevant technical field, along with strong analytical and compliance skills. Familiarity with regulatory databases, compliance management software, and sometimes industry-specific certifications is important. Excellent communication, ethical judgment, and attention to detail help professionals collaborate with stakeholders and enforce regulations effectively. These skills ensure that regulatory standards are upheld, protecting public interests and maintaining industry integrity.

What is the difference between Regulatory Agencies vs Compliance Officers?

AspectRegulatory AgenciesCompliance Officers
CredentialsVaries by agency, often includes degrees in law, public policy, or related fieldsCertifications like Certified Compliance & Ethics Professional (CCEP), degrees in law, business, or related fields
Work EnvironmentGovernment offices, regulatory bodies, often in policy or oversight rolesCorporate settings, financial institutions, healthcare, ensuring company adherence to laws
Employer & Industry UsageGovernment agencies overseeing industries like finance, healthcare, environmentPrivate companies, organizations across various sectors requiring legal and regulatory adherence
Common Search & ComparisonUnderstanding roles in regulation and oversightEnsuring company compliance with laws and regulations

Regulatory Agencies are government bodies responsible for creating and enforcing rules within specific industries, while Compliance Officers work within organizations to ensure adherence to these regulations. Both roles require similar credentials and often collaborate to maintain legal and ethical standards in their respective environments.

What is a regulatory agency?

Regulatory agencies are government bodies responsible for creating, implementing, and enforcing rules and regulations within specific sectors, such as finance, healthcare, or the environment. Their primary goal is to protect public interest by ensuring compliance with laws and standards. These agencies can issue licenses, monitor industry practices, conduct inspections, and take action against violations. Examples include the Environmental Protection Agency (EPA) and the Food and Drug Administration (FDA) in the United States.
More about Regulatory Agencies jobs
What job categories do people searching Regulatory Agencies jobs look for? The top searched job categories for Regulatory Agencies jobs are:
Regulatory Agencies jobs near you
Infographic showing various Regulatory Agencies job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 9% Part Time, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $95,411 per year, or $45.9 per hour.

Regulatory Affairs Associate - Clinical Research

Baylor College of Medicine

Houston, TX • On-site

$70K - $83K/yr

Full-time

Re-posted 9 days ago

Baylor College of Medicine rating

8.0

Company rating: 8.0 out of 10

Based on 24 frontline employees who took The Breakroom Quiz

184th of 616 rated colleges and universities

Job description

Regulatory Affairs Associate - Clinical Research
Division: Pediatrics
Work Arrangement: Onsite only
Location: Houston, TX
Salary Range: $70,618 - $83,080
FLSA Status: Exempt
Work Schedule: Monday - Friday, 8 a.m. - 5 p.m.
Summary
The Regulatory Affairs Associate works to support the Protocol Office and investigators associated with Baylor College of Medicine Department of Pediatrics at The Texas Children's Cancer and Hematology Centers (TXCH). This position supports all aspects of regulatory compliance for a specified portfolio of clinical trials. This support includes, but is not limited to, reviewing protocols and protocol related documents, submitting protocols to regulatory agencies and review committees and ensuring successful navigation of approval processes for clinical research. This position requires expertise and understanding of clinical research and applicable regulations.
Employees with Certified Clinical Research Professional (CCRP) or Certified Clinical Research Coordinator (CCRC) certification are eligible for certification pay.
Job Duties
  • Coordinates regulatory correspondence across internal stakeholders and external institutions.
  • Prepares protocol documents and required regulatory forms in order to obtain institutional and regulatory agency approval for the conduct of clinical research projects at the TXCH.
  • Maintains and expands understanding of federal regulations, ICH GCP guidelines and internal SOPs by producing work in compliance with those regulations, guidelines and SOPs.
  • Maintains working knowledge of regulatory requirements through independent continuing education using guidelines, articles, and courses.
  • Develops and maintains positive relationships with institutional review committees and sponsor through oral and written communications.
  • Acts as a liaison between institutional review committees, regulatory agencies and the investigators to ensure that protocols obtain applicable approvals, that protocol amendments are submitted appropriately and that annual renewals are obtained.
  • Facilitates investigators in reporting and responding to institutional review committees' and other regulatory agencies' inquiries or comments.
  • Provides input to the investigators in consent form creation and protocol editing.
  • Works closely with the study team, research staff, and investigators to assure that all regulatory documents for the research studies are up-to-date.
  • Prepares for FDA meetings, inspections, and audits from regulatory authorities. Is available on site during audit visit to reply to auditor inquiries.
  • Facilitates communication with IRB and other applicable agencies related to Adverse Events and Unanticipated Problems reporting.
  • Assures distribution of appropriate information between investigators, regulatory agencies and staff involved in implementation of research projects.
  • Maintains regulatory database as applicable. Maintains electronic and paper study files in accordance with local SOPs, sponsor and general industry standards ensuring documentation is complete, up to date, and audit ready.
  • Keeps the study team and supervisor informed of protocol related issues.
  • Participates in feasibility, implementation, and site initiation meetings, teleconferences, monitor visits, research audits and other onsite meetings as required.
  • Practices a high level of integrity and honesty in maintaining confidentiality.
  • Works proactively and collaboratively with other team members to streamline work and achieve mutual goals.
  • Attends all required meetings and conferences, contributes pertinent protocol information and uses information presented to develop an understanding of the hematology/oncology landscape, in order to more accurately assist in the preparation of submissions.
  • Plans and pursues activities to promote self development related to hematology/oncology and regulatory issues. Looks for opportunities to improve performance; manages time, work, and relationships effectively and efficiently.
  • Performs other job related duties as assigned.

Minimum Qualifications
  • Bachelor's degree.
  • Two years of relevant experience.

Department Specific Criteria
  • Two or more years of experience in regulatory affairs for clinical research at academic medical center or hospital with knowledge of clinical research practices and regulations.
  • Demonstrated knowledge of regulatory processes and applicable regulations.
  • Ability to manage regulatory aspects of multiple research projects.
  • Ability to establish and maintain cooperative and mutually supportive working relationships with faculty, administrators, staff, other campus units, sponsors, their representatives, and other business partners.
  • Knowledge and understanding of clinical research compliance, including OHRP, FDA and other federal regulations and requirements regarding human subjects research, including but not limited to GCPs and related ICH guidelines, informed consent, adverse event reporting and monitoring, and other human subjects research protection requirements.
  • Ability to serve as a resource to clinical investigators and staff.
  • Ability to manage shifting priorities in short time frames.

Preferred Qualifications
  • Certification in Clinical Research, SOCRA or other preferred.
  • Should have excellent oral and written communication skills.
  • Knowledge of medical/scientific terminology.
  • Excellent organization skills; ability to multi-task.
  • Strong computer skills including Microsoft Office Suite.
  • High sense of professional behavior and conduct and an ability to communicate with various levels of faculty and staff within Baylor College of Medicine and outside organization.

Work Authorization Requirement:
This position is not eligible for visa sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.
Requisition ID: 25474

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