ZipRecruiter

Log In

2

Part Time Fda Regulatory Jobs (NOW HIRING)

North Memorial Health

Manager, Regulatory

Robbinsdale, MN · On-site

$50.64 - $63.29/hr

Most part-time and all full-time positions are eligible for benefits. * Health & Welfare Benefit ... CMS, MN Department of Health, OSHA, FDA, DNV, etc. This role will lead and collaborate on system ...

next page

Showing results 1-20

All JobsPart Time Fda Regulatory Jobs

Part Time Fda Regulatory information

See salary details

$15

$34

$145

How much do part time fda regulatory jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for part time fda regulatory in the United States is $34.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $26.20 per hour, depending on experience, location, and employer.

What is the difference between Part Time Fda Regulatory vs Part Time Fda Compliance Specialist?

AspectPart Time Fda RegulatoryPart Time Fda Compliance Specialist
Required CredentialsRegulatory Affairs Certification, Bachelor's in Life SciencesRegulatory Affairs Certification, Bachelor's in Life Sciences
Work EnvironmentRegulatory departments, offices, labsQuality assurance, regulatory departments, offices
Employer & Industry UsageMedical device, pharmaceutical companiesMedical device, pharmaceutical companies
Common Search & ComparisonYesYes

Part Time Fda Regulatory and Part Time Fda Compliance Specialist roles often overlap in credentials, work environment, and industry. Both require similar certifications and are found in regulated industries like pharmaceuticals and medical devices. The main difference lies in focus: Fda Regulatory roles emphasize navigating FDA regulations and submissions, while Compliance Specialists focus on ensuring ongoing adherence to those regulations within organizations.

What are the most common challenges faced by part-time FDA Regulatory professionals, and how can they be managed?

Part-time FDA Regulatory professionals often face the challenge of staying up-to-date with rapidly changing regulations while managing limited working hours. Balancing multiple projects, meeting tight submission deadlines, and maintaining clear communication with cross-functional teams can also be demanding. To overcome these challenges, it's important to set clear priorities, use efficient workflow tools, and stay proactive about regulatory updates. Open communication with supervisors and colleagues helps ensure alignment and smooth information flow, even with a part-time schedule.

What does a Part Time FDA Regulatory professional do?

A Part Time FDA Regulatory professional helps organizations comply with regulations set by the U.S. Food and Drug Administration (FDA). Their responsibilities often include reviewing documentation, preparing submissions, and advising on compliance for products such as drugs, medical devices, food, or cosmetics. Working part-time, they may focus on specific projects or provide ongoing support to regulatory teams. Their expertise ensures that products meet all necessary legal and safety standards before and after they reach the market.

What are the key skills and qualifications needed to thrive as a Part Time FDA Regulatory professional, and why are they important?

To thrive as a Part Time FDA Regulatory professional, you need strong knowledge of FDA regulations, compliance standards, and documentation practices, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission systems, such as eCTD, and certifications like RAC (Regulatory Affairs Certification) are highly valued. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for managing complex regulatory processes and collaborating with cross-functional teams. These competencies ensure that products meet legal requirements and reach the market efficiently while maintaining compliance and minimizing risk.
More about Part Time Fda Regulatory jobs
What cities are hiring for Part Time Fda Regulatory jobs? Cities with the most Part Time Fda Regulatory job openings:
What are the most commonly searched types of Fda Regulatory jobs? The most popular types of Fda Regulatory jobs are:
What states have the most Part Time Fda Regulatory jobs? States with the most job openings for Part Time Fda Regulatory jobs include:
What job categories do people searching Part Time Fda Regulatory jobs look for? The top searched job categories for Part Time Fda Regulatory jobs are:
Part Time Fda Regulatory jobs near you
Infographic showing various Part Time Fda Regulatory job openings in the United States as of May 2026, with employment types broken down into 73% Full Time, 26% Part Time, and 1% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.

Clinical Research Coordinator - Part Time

GULF COAST HEART AND VASCULAR LLC

Panama City, FL • On-site

$20.75 - $27.50/hr

Part-time

Posted 10 days ago

Job description

Position Overview

We are seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to join our team. The CRC will be responsible for the day-to-day coordination and execution of clinical trials, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP).
This is an excellent opportunity for someone who thrives in a startup environment and is eager to grow with an organization.
Key Responsibilities

  • Coordinate and manage clinical trials from start-up through close-out
  • Screen, recruit, and consent study participants
  • Schedule and conduct study visits per protocol
  • Collect, process, and ship laboratory specimens
  • Accurately document study data in source documents and electronic data capture (EDC) systems
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, and study protocols
  • Maintain regulatory binders and essential documents
  • Communicate with sponsors, CROs, and study monitors
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Track study timelines, enrollment, and patient follow-up
  • Report adverse events and protocol deviations appropriately
Qualifications

Required:

  • Bachelors degree in health sciences, biology, or related field (or equivalent experience)
  • 1+ years of clinical research experience (or strong clinical background willing to train)
  • Knowledge of GCP and FDA regulations
  • Strong organizational and multitasking skills
  • Excellent communication and interpersonal skills
  • Ability to work independently in a fast-paced environment
Preferred:

  • Experience in cardiology
  • Experience with EDC systems
  • Phlebotomy and/or clinical skills
  • ACRP or SOCRA certification (or willingness to obtain)
What We Offer

  • Competitive salary based on experience
  • Opportunity for career growth
  • Direct exposure to sponsors and leadership
  • Flexible and collaborative work culture