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Part Time Fda Regulatory Jobs (NOW HIRING)

System One Holdings, LLC

Biostatistician

Jersey City, NJ · On-site

$60 - $65/hr

... FDA regulations and industry standards. This is a part-time consulting position ideal for a biostatistician with experience supporting clinical research within the medical device or healthcare ...

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Part Time Fda Regulatory information

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$15

$34

$145

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

As of Jul 6, 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 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 June 2026, with employment types broken down into 100% Part Time. Highlights an 89% In-person, 2% Hybrid, and 9% Remote job distribution, with an average salary of $71,960 per year, or $34.6 per hour.
Part Time Clinical Research Coordinator

Part Time Clinical Research Coordinator

SerenaGroup

Monroeville, PA • On-site

$53K - $58K/yr

Part-time

Posted 22 days ago

Job description

Job Type
Part-time
Description
The Clinical Research Coordinator (CRC) at SerenaGroup plays a critical role in the execution of clinical trials focused on advanced wound care and hyperbaric medicine. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory guidelines, and supporting high-quality patient care and data integrity throughout the study lifecycle.
The CRC will work collaboratively with Principal Investigators, Clinical Trial Leads, sponsors, and cross-functional teams to ensure studies are conducted efficiently, ethically, and in alignment with SerenaGroup's commitment to evidence-based care and improved patient outcomes.
Key Responsibilities
Study Coordination & Execution
  • Coordinate and manage day-to-day clinical trial activities from study start-up through close-out
  • Schedule and conduct study visits in accordance with protocol requirements
  • Ensure proper informed consent is obtained and documented for all study participants
  • Maintain accurate and up-to-date study documentation, including regulatory binders and source documents

Patient Care & Engagement
  • Identify, recruit, and screen eligible patients for clinical trials
  • Educate patients on study protocols, procedures, and expectations
  • Monitor patient safety and report adverse events in accordance with regulatory requirements

Data Management & Compliance
  • Accurately collect, record, and enter study data into electronic data capture (EDC) systems
  • Perform source data verification (SDV) and ensure data integrity and completeness
  • Ensure compliance with FDA regulations, ICH-GCP guidelines, and SerenaGroup SOPs

Collaboration & Communication
  • Serve as a liaison between investigators, sponsors, CROs, and internal teams
  • Support monitoring visits, audits, and regulatory inspections
  • Communicate effectively with cross-functional teams to ensure study milestones are met

Qualifications
Education & Experience
  • Bachelor's degree in life sciences, healthcare, or related field preferred
  • 1-3 years of experience in clinical research or healthcare setting (wound care experience a plus)
  • Experience working with clinical trial protocols and regulatory requirements preferred

Skills & Competencies
  • Strong organizational and time management skills
  • High attention to detail and accuracy in documentation
  • Excellent interpersonal and communication skills
  • Ability to manage multiple studies and priorities in a fast-paced environment
  • Proficiency in EDC systems and Microsoft Office Suite

Preferred Qualifications
  • Certification as a Clinical Research Coordinator (e.g., ACRP or SOCRA)
  • Experience in wound care, hyperbaric medicine, or related therapeutic areas
  • Familiarity with clinical trial start-up and regulatory submissions

Salary Description
$53,000-$58,000

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