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Part Time Fda Regulatory Jobs (NOW HIRING)

Aegis Ventures

Clinical Affairs Manager (Part-Time)

$135 - $175/hr

About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and ... Support FDA regulatory pathway including Q-sub preparation and clinical trial protocols * Oversee ...

Bizzell Group

Central North Carolina (Triangle Region) Job Type: Part-Time, Temporary Headquarters: New ... This position plays a critical role in supporting federal and state regulatory enforcement by ...

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 ...

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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.
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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.
Clinical Affairs Manager (Part-Time)

Clinical Affairs Manager (Part-Time)

Aegis Ventures

Remote

$135 - $175/hr

Full-time, Part-time

Medical

Posted 10 days ago

Job description

About Aegis Ventures
Aegis Ventures partners with entrepreneurs and industry leaders to launch and scale transformative companies in digital health and artificial intelligence. Our platform brings together market-shaping ideas, growth capital, and ambitious individuals to solve major societal problems. With a focus on innovations in healthcare, Aegis has launched four successful portfolio companies in partnership with Northwell Health and recently announced the Digital Consortium to co-develop, invest in, and launch new companies.
About the Company
Wavelet Medical aims to revolutionize fetal health monitoring to eliminate preventable brain injuries at birth, reduce unnecessary C-sections, and improve outcomes for mothers and their babies. While traditional fetal heart rate monitoring is widely used, it has not meaningfully reduced brain injuries and has been linked to increased C-section rates.
Wavelet is building the first non-invasive electroencephalography (EEG) system to measure fetal brain activity during pregnancy and labor. Our technology combines novel sensing hardware with advanced signal processing and machine learning to extract clinically meaningful EEG signals from complex biological noise-enabling earlier, more accurate assessment of fetal neurological health without compromising maternal or fetal safety. This approach supports better clinical decision-making and healthier outcomes during childbirth.
We are a venture-backed, early-stage medtech company advancing toward FDA clearance of a Class II medical device.
About the Job
As the Clinical Affairs Manager (Part-Time), you will lead clinical affairs and drive adoption of our breakthrough fetal monitoring technology. This role will be critical in bridging our innovative technology with clinical practice, supporting regulatory approval, and establishing hospital partnerships. This role will be up to 25 hours a month.
This is a part-time position (approximately 25 hours per month) and is remote within the U.S., with periodic travel required to clinical sites. We have a preference for candidates based in major metropolitan areas with access to academic medical centers.
What You'll Do
  • Clinical Development & Validation
    • Lead clinical study design and execution across multiple hospital sites
    • Manage relationships with clinical investigators and hospital administrators
    • Support FDA regulatory pathway including Q-sub preparation and clinical trial protocols
    • Oversee clinical data collection and analysis for regulatory submissions
  • Hospital Partnerships & Implementation
    • Establish and maintain relationships with OB/GYN departments and L&D units
    • Guide clinical workflow integration and user experience optimization
    • Support hospital IRB processes and vendor vetting procedures
    • Lead clinical training and education programs for adoption
  • Cross-Functional Collaboration
    • Work closely with engineering team on device usability and clinical requirements
    • Partner with regulatory consultants on FDA strategy and submissions
    • Collaborate with algorithm team on clinical validation of EEG analysis
    • Interface with business development on hospital partnership negotiations
What You'll Need
  • Clinical Background
    • Advanced degree (MSN, MD, or PhD) with 5-10 years experience
    • Direct experience in obstetrics, neonatal care, or women's health preferred
    • Understanding of fetal monitoring technologies and labor & delivery workflows preferred
    • Experience with clinical research, preferably medical device studies
  • Regulatory & Research Experience
    • Knowledge of FDA medical device regulations (510k, PMA pathways)
    • Experience with clinical trial design, IRB processes, and GCP compliance
    • Track record of successful regulatory submissions or clinical study management
    • Understanding of biostatistics and clinical data analysis
  • Industry Experience
    • Medical device or healthcare technology background strongly preferred
    • Experience working with hospital systems and clinical decision-makers
    • Understanding of healthcare reimbursement and adoption challenges
    • Familiarity with quality systems and ISO 13485 requirements
What We Offer
  • Remote-first culture with periodic team gatherings
  • Healthcare benefits and competitive compensation
  • Equity participation in breakthrough medical technology
  • Opportunity to directly impact maternal and neonatal outcomes globally
  • Collaboration with world-class clinical researchers at Yale, USC, and international partners
Salary Range
  • $135/hour - $175/hour, depending on experience and alignment with role expectations.

Aegis Ventures is a proud Equal Opportunity Employer - we recruit, train, compensate and promote our team members based on qualifications. We encourage you to apply regardless of your race, religion, national origin, sex, gender identity, sexual orientation, disability, age, veteran status, or any other applicable legally protected characteristics.

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