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Clinical Trial Associate Part Time 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 ...

IQVIA

Clinical Research Coordinator

Philadelphia, PA · Remote

$35 - $42/hr

On-site Employment Type: Part-time - 24 Hours per Week About IQVIA IQVIA is a global leader in ... Coordinate day-to-day clinical trial activities while ensuring compliance with GCP, protocol, and ...

ECN Operating LLC

Physician - Rheumatologist

Scottsdale, AZ · On-site

$276K - $356K/yr

This is a part time/per diem position with a unique opportunity to contribute to the advancement of ... Provide medical oversight for clinical trial participants, including safety assessments, adverse ...

Ossium Health

Clinical Operations Intern

San Francisco, CA · On-site

$20 - $28/hr

This role reports to Associate Director, Clinical Operations. Required Qualifications * Currently ... Support the team with clinical trial activities across different programs * Assist with maintaining ...

ECN Operating LLC

Physician - Dermatology

Tucson, AZ

This is a part time/per diem position with a unique opportunity to contribute to the advancement of ... Provide medical oversight for clinical trial participants, including safety assessments, adverse ...

ECN Operating LLC

Physician - Internist

Chandler, AZ · On-site

This is a part time/per diem position with a unique opportunity to contribute to the advancement of ... Provide medical oversight for clinical trial participants, including safety assessments, adverse ...

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Clinical Trial Associate Part Time information

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How much do clinical trial associate part time jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for clinical trial associate part time in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Trial Associate Part Time, and why are they important?

To thrive as a Clinical Trial Associate Part Time, you need a strong understanding of clinical research processes, regulatory compliance, and attention to detail, often supported by a life sciences degree or relevant experience. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Excellent organizational skills, proactive communication, and teamwork are crucial soft skills for managing study documentation and supporting trial operations. These competencies ensure accurate trial execution, regulatory adherence, and smooth coordination within clinical research teams.

What does a Clinical Trial Associate Part Time do?

A Clinical Trial Associate (CTA) Part Time supports the administrative aspects of clinical research studies on a reduced schedule. Their responsibilities include organizing trial documentation, assisting with regulatory submissions, maintaining study files, and coordinating communication between research teams and clinical sites. Part-time CTAs may work in hospitals, research organizations, or pharmaceutical companies, helping ensure that trials comply with protocols and regulatory requirements. This role is ideal for individuals seeking flexible work arrangements while contributing to important medical research.

What are some typical responsibilities of a part-time Clinical Trial Associate, and how do they balance workload with limited hours?

Part-time Clinical Trial Associates often handle essential tasks such as managing trial documentation, assisting with regulatory submissions, and supporting study coordinators. Balancing workload with limited hours requires strong organizational skills and effective communication with the team to prioritize tasks and ensure timely completion. They may also attend meetings, help maintain trial databases, and coordinate with investigators and site staff. Many organizations support flexible scheduling and clear task delegation to help part-time associates integrate seamlessly while meeting project deadlines.

What is the difference between Clinical Trial Associate Part Time vs Clinical Trial Coordinator?

AspectClinical Trial Associate Part TimeClinical Trial Coordinator
CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, experience in clinical research
Work EnvironmentPart-time, office and clinical sitesFull-time, primarily office-based with site visits
Employer & IndustryPharmaceutical companies, CROs, biotech firmsResearch institutions, hospitals, pharmaceutical companies
Common Search & ComparisonYesYes

The main difference between a Clinical Trial Associate Part Time and a Clinical Trial Coordinator lies in their work hours and scope. The part-time associate typically works fewer hours and focuses on specific trial tasks, while the coordinator manages broader trial activities full-time. Both roles require similar educational backgrounds and are integral to clinical research teams.

What cities are hiring for Clinical Trial Associate Part Time jobs? Cities with the most Clinical Trial Associate Part Time job openings:
What are the most commonly searched types of Clinical Trial Part Time jobs? The most popular types of Clinical Trial Part Time jobs are:
What states have the most Clinical Trial Associate Part Time jobs? States with the most job openings for Clinical Trial Associate Part Time jobs include:
Clinical Trial Associate Part Time jobs near you
Infographic showing various Clinical Trial Associate Part Time job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.
Clinical Affairs Manager (Part-Time)

Clinical Affairs Manager (Part-Time)

Aegis Ventures

Remote

$135 - $175/hr

Full-time, Part-time

Medical

Posted 19 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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