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Clinical Trial Associate Part Time Jobs (NOW HIRING)

Dana-Farber Cancer Institute, Inc.

Ensures timely facilitation of trial assessments per protocol and collection of protocol related ... Bachelor's Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience ...

Dana-Farber Cancer Institute, Inc.

Ensures timely facilitation of trial assessments per protocol and collection of protocol related ... Bachelor's Degree or 1 year of Dana-Farber Associate Clinical Research Coordinator experience ...

Adams Clinical

Lead Dosing Session Monitor

Boston, MA · Hybrid

$65 - $76/hr

Join Us in Shaping the Future of Clinical Research   Adams Clinical is a leading clinical trial ... This is a part-time role with 24 guaranteed hours per week. * Therapists are expected to maintain ...

Adams Clinical

Lead Dosing Session Monitor

New York, NY · Hybrid

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research   Adams Clinical is a leading clinical trial ... This is a part-time role with 24 guaranteed hours per week. * Therapists are expected to maintain ...

Adams Clinical

Lead Dosing Session Monitor

Boston, MA · On-site

$65 - $76/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... Job Role We are seeking a Part-Time Psychedelic Dosing Monitor / Therapist to support clinical ...

Adams Clinical

Lead Dosing Session Monitor

New York, NY · On-site

$60 - $70/hr

Join Us in Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site ... Job Role We are seeking a Part-Time Psychedelic Dosing Monitor / Therapist to support clinical ...

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Clinical Trial Associate Part Time information

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$70

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

As of Jul 14, 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.
Physician - Clinical Trials - MD/DO

Physician - Clinical Trials - MD/DO

Headlands Research

Little Rock, AR • On-site

Full-time, Part-time

Re-posted 29 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
Join Us in Improving Lives through Clinical Research
At Headlands Research, we're not just building a clinical trial network; we are working to bring clinical trials to underserved communities and new treatments to market. Picture this: an exceptional family of next-generation clinical trial sites, where cutting-edge technology meets unparalleled support services, and participant engagement reaches new heights. Established in 2018, we've rapidly grown to operate 20+ clinical trial sites across the US and Canada, with ambitious plans for expansion on the horizon.
Championing Diversity in Clinical Trials
Diversity isn't just a checkbox for us-it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.
The Role of a Lifetime
Are you ready to make a difference? We're seeking an experienced Principal Investigator or Sub-Investigator to help us grow a new clinical research site in the Little Rock area. Whether you're a seasoned Family Medicine physician or a specialist in Endocrinology, Neurology, or other area of medicine, your passion for improving patient outcomes is what matters most. If you have previous experience as an Investigator for clinical research trials, we want to talk with you. We're flexible-we're open to part-time or full-time commitments with flexible schedules.
Why Join Us?
  • Flexible Schedule: Work on your terms, with a schedule that fits your life.
  • Unlimited Potential: The sky's the limit. We're open to up to 40 hours per week, allowing you to maximize your impact.
  • Dynamic Team Environment: You'll help Headlands Research build a diverse and talented team of clinical research coordinators, research assistants, physicians, advanced providers, and patient recruitment specialists. With ample support and a culture of collaboration, you'll thrive in an environment where your contributions truly make a difference. A high level of professionalism is a key differentiator at Headlands.

Responsibilities:
  • Lead and oversee clinical trials conducted at Headlands Research sites, ensuring compliance with protocol requirements, regulatory standards, and ethical guidelines.
  • Provide leadership and mentorship to site staff, fostering a culture of inclusivity, diversity, and professionalism within the research team.
  • Participate in investigator meetings and educational initiatives to stay updated on advancements in clinical research and diversity initiatives.
  • Obtain IRB approval for study initiation and any protocol modifications.
  • Oversee subject safety, trial conduct compliance, and the informed consent process.
  • Communicate effectively with stakeholders including sponsors, monitors, regulators, and research network leadership.
  • Provide ongoing training and support to research staff.

Requirements:
  • Previous experience as a Principal Investigator or Sub-Investigator for clinical research trials required.
  • Active and unencumbered license to practice as an MD or DO within the state of Arkansas required.
  • Must be board-certified or board-eligible.
  • Excellent communication and leadership skills, with the ability to collaborate effectively with sponsors, research teams, and external stakeholders.
  • Familiarity with regulatory requirements, Good Clinical Practice (GCP) guidelines, and industry best practices in clinical research.
  • Strong organizational skills and attention to detail, with the ability to manage multiple projects simultaneously in a fast-paced environment.

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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