ZipRecruiter

Log In

2

Clinical Trial Associate Part Time Jobs (NOW HIRING)

IQVIA

Clinical Trial Nurse

Fargo, ND

$50 - $60/hr

Clinical Trial Nurse (Per Diem) - Fargo, ND Work Setting: Local Travel - In-Home Patient Visits Job ... It is an excellent opportunity for PRN, part-time, or experienced nurses seeking supplemental ...

next page

Showing results 1-20

All JobsClinical Trial Associate JobsClinical Trial Associate Part Time Jobs

Clinical Trial Associate Part Time information

See salary details

$17

$39

$70

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

As of Aug 8, 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.

Is a clinical trial associate a good career?

A clinical trial associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical studies. It offers opportunities for career growth, skill development in regulatory compliance and data management, and often requires attention to detail and certification in Good Clinical Practice (GCP).
More about Clinical Trial Associate Part Time jobs
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:
What job categories do people searching Clinical Trial Associate Part Time jobs look for? The top searched job categories for Clinical Trial Associate Part Time jobs are:
Clinical Trial Associate Part Time jobs near you
Infographic showing various Clinical Trial Associate Part Time job openings in the United States as of August 2026, with employment types broken down into 5% Full Time, and 95% Part Time. Highlights an 95% In-person, and 5% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Clinical Research Associate - Part Time

Saint Peter's Healthcare System

New Brunswick, NJ • On-site

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement

Re-posted 2 days ago

Saint Peter's University Hospital rating

8.0

Company rating: 8.0 out of 10

Based on 14 frontline employees who took The Breakroom Quiz

134th of 1,055 rated hospitals

Job description

Clinical Research Associate - Part Time
MFM Clinical Study Grant
The Clinical Research Associate - Part Time will:
  • Serve as the organizational appointee for assigned MFM research projects, maintaining the relationship and oversight of study procedures.
  • Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and updating the Informed Consent Form with CIRB Boilerplate, Completion of Institutional Review Board (IRB) modifications with supporting documentation.
  • Maintain oversight of designated research project study activities including performing the following functions: Subject recruitment, Consenting and Enrollment/Randomization, Perform study procedures/assessments in accordance with clinical trial guidelines, Complete Data Entry into Case Report Forms and Query Resolution, Process/Ship Specimens per trial requirements, Maintain Regulatory files including delegation logs, FDA form 1572, training logs and other trial documents in compliance with federal and local regulations, Process IRB amendments, annual renewals, closures, etc, Attend regular meetings with members of the project at partnering institutions and sponsors to report on study progress.
  • Maintain financial records including Accounts Receivable Report, Check remittance with back-up details and assist with the annual A-133 audit.
  • Serve as a liaison between investigators, research staff, hospital staff, the IRB and sponsors.
  • Maintain and utilize research's Clinical Trial Management System (CTMS).
  • Maintain strict patient confidentiality including restricted access to clinical trial files.
  • Attend and participate in research meetings and report on study progress.
  • Perform other tasks as assigned by leadership.
  • Comply with all SPUH policies, procedures, objectives, quality assurance, safety, environmental and infection controls.

Requirements:
  • Bachelor's Degree in science or healthcare field preferred.
  • Two years of experience in healthcare and/or research.
  • Ability to work independently as well as in a team environment.
  • Proficient in Microsoft Office Suite.
  • Certified Clinical Research Professional (CCRP) or other similar research accreditation preferred.
  • Previous Phlebotomy experience or certification preferred.

Salary Range: 24.33 - 38.93 USD
We offer competitive base rates that are determined by many factors, including job-related work experience, internal equity, and industry-specific market data. In addition to base salary, some positions may be eligible for clinical certification pay and shift differentials.
The salary range listed for exempt positions reflects full-time compensation and will be prorated based on employment status.
Saint Peter's offers a robust benefits program to eligible employees that will support you and your family in working toward achieving and maintaining secure, healthy lives now and into the future. Benefits include medical, dental, and vision insurance; savings accounts, voluntary benefits, wellness programs and discounts, paid life insurance, generous 401(k) match, adoption assistance, back-up daycare, free onsite parking, and recognition rewards.
You can take your career to the next level by participating in either a fully paid tuition program or our generous tuition assistance program. Learn more about our benefits by visiting our site at Saint Peter's.

What Saint Peter's University Hospital employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply