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Part Time Icon Clinical Research Jobs (NOW HIRING)

IQVIA

Clinical Research Coordinator

Wichita, KS · On-site

$35 - $42/hr

On-site Schedule: Part-time, 24 hours per week About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

Our commitment to excellence in clinical research operations ensures the highest standards of ... This is a part-time position that requires working one week per month on-site according to the ...

ICON

T&M Dentist

Blue Bell, PA · On-site

Dentist ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation ...

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 advanced analytics, technology solutions, and clinical research services, dedicated to driving health ...

IQVIA

Clinical Research Coordinator

Cincinnati, OH

$35 - $42/hr

Clinical Research Coordinator - Cincinnati, OH Work Set-Up: On-site Schedule Weekly Hours: About ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

IQVIA

Clinical Research Coordinator

Linden, NJ

$35 - $42/hr

Clinical Research Coordinator - Somerset, NJ Work Set-Up: On-site Scheduled Weekly Hours: 40 Hours ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

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All JobsIcon Clinical Research JobsPart Time Icon Clinical Research Jobs

Part Time Icon Clinical Research information

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$13

$24

$40

How much do part time icon clinical research jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for part time icon clinical research in the United States is $24.09, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What is the difference between Part Time Icon Clinical Research vs Part Time Clinical Research Coordinator?

AspectPart Time Icon Clinical ResearchPart Time Clinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldRequires a bachelor's degree, often in health sciences, with some roles preferring certification
Work EnvironmentConducts clinical trials, often in research facilities or hospitalsManages daily trial activities, interacts with patients and research teams
Employer & Industry UsageUsed by pharmaceutical companies, research organizations, hospitalsCommonly employed by research sites, hospitals, and clinical trial sponsors

Part Time Icon Clinical Research and Part Time Clinical Research Coordinator roles share similar credentials and work environments, focusing on supporting clinical trials. The main difference lies in their specific responsibilities, with Icon roles often emphasizing trial support and coordination, while Clinical Research Coordinators handle more direct patient interactions and trial management tasks.

How much does Icon Clinical Research pay?

The salary for a Part Time Icon Clinical Research role varies depending on location, experience, and specific responsibilities, but typically ranges from $20 to $35 per hour. Compensation may also include benefits such as flexible schedules and opportunities for skill development in clinical trial management.

Which is better, IQVIA or ICON?

Both IQVIA and ICON are leading contract research organizations that provide clinical research services, including for roles like Part Time Icon Clinical Research. The choice between them depends on factors such as project scope, company culture, and specific job requirements. Both companies offer opportunities in clinical trial management, data analysis, and regulatory compliance, with differences in their client base and global presence.

Is ICON a good CRO to work for?

ICON is a global contract research organization known for offering opportunities in clinical research, including roles like Part Time Icon Clinical Research. Employees often cite competitive pay, flexible schedules, and a collaborative environment, though experiences can vary by location and role. Candidates should consider company culture, job responsibilities, and career growth prospects when evaluating employment at ICON.

How much does ICON pay CRAS?

The salary for Clinical Research Associates (CRAs) at ICON typically ranges from $70,000 to $100,000 annually, depending on experience, location, and specific project requirements. Part-time CRA roles may offer prorated pay based on hours worked and may include benefits such as flexible schedules and industry-standard tools for monitoring clinical trials.
More about Part Time Icon Clinical Research jobs
What cities are hiring for Part Time Icon Clinical Research jobs? Cities with the most Part Time Icon Clinical Research job openings:
What are the most commonly searched types of Icon Clinical Research jobs? The most popular types of Icon Clinical Research jobs are:
What states have the most Part Time Icon Clinical Research jobs? States with the most job openings for Part Time Icon Clinical Research jobs include:
What job categories do people searching Part Time Icon Clinical Research jobs look for? The top searched job categories for Part Time Icon Clinical Research jobs are:
Part Time Icon Clinical Research jobs near you
Infographic showing various Part Time Icon Clinical Research job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $50,108 per year, or $24.1 per hour.
Clinical Research Registered Nurse ( PT WeekDay)

Clinical Research Registered Nurse ( PT WeekDay)

Alcanza Clinical Research

Methuen, MA • On-site

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 6 days ago

Job description

Clinical Research Registered Nurse ( PT WeekDay)
Department: Operations
Employment Type: Part Time
Location: ActivMed Practices & Research | Methuen, MA
Reporting To: Katie Valcich
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Clinical Research Nurse works to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.
Key Responsibilities
Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
  • Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines:
    • Screening of patients for study enrollment;
    • Patient consents;
    • Patient follow-up visits;
    • Documenting in source clinic charts;
    • Entering data in EDC and answers queries;
    • Obtaining vital signs and ECGs;
    • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
    • Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.
    • Requesting and tracking medical record requests;
    • Updating and maintaining logs, chart filings;
    • Maintaining & ordering study specific supplies;
    • Scheduling subjects for study visits and conducts appointment reminders;
    • Building/updating source as needed;
    • Conducting monitoring visits and resolves issues as needed in a timely manner;
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;

o Filing SAE/Deviation reports to Sponsor and IRB as needed;
o Documenting and reporting adverse events;
o Reporting non-compliance to appropriate staff in timely manner;
o Maintaining positive and effective communication with clients and team members;
o Always practicing ALCOAC principles with all documentation;
  • Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
  • May set up, train and maintain all technology needed for studies.
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • Maintaining confidentiality of patients, customers and company information, and;
  • Performing all other duties as requested or assigned.

Skills, Knowledge and Expertise
Minimum Qualifications: A Bachelor's degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required. An active, unrestricted RN license, in state of work location, is required. BLS certification required. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm);
  • Proficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required.
  • Strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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