ZipRecruiter

Log In

2

Part Time Icon Clinical Research Jobs (NOW HIRING)

Angel City VA

Clinical Research Assistant

Los Angeles, CA · On-site

Title: Part time Clinical Research assistant Job Summary: The Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while ...

Apply Early

next page

Showing results 1-20

All JobsPart Time Icon Clinical Research Jobs

Part Time Icon Clinical Research information

See salary details

$13

$24

$40

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

As of Jul 3, 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 June 2026, with employment types broken down into 2% As Needed, and 98% Full Time. 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 Principal Investigator - Neurologist

Clinical Research Principal Investigator - Neurologist

Alcanza Clinical Research

Katy, TX • On-site

$42K - $43K/yr

Part-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago

Job description

Clinical Research Principal Investigator - Neurologist
Department: Operations
Employment Type: Part Time
Location: Olympus - Katy, TX
Reporting To: Alberto Blanco
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 Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Key Responsibilities
Essential Job Duties:
  • Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
  • Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
  • Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
  • Participates and engages in successful delivery and retention of study participants.
  • Interacts positively and collaboratively with sponsors, clients and team members.
  • Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
  • Actively involved in protocol training for staff.
  • Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
  • Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.

Skills, Knowledge and Expertise
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required. Clinical Research experience is required. Board certification in neurology is required.
Required Skills:
  • Clinical procedures based on area of specialty.
  • Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational skills, attention to detail, and math proficiency.
  • Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
  • Must possess a high degree of urgency, self-motivation, integrity and dependability.
  • Ability to work independently to 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.

Apply