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Part Time Icon Clinical Research Jobs in Rochester, NY

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Part Time Icon Clinical Research information

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$13

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$40

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

As of Jul 26, 2026, the average hourly pay for part time icon clinical research in Rochester, NY is $23.77, according to ZipRecruiter salary data. Most workers in this role earn between $19.90 and $24.42 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.
What are popular job titles related to Part Time Icon Clinical Research jobs in Rochester, NY? For Part Time Icon Clinical Research jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Part Time Icon Clinical Research jobs in Rochester, NY look for? The top searched job categories for Part Time Icon Clinical Research jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Part Time Icon Clinical Research jobs? Cities near Rochester, NY with the most Part Time Icon Clinical Research job openings:
Part Time Icon Clinical Research jobs near you
Infographic showing various Part Time Icon Clinical Research job openings in Rochester, NY as of July 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $49,440 per year, or $23.8 per hour.
Human Subject Research Coordinator Trainee (PT) (ABCD Lab)

Human Subject Research Coordinator Trainee (PT) (ABCD Lab)

University of Rochester

Rochester, NY • On-site

$19.04 - $26.63/hr

Part-time

Posted 13 days ago

University Of Rochester rating

8.3

Company rating: 8.3 out of 10

Based on 185 frontline employees who took The Breakroom Quiz

123rd of 611 rated colleges and universities

Job description

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.
Job Location (Full Address):
220 Hutchison Rd, Rochester, New York, United States of America, 14620
Opening:
Worker Subtype:
Regular
Time Type:
Part time
Scheduled Weekly Hours:
32
Department:
400010 Neuroscience
Work Shift:
UR - Day (United States of America)
Range:
UR URG 104 H
Compensation Range:
$19.04 - $26.63
The referenced pay range represents the minimum and maximum compensation for this job. Individual annual salaries/hourly rates will be set within the job's compensation range, and will be determined by considering factors including, but not limited to, market data, education, experience, qualifications, expertise of the individual, and internal equity considerations.
Responsibilities:
The Human Subject Coordinator (HSRC) Trainee will assist with day-to-day implementation of the Adolescent Brain and Cognitive Development (ABCD) Study, a federally funded research study in the Cognitive Neurophysiology Lab. General protocol and directions are provided by a team of scientists at the ABCD Coordinating Center in San Diego, California. These protocols and directions are overseen by supervisory staff working at the Cognitive Neurophysiology Lab.
HSRC Trainee will assist with human subject consents for participation in neuroscience-related behavior and physiology research. This research will involve working with adolescents and their families but may also involve working with individuals with developmental disabilities, learning disorders, and diverse backgrounds. Under supervision, the HSRC Trainee will work with human subjects and carrying out study protocol.
The HSRC Trainee assists in subject consents and performing neurocognitive and psychological tests, as well as coordinating biologic sample collection. Study visits include conducting cognitive assessments, electronic surveys and interviews, collecting biological samples for genetic or drug testing, and guiding participants through MRI scans under supervision of a licensed technologist. The HSRC Trainee will utilize a variety of platforms for testing and data management, such as RedCap. All information, samples, and data that are collected must be stored and documented in accordance with IRB regulations.
Under supervision, the HSRC Trainee will be responsible for ensuring the comfort, privacy, and informed consent of human subjects during experimental procedures by explaining study information fully and following all protocols precisely. The HSRC Trainee will contribute to maintaining supplies and the cleanliness of the study.
ESSENTIAL FUNCTIONS
  • Plans and performs a variety of moderately-complex laboratory tests including MRI and cognitive/behavioral assessments on an iPad. Administers surveys and interviews research participants. Ensures research participants' adherence to protocol requirements. Assures proper setup and operation of specialized equipment. Understands, reviews, and documents all aspects of approved protocols, procedures, and standards for documentation and communication. Supports team members on the details of the protocol, including inclusion and exclusion criteria, informed consent procedures, and study activities.
  • Actively contributes to improving workflows, interacting with participants and parents.
  • Assists in other study based delegations and management.

MINIMUM EDUCATION & EXPERIENCE
  • Associate's degree required.
  • Experience as a Phlebotomist preferred. No previous experience required

KNOWLEDGE, SKILLS AND ABILITIES
  • Excellent interpersonal and customer service skills preferred.
  • Strong organizational and communication skills, including written communication preferred.
  • Ability to collect observational data, attention to detail, and competence with lab equipment preferred.
  • Knowledge of word processing and other Microsoft Office tools, such as Excel preferred.
  • Knowledge with Google based tools, such as Google Sheets preferred
  • Experience with data collection software (i.e. Redcap) preferred

LICENSES AND CERTIFICATIONS
  • CITI training certifications preferred

The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University's Mission to Learn, Discover, Heal, Create - and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.

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