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Full Time Human Subject Research Jobs (NOW HIRING)

University of Rochester

$21.78 - $30.53/hr

Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400133 ... Coordinates the activities associated with human subject research. ESSENTIAL FUNCTIONS

University of Rochester

$25.14 - $35.24/hr

Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400049 Med M&D-Pulmnry/Crit ... Coordinates human subject research activities, which may include multiple site human subject ...

University of Rochester

$61K - $85K/yr

Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400098 General Neurology Unit ... Oversees human subject research activities for single or multiple sites. Develops, implements, and ...

University of Rochester

$21.78 - $30.53/hr

Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400081 General Pediatrics Work ... GENERAL PURPOSE The Human Subject Research Specialist I (HSRS I) plays a vital role in contributing ...

University of Rochester

$21.78 - $30.53/hr

Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400981 Neuro-Ctr Health & Tech ... the Human Subject Research Coordinator Trainee program required. * 1- 2 years' experience in ...

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Full Time Human Subject Research information

What are the key skills and qualifications needed to thrive in full time human subject research?

To thrive in Full Time Human Subject Research, you need a solid background in scientific methodology, ethical research practices, and often a degree in a relevant field such as psychology, biology, or public health. Familiarity with data collection tools, statistical software (like SPSS or R), and Institutional Review Board (IRB) protocols is typically required. Exceptional attention to detail, strong interpersonal skills, and clear communication help ensure accurate data collection and ethical participant interactions. These skills and qualities are crucial for producing valid research outcomes while safeguarding participant rights and well-being.

What is a full time human subject researcher?

A Full Time Human Subject Researcher is a professional who conducts scientific studies involving human participants. Their work typically includes designing research protocols, recruiting and monitoring subjects, collecting data, and ensuring all research is conducted ethically and in compliance with regulations. They may work in academic, clinical, or private research settings and often collaborate with other scientists and medical professionals. The goal is to advance knowledge in fields such as medicine, psychology, or public health, while prioritizing the safety and rights of human subjects.

What are the typical challenges faced by professionals in full time human subject research roles?

Professionals working in full-time human subject research often face challenges such as recruiting and retaining participants, ensuring strict compliance with ethical guidelines and institutional review board (IRB) protocols, and managing sensitive data securely. Balancing administrative tasks with hands-on research activities can also be demanding, as can coordinating with multidisciplinary teams including clinicians, statisticians, and regulatory staff. Strong organizational skills and adaptability are key to successfully navigating these complexities while maintaining the integrity of the study.

What is the difference between Full Time Human Subject Research vs Full Time Clinical Research Coordinator?

AspectFull Time Human Subject ResearchFull Time Clinical Research Coordinator
CredentialsOften requires a bachelor's degree in health sciences, psychology, or related fields; certifications like CITI are commonTypically requires a bachelor's degree; certifications like CITI or CCRP are advantageous
Work EnvironmentResearch institutions, universities, hospitals conducting human subject studiesClinical trial sites, hospitals, research centers managing patient studies
Employer & IndustryAcademic, government, or private research organizationsPharmaceutical companies, hospitals, clinical research organizations

Both roles involve working with human subjects in research settings, but Full Time Human Subject Research often focuses on designing and analyzing studies, while Clinical Research Coordinators manage day-to-day trial operations. Understanding these differences helps job seekers identify the right career path in clinical research.

More about Full Time Human Subject Research jobs
What cities are hiring for Full Time Human Subject Research jobs? Cities with the most Full Time Human Subject Research job openings:
What are the most commonly searched types of Human Subject Research jobs? The most popular types of Human Subject Research jobs are:
What states have the most Full Time Human Subject Research jobs? States with the most job openings for Full Time Human Subject Research jobs include:
What job categories do people searching Full Time Human Subject Research jobs look for? The top searched job categories for Full Time Human Subject Research jobs are:
Full Time Human Subject Research jobs near you
Infographic showing various Full Time Human Subject Research job openings in the United States as of August 2026, with employment types broken down into 55% Full Time, 27% Part Time, 1% Temporary, and 17% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution.

Human Subject Research Spec II

University of Rochester

Rochester, NY • On-site

$25.14 - $35.24/hr

Full-time

Re-posted yesterday

University Of Rochester rating

8.3

Company rating: 8.3 out of 10

Based on 186 frontline employees who took The Breakroom Quiz

125th of 617 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:
Full time
Scheduled Weekly Hours:
40
Department:
400075 Breastfeeding & Lactation Med
Work Shift:
UR - Day (United States of America)
Range:
UR URG 108 H
Compensation Range:
$25.14 - $35.24
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:
Coordinates human subject research activities, which may include multiple site human subject studies in the field of Breastfeeding and Lactation Medicine. May provide training on federal, state, sponsor and/or institutional regulations, policies and practices related to human subject research. May supervisor others. This position involves working with breastfeeding and lactating families, managing study documents and workflow, collecting and processing study samples, and managing regulatory aspects of clinical research studies.
ESSENTIAL FUNCTIONS
  • Oversees and coordinates human subject research activities for single or multiple sites. Develops, implements and evaluates recruitment strategies, information and data systems and study management systems. Participates in the planning, development and implementation of study design, budgets, protocols, consent forms, processes and policies that may include multiple therapeutic areas. Participates in the development, review and approval of case report forms (CRFs) and study-specific procedure manuals and documents.
  • Represents sites, providers, study team, patients, study participants and the University to develop, monitor and maintain working relationships, positive communications and effective results with regard to the coordination of human subject studies. Supports the contacts and relationships between and among Principal Investigator (PI), research staff, study sites and sponsoring and regulatory agencies.
  • Develops, implements and monitors systems and methods to ensure quality, safety, efficiency and consistency in the processing of human subject research data. Reviews study progress, including data, finances, documentation and reporting deliverables. Designs, develops, implements, monitors and manages systems and procedures for the purpose of tracking study progression.
  • Ensures compliance with all applicable regulatory and institutional requirements and standards. Ensures the integrity and security of all study data at all times. Initiates, monitors and ensures that all protocol activities are standardized across study sites. Implements immediate and appropriate corrective action when inconsistency of activities is identified.
  • Trains research coordinators and other staff on activities associated with conducting human subject research specific to study protocols and generally in compliance with Good Clinical Practice (GCPs) guidelines and sponsor requirements.
  • Directs the activities of subordinate staff and relevant others to gather, compile and analyze study information.
  • Coordinates and monitors financial data for budget and variance reporting and for compliance with all institutional requirements for adequate system controls.
  • Keeps current with all federal, state, sponsor and institutional policies and laws, standard operating procedures and guidelines. Demonstrates accountability for continuous learning in accordance with GCP guidelines. Keeps current with industry standards, best practices and trends in therapeutic areas relevant to research studies and designs. Implements and monitors resulting study changes.
  • Other duties as assigned

MINIMUM EDUCATION & EXPERIENCE
  • Bachelor's degree and 2 years of experience in human subject research coordination required (3 years preferred).
  • Or equivalent combination of education and experience
  • Experience as Human Subject Research Coordinator I preferred
  • Experience working with perinatal populations and/or infants preferred
  • If applicable, department specific experience required
  • Experience as a Phlebotomist preferred

KNOWLEDGE, SKILLS AND ABILITIES
  • Word processing and data analysis software required

LICENSES AND CERTIFICATIONS
  • SOCRA - Certification In Clinical Research upon hire preferred
  • Association of Clinical Research Professionals (ACRP) upon hire 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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