Top 49 Clinical research associate Jobs in Brighton Ny

Clinical Research Coordinator
System One —Rochester, NY
- $26 - $30 an hour
- Contract
- CPR Certification
- BLS Certification
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
7d
Clinical Research Data Spec I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- University
- Organizational skills
- Experience equivalent to degree accepted
10d
Clinical Research Coordinator
ALLIANCE CLINICAL LLC —Rochester, NY
- $28 - $30 an hour
- Temporary
- CPR Certification
- Microsoft Excel
- BLS Certification
Quick Apply
7d
Wilmot Cancer Center - Clinical Trials Office - Clinical Research Nurse - Registered Nurse 2, Outpatient
University of Rochester —Rochester, NY
- $38.76 - $52.33 an hour
- Full-time
- Nursing
- Word processing
- Outpatient experience
Clinical Research Spec II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Mid-level
- Clinic
- Bachelor's degree
Human Subject Research Spec II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Word processing
- Mid-level
- University
Clinical Research Regulatory Specialist II
University of Rochester —Rochester, NY
- $24.91 - $34.87 an hour
- Day shift
- Mid-level
- Office
- University
Human Subject Research Spec I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Word processing
- University
- Associate's degree
Research RN
University of Rochester —Rochester, NY
- $35.35 - $47.72 an hour
- Full-time
- Nursing
- RN License
- Word processing
5d
Infusion Nurse
Rochester Skin Lymphoma Center —Fairport, NY
- $50 - $80 an hour
- Part-time
- Nursing
- RN License
- BLS Certification
Quick Apply
6d
Human Subject Research Coordinator II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Word processing
- Mid-level
- University
Clinical Trial Coordinator I/II FSP
Thermo Fisher Scientific —Rochester, NY
- $20 - $27 an hour
- Full-time
- Microsoft Word
- Computer literacy
- Mid-level
- Commuter assistance
- Paid parental leave
2d
Human Subject Research Coordinator I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- Word processing
- University
- Bachelor's degree
Outcomes Specialist I, CHeT
University of Rochester —Rochester, NY
- $23.27 - $32.60 an hour
- Full-time
- Hybrid work
- Microsoft Excel
- University
- Bachelor's degree
Public Health Project Spec II
University of Rochester —Rochester, NY
- $23.27 - $32.60 an hour
- Full-time
- Microsoft Excel
- Mid-level
- Office
6d
Sr. Clinical Trials Project Manager
University of Rochester —Rochester, NY
- $70,600 - $105,800 a year
- Full-time
- Hybrid work
- 5 years
- Master's degree
- University
7d
Human Subjects Research Coordinator II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Management
- Word processing
- Mid-level
Manager, Clinical Research
University of Rochester —Rochester, NY
- $70,600 - $105,800 a year
- Full-time
- Office
- Master's degree
- University
10d
Clin Research Reg Spt Spec II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Mid-level
- University
- Bachelor's degree
Clinical Research Assistant
ALLIANCE CLINICAL LLC —Rochester, NY
- $20 - $22 an hour
- Full-time
- Customer service
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply

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Clinical Research Coordinator

System One -
Rochester, NY

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Job Details

Contract
$26 - $30 an hour
7 days ago

Benefits

Health insurance
Dental insurance
401(k)
Vision insurance
Life insurance

Qualifications

Direct patient care
High school diploma or GED
Medical terminology

Full Job Description

Job Title: Clinical Research Coordinator
Location: Rochester, NY
Type: Contract
Compensation: $26.00 - $30.00/hr
Work Model: Onsite
Hours: 40.0

Leading Site located in Rochester, NY is hiring a Clinical Research Coordinator w/ 3+ years experience. If you want to be a part of this groundbreaking work, please apply!

Responsibilities

Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff.
Conduct screening visits to collect medical history & other information from study participants.
Assist with informed consent and enrollment of study participants in accordance with protocol requirements and ethical guidelines.
Coordinate and schedule study visits, procedures, and follow-up activities with study participants and clinical teams.
Collect, record, and maintain accurate clinical research data and source documentation in compliance with regulatory and institutional standards.
Communicate with study participants to provide education, answer questions, and support adherence to study requirements.
Monitor study progress and report adverse events, protocol deviations, and other study-related issues to the research team.
Adhere to site standard operating procedures (SOPs) and Good Clinical Practice (GCP) guidelines.
Draw, process, and ship laboratory specimens, including the handling of dangerous goods, in accordance with regulations (if qualified).
Scan, upload, file, and maintain organized study records and documentation.
Apply critical thinking skills to support efficient study operations and problem resolution.
Perform other duties as assigned.

Requirements

High school diploma or equivalent required; an associate’s degree or higher in a health-related field preferred.
Basic knowledge of clinical research strongly preferred.
Medical terminology & patient care experience required.
Strong organizational, time management, and attention-to-detail skills with the ability to manage multiple priorities.
Ability to communicate clearly and professionally with diverse populations.
Ability to work collaboratively in a fast-paced, team-oriented environment.
Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines strongly preferred.
Experience with participant screening and the informed consent process strongly preferred.
Proficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred.
Medical Assistant (MA) certification preferred.
Current CPR/BLS certification preferred.
Certification as a Clinical Research Coordinator (e.g., CCRC) or a willingness to obtain certification preferred.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M-
#LI-

Ref: #568-Clinical

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Refine Your Search

clinical research associate jobs in brighton ny

Clinical Research Coordinator

Clinical Research Data Spec I

Clinical Research Coordinator

Wilmot Cancer Center - Clinical Trials Office - Clinical Research Nurse - Registered Nurse 2, Outpatient

Clinical Research Spec II

Human Subject Research Spec II

Clinical Research Regulatory Specialist II

Human Subject Research Spec I

Research RN

Infusion Nurse

Human Subject Research Coordinator II

Clinical Trial Coordinator I/II FSP

Human Subject Research Coordinator I

Outcomes Specialist I, CHeT

Public Health Project Spec II

Sr. Clinical Trials Project Manager

Human Subjects Research Coordinator II

Manager, Clinical Research

Clin Research Reg Spt Spec II

Clinical Research Assistant

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