Top 105 Clinical data Jobs in Rochester, Ny

Clinical Research Coordinator - Rochester NY
Kelly Services —Rochester, NY
- $28 - $30 an hour
- Full-time
- CPR Certification
- Microsoft Excel
- BLS Certification
- Paid holidays
- Disability insurance
Quick Apply
LPN Nursing Clinical Coordinator
Bryant and Stratton College —Rochester, NY
- $80,000 - $85,000 a year
- Nursing
- RN License
- Writing skills
- Health insurance
- Dental insurance
Quick Apply
11d
Manager, Clinical Research
University of Rochester —Rochester, NY
- $70,600 - $105,800 a year
- Full-time
- Office
- Master's degree
- University
Clinical Document Spec
University of Rochester —Rochester, NY
- $81,307 - $109,761 a year
- Full-time
- Remote
- Nursing
- Medicine
- Surgery
Clinical Admin II
University of Rochester —Brighton, NY
- $25.14 - $35.24 an hour
- Full-time
- Customer service
- Physical & Rehabilitation Medicine
- Mid-level
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
Asst Dir, Clinical Admin
University of Rochester —Rochester, NY
- $86,900 - $130,300 a year
- Full-time
- 5 years
- Clinic
- Bachelor's degree
Sr Data Analyst
University of Rochester —Rochester, NY
- $64,200 - $96,200 a year
- Full-time
- 5 years
- HIPAA
- Mid-level
Clinical Support Tech III
University of Rochester —Rochester, NY
- $20.75 - $28.01 an hour
- Weekends as needed
- Anatomy knowledge
- Mid-level
- Organizational skills
Assistant Director, Clinical Admin II
University of Rochester —Rochester, NY
- $97,400 - $146,000 a year
- Full-time
- 6 years
- Office
- Master's degree
Clin Research Data Spec I
University of Rochester —Rochester, NY
- $21.78 - $30.53 an hour
- Full-time
- University
- Bachelor's degree
- Organizational skills
Pediatric Clinical Safety Attendant
University of Rochester —Rochester, NY
- $19.15 - $25.85 an hour
- Part-time
- Nursing
- Mid-level
- Pediatrics
14d
Manger, Clinical Administration
University of Rochester —Rochester, NY
- $70,600 - $105,800 a year
- Full-time
- Psychiatry
- Mid-level
- 3 years
Manager, Clinical Research Data
University of Rochester —Rochester, NY
- $64,200 - $96,200 a year
- Full-time
- Master's degree
- University
- Bachelor's degree
Clinical Research Spec II
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Mid-level
- Clinic
- Bachelor's degree
Director, Clinical Admin
University of Rochester —Rochester, NY
- $109,000 - $163,600 a year
- Full-time
- 7 years
- Master's degree
- University
Assistant Director, Clinical Administration
University of Rochester —Rochester, NY
- $97,400 - $146,000 a year
- Full-time
- Writing skills
- Administrative experience
- Ob/Gyn
1d
Financial Spec I, Clinical Trials
University of Rochester —Rochester, NY
- $25.14 - $35.24 an hour
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Clinical Trials Proj Mgr II
University of Rochester —Rochester, NY
- $64,200 - $96,200 a year
- Full-time
- Surgery
- Customer service
- Word processing
Mgr, Clinical Trials Proj
University of Rochester —Rochester, NY
- $77,600 - $116,400 a year
- Full-time
- 6 years
- Surgery
- Office

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Clinical Research Coordinator - Rochester NY

Kelly Services -
Rochester, NY

Quick Apply

Job Details

Full-time
$28 - $30 an hour

Benefits

Paid holidays
Disability insurance
Health insurance
Dental insurance
Vision insurance
Retirement plan
Paid sick time

Qualifications

Direct patient care
High school diploma or GED
Medical terminology

Full Job Description

Kelly® Science & Clinical is seeking a Clinical Research Coordinator for a contract (temporary) position at a premier client of ours who is a mission-driven leader in advancing medical research, across various locations. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Salary/Pay Rate/Compensation: $28-30/hr depending on experience

Overview:
This company is a pioneering clinical research organization focused on advancing medical research by enrolling diverse populations in high-quality clinical trials. In this role, you’ll collaborate closely with Principal Investigators, research staff, and study participants to support and coordinate clinical trials. This is an opportunity to deepen your research skills, work in a supportive and collaborative environment, and help bring new therapies to patients and families while upholding the highest standards of integrity and excellence.

Schedule:
Normal working hours, onsite, 8-5EST or 9-6PMEST. This role is contracted until the end of 2026 with potential to be hired on permanent basis – NOT guaranteed

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 and 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

Qualifications:

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 and 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

Certificates, Licenses, and Registrations:

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

For more information or to be considered, send resumes to [email protected] or call 804-991-0745

As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.

Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.

Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.

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Refine Your Search

clinical data jobs in rochester, ny

Clinical Research Coordinator - Rochester NY

LPN Nursing Clinical Coordinator

Manager, Clinical Research

Clinical Document Spec

Clinical Admin II

Sr. Clinical Trials Project Manager

Asst Dir, Clinical Admin

Sr Data Analyst

Clinical Support Tech III

Assistant Director, Clinical Admin II

Clin Research Data Spec I

Pediatric Clinical Safety Attendant

Manger, Clinical Administration

Manager, Clinical Research Data

Clinical Research Spec II

Director, Clinical Admin

Assistant Director, Clinical Administration

Financial Spec I, Clinical Trials

Clinical Trials Proj Mgr II

Mgr, Clinical Trials Proj

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