Clinical Research Associate Jobs in Buffalo, NY
Clinical Research Associate jobs in Buffalo, New York are in active demand, with employers like University at Buffalo and University at Buffalo - SUNY among those hiring. See the openings below and apply to the ones that match your experience.
Find JobsOverview
Open roles23
Top employerUniversity at Buffalo
Work type100% On-site
Companies hiring2
Showing 5 of 23+ Clinical Research Associate jobs
Clinical Research Associate I, Medicine
We won't show you this job again
Added 2w ago
University at Buffalo - SUNY
Clinical Research Associate I, Medicine
Buffalo, New York
Added 2w ago
Clinical Assistant/ Associate Professor
We won't show you this job again
Added 4mo ago
University at Buffalo
Clinical Assistant/ Associate Professor
Buffalo, New York
Added 4mo ago
Academic Scholar - Clinical Assistant, Associate, or Full Professor
We won't show you this job again
Added 4mo ago
University at Buffalo
Academic Scholar - Clinical Assistant, Associate, or Full Professor
Buffalo, New York
Added 4mo ago
Academic Scholar - Clinical Assistant, Associate, or Full Professor
We won't show you this job again
Added 4mo ago
University at Buffalo
Academic Scholar - Clinical Assistant, Associate, or Full Professor
Buffalo, New York
Added 4mo ago
Clinical Assistant/ Associate Professor
We won't show you this job again
Added 4mo ago
University at Buffalo
Clinical Assistant/ Associate Professor
Buffalo, New York
Added 4mo ago
Added 2w ago
Clinical Research Associate I, Medicine
University at Buffalo - SUNY·Buffalo, New York
Job functions:
$60k - $80k/yr
2+ yrs exp.
Certification
5,001-10,000 employees
Job Description
The Department of Medicine, Division of Behavioral Medicine is seeking a Clinical Research Associate I. In this role the Clinical Research Associate I will manage and coordinate a large-scale research study on temporomandibular disorders and chronic overlapping pain conditions.
The candidate will perform head, neck, and body examinations to obtain clinical data and to collect oral and biological samples as outlined in IRB-approved protocols. Additionally, the candidate must have experience with conducting research and working with RedCap databases and excel.
The candidate must be experienced with obtaining participant consent, developing standard operating protocols for research, and IRB submissions. Must also have completed CITI (Collaborative Institution Training Initiative) training certification in the ethics of research with human subjects.
The candidate will perform head, neck, and body examinations to obtain clinical data and to collect oral and biological samples as outlined in IRB-approved protocols. Additionally, the candidate must have experience with conducting research and working with RedCap databases and excel.
The candidate must be experienced with obtaining participant consent, developing standard operating protocols for research, and IRB submissions. Must also have completed CITI (Collaborative Institution Training Initiative) training certification in the ethics of research with human subjects.
The candidate must be willing to travel for training.
Recruitment and Participant Management
- Screen and recruit eligible study participants using IRB-approved study participant recruitment methods
- Schedule participant visits and maintain study timeline
- Obtain informed consent according to IRB and regulatory requirements
- Independently prioritize daily activities to ensure compliance with research requirements of all assigned study participants.
- Discuss study issues with the study investigators, serving as a liaison/advocate between the participant/family and the investigators.
Data Collection
- Provide education and information to study participants and families about clinical research participation and compliance.
- Conduct standardized examination of head, neck, and body. Review collected data
- Collect and manage biological samples (e.g., blood, saliva, stool)
- Track study supplies and research record and maintain accurate source documentation and case report forms
- Identify study implementation problems including unusual occurrences, safety concerns, issues with compliance with study requirements. Take an active role in resolving any implementation problems by participating in the development of study deviation reports and corrective action plans.
Administrative and Meetings
- Coordinate clinical research studies from startup through closeout
- Communicate with principal investigators, sponsors, monitors, and study participants and provide reports to the Principal Investigators in a timely manner.
- Prepare for monitoring visits, audits, and inspections
- Provide input into the development of amendments regarding study implementation.
IRB and compliance
- Ensure compliance with FDA, GCP, HIPAA, and institutional policies
- Devise, plan, and implement strategies and systems necessary to ensure adherence to and compliance with the assigned clinical research studies.
Learn more:
- Our benefits, where we prioritize your well-being and success to enhance every aspect of your life.
- Being a part of the University at Buffalo community.
As an Equal Opportunity / Affirmative Action employer, the Research Foundation will not discriminate in its employment practices due to an applicant’s race, color, religion, sex, sexual orientation, gender identity, national origin and veteran or disability status.
Minimum Qualifications
- Bachelor’s degree plus 2 years of experience or equivalent combination of education and experience.
- Knowledge of medical terminology; good computer skills; good communication and organizational skills.
Preferred Qualifications
- Bachelor’s degree in Dental Hygiene
- Certifications for CPR/BLS, phlebotomy, GCP, IRB
- Experience in clinical research or healthcare coordination
- Strong organizational, communication, interpersonal, and documentation skills
- Possession of health career skills including principles and techniques, medical terminology, drugs, patient education and counseling.
- Computer skills (Microsoft Word, Excel, PowerPoint) and skills related to data collection (e.g., REDCap) and management.
- Ability to prioritize, multi-task and organize independently in a research environment and problem solve with minimal supervision.
- Strong attention to detail, ability to function autonomously in a collaborative multidisciplinary team and willingness to learn
Physical Demands
Driving Requirements
This position does not drive a university owned vehicle
Salary Range
$60,000 - $80,000
Additional Salary Information
The salary range reflects our good faith and reasonable estimate of the possible compensation at the time of posting, the role and associated responsibilities, and the experience, education, and training of the selected candidate.
Work Hours
37.5 hours per week
Campus
Erie County Medical Center
Posting Alerts
Special Instructions Summary
Is a background check required for this posting?
No
Background Check Notification
University at Buffalo - SUNY
Clinical Research Associate I, Medicine
Buffalo, New York
Added 2w ago5,001-10,000 employees
Job functions:
$60k - $80k/yr
2+ yrs exp.
Certification
Job Description
The Department of Medicine, Division of Behavioral Medicine is seeking a Clinical Research Associate I. In this role the Clinical Research Associate I will manage and coordinate a large-scale research study on temporomandibular disorders and chronic overlapping pain conditions.
The candidate will perform head, neck, and body examinations to obtain clinical data and to collect oral and biological samples as outlined in IRB-approved protocols. Additionally, the candidate must have experience with conducting research and working with RedCap databases and excel.
The candidate must be experienced with obtaining participant consent, developing standard operating protocols for research, and IRB submissions. Must also have completed CITI (Collaborative Institution Training Initiative) training certification in the ethics of research with human subjects.
The candidate will perform head, neck, and body examinations to obtain clinical data and to collect oral and biological samples as outlined in IRB-approved protocols. Additionally, the candidate must have experience with conducting research and working with RedCap databases and excel.
The candidate must be experienced with obtaining participant consent, developing standard operating protocols for research, and IRB submissions. Must also have completed CITI (Collaborative Institution Training Initiative) training certification in the ethics of research with human subjects.
The candidate must be willing to travel for training.
Recruitment and Participant Management
- Screen and recruit eligible study participants using IRB-approved study participant recruitment methods
- Schedule participant visits and maintain study timeline
- Obtain informed consent according to IRB and regulatory requirements
- Independently prioritize daily activities to ensure compliance with research requirements of all assigned study participants.
- Discuss study issues with the study investigators, serving as a liaison/advocate between the participant/family and the investigators.
Data Collection
- Provide education and information to study participants and families about clinical research participation and compliance.
- Conduct standardized examination of head, neck, and body. Review collected data
- Collect and manage biological samples (e.g., blood, saliva, stool)
- Track study supplies and research record and maintain accurate source documentation and case report forms
- Identify study implementation problems including unusual occurrences, safety concerns, issues with compliance with study requirements. Take an active role in resolving any implementation problems by participating in the development of study deviation reports and corrective action plans.
Administrative and Meetings
- Coordinate clinical research studies from startup through closeout
- Communicate with principal investigators, sponsors, monitors, and study participants and provide reports to the Principal Investigators in a timely manner.
- Prepare for monitoring visits, audits, and inspections
- Provide input into the development of amendments regarding study implementation.
IRB and compliance
- Ensure compliance with FDA, GCP, HIPAA, and institutional policies
- Devise, plan, and implement strategies and systems necessary to ensure adherence to and compliance with the assigned clinical research studies.
Learn more:
- Our benefits, where we prioritize your well-being and success to enhance every aspect of your life.
- Being a part of the University at Buffalo community.
As an Equal Opportunity / Affirmative Action employer, the Research Foundation will not discriminate in its employment practices due to an applicant’s race, color, religion, sex, sexual orientation, gender identity, national origin and veteran or disability status.
Minimum Qualifications
- Bachelor’s degree plus 2 years of experience or equivalent combination of education and experience.
- Knowledge of medical terminology; good computer skills; good communication and organizational skills.
Preferred Qualifications
- Bachelor’s degree in Dental Hygiene
- Certifications for CPR/BLS, phlebotomy, GCP, IRB
- Experience in clinical research or healthcare coordination
- Strong organizational, communication, interpersonal, and documentation skills
- Possession of health career skills including principles and techniques, medical terminology, drugs, patient education and counseling.
- Computer skills (Microsoft Word, Excel, PowerPoint) and skills related to data collection (e.g., REDCap) and management.
- Ability to prioritize, multi-task and organize independently in a research environment and problem solve with minimal supervision.
- Strong attention to detail, ability to function autonomously in a collaborative multidisciplinary team and willingness to learn
Physical Demands
Driving Requirements
This position does not drive a university owned vehicle
Salary Range
$60,000 - $80,000
Additional Salary Information
The salary range reflects our good faith and reasonable estimate of the possible compensation at the time of posting, the role and associated responsibilities, and the experience, education, and training of the selected candidate.
Work Hours
37.5 hours per week
Campus
Erie County Medical Center
Posting Alerts
Special Instructions Summary
Is a background check required for this posting?
No
Background Check Notification
See All 23 Clinical Research Associate Jobs in Buffalo
Find roles in Buffalo that match your experience and apply in just a few clicks.
Find JobsClinical Research Associate Job Market in Buffalo
Who's Hiring
- University at Buffalo22
- University at Buffalo - SUNY1
Top Industries Hiring
- Education22
- Healthcare & Medical Services1
Clinical Research Associate Jobs in Buffalo: Frequently Asked Questions
How many clinical research associate jobs are there in Buffalo?
There are 23+ clinical research associate openings in Buffalo, New York on Migrate Mate as of June 2026. New positions post regularly as Buffalo employers hire.
Which companies hire clinical research associates in Buffalo?
Buffalo clinical research associate roles are posted by University at Buffalo and University at Buffalo - SUNY and others right now, based on current listings on Migrate Mate as of June 2026.
Are there remote clinical research associate jobs in Buffalo?
Yes. About 0% of clinical research associate openings tied to Buffalo are remote or hybrid as of June 2026. The rest are on-site roles based in and around Buffalo.
Which industries hire the most clinical research associates in Buffalo?
Most clinical research associate openings in Buffalo sit in Education and Healthcare & Medical Services, per current listings on Migrate Mate as of June 2026.
Related Jobs in New York
See All 23 Clinical Research Associate Jobs in Buffalo
Find roles in Buffalo that match your experience and apply in just a few clicks.
Find Jobs