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Senior Clinical Research Rater Jobs (NOW HIRING)

Rater

Dallas, TX · On-site

PCR seeks an experienced Research Rater who will be responsible for administering cognitive and clinical assessments. Raters are responsible for managing the psychometric aspects of clinical trials ...

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP ...

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP ...

Senior Clinical Research Coordinator

New York, NY · On-site

$26.50 - $35.25/hr

The Senior Clinical Research Coordinator (Sr. CRC) is an active participant in all related clinical ... The salary range or contractual rate listed does not include bonuses/incentive, differential pay or ...

Monday - Friday, 8:30 AM - 5:00 PM Pay: $32.00 - $43.00 per hour Job Summary We are seeking an experienced Senior Clinical Research Coordinator to support a busy clinical research team during a 15 ...

Senior Clinical Research Coordinator

Manhattan, NY · On-site

$26.75 - $35.50/hr

Position Summary We are seeking a Senior Clinical Research Coordinator to lead the day-to-day ... rating scales, cognitive batteries, safety assessments). * Serve as the primary site contact for ...

New

Select how often (in days) to receive an alert: Sr. Clinical Research Associate Date: Aug 14, 2026 Location: Waltham, MA, US Company: Paragonix Technologies, Inc. Remote Work: 1-2 days at home (site ...

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Senior Clinical Research Rater information

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$36K

$94.3K

$143.5K

How much do senior clinical research rater jobs pay per year?

As of Sep 13, 2026, the average yearly pay for senior clinical research rater in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What is the difference between Senior Clinical Research Rater vs Clinical Research Coordinator?

AspectSenior Clinical Research RaterClinical Research Coordinator
Required CredentialsTypically requires a background in healthcare, psychology, or related fields; certifications like CCRP are commonOften requires a degree in health sciences, nursing, or related fields; certifications like CCRP or CRC are beneficial
Work EnvironmentPrimarily conducts assessments, reviews data, and supports clinical trials remotely or in research settingsManages trial logistics, coordinates with sites, and oversees study activities in clinical settings
Employer & Industry UsageUsed by pharmaceutical companies, research organizations, and CROs for patient assessmentsEmployed by hospitals, research institutions, and CROs to manage trial operations

The main difference is that Senior Clinical Research Raters focus on evaluating patient data and assessments, often remotely, while Clinical Research Coordinators handle the overall management and coordination of clinical trials on-site. Both roles require healthcare or research backgrounds but serve different functions within the clinical research process.

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Senior Clinical Research Coordinator

Manhattan, NY • On-site

NYU Langone Health
Hospitals • 501 - 1,000 employees

$26.50 - $35.25/hr

Full-time

Re-posted 12 days ago


NYU Langone Health rating

8.4

Company rating: 8.4 out of 10

Based on 250 frontline employees who took The Breakroom Quiz


Job description

NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge.
For more information, go to med.nyu.edu, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, X and Instagram.

Position Summary:
We have an exciting opportunity to join our team as a Senior Clinical Research Coordinator.
The Senior Clinical Research Coordinator (Sr. CRC) is an active participant in all related clinical research studies from research planning and feasibility to completion of all study activities, including direct involvement in pre- and post-activation regulatory maintenance, case management of study participants, lab collection and processing, and data collection. The Sr. CRC works independently under the general supervision of research management within the CTSI Clinical Research Centers, in collaboration with the Principal Investigator and other study team members, to ensure GCP compliance in the conduct of the study, and adherence to the study protocol. The Sr. CRC provides mentorship to Associate Clinical Research Coordinators and Clinical Research Coordinators and participates in the Clinical Research Centers Orientation Program.

Job Responsibilities:

  1. Adhere to the IRB approved protocol and coordinate protocol related research procedures, study visits, and follow-up care ensuring the accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA, and all required obligations to patient/subject, Principal Investigator, Research Team and sponsor and other appropriate agencies. 

  1. Work with licensed clinicians and research managers to develop tracking forms for all active trials, maintain tracking forms throughout the life cycle of the protocol. 

  1. Act as primary point of contact for all assigned studies and patient visits. Coordinate with junior coordinators their schedules for the week.  

  1. Help to reconcile any clinical discrepancies in data with junior coordinators  

  1. Participates in pre-screening and recruitment activities to identify patients that may be eligible for a clinical trial. Trains clinical research coordinators on the process of pre-screening.  

  1. Write research notes in EPIC for specified visits as outlined by the protocol.  

  1. Schedule participants according to the approved protocol; coordinate with ancillary service providers to ensure patients remain adherent to the protocol. 

  1. Helps compile enrollment packet materials to be reviewed and signed by investigators.  


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