Clinical Research Associate Jobs in New York
Clinical Research Associate jobs in New York are among the most active in the country, concentrated in pharmaceutical development, academic medical centers, and contract research organizations, with openings from entry-level coordinators through senior and principal-level associates. Most hiring is in New York City, White Plains, and the Research Triangle corridor running through Westchester County, where established employers like Pfizer, Memorial Sloan Kettering Cancer Center, and IQVIA maintain significant clinical operations. Oncology, cardiovascular, and rare disease trials are the most in-demand specialties for clinical research associates across New York. Find a role that fits below and apply directly.
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Showing 5 of 68+ Clinical Research Associate jobs
INTRODUCTION
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
Within Danaher the work our diagnostic businesses do saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
We’re accelerating the development of cutting-edge diagnostics to solve some of the world’s most pressing health challenges. Across our diagnostics operating companies we are driving innovation through partnerships with top academic institutions and leading players in biopharma and translational research. We’re bringing the best minds together to accelerate innovation and unlock the full potential of the latest scientific advances. Together, we’re expanding access to precision diagnostics for millions of people worldwide – and we’re using our unmatched global scale and proven playbook to make it happen, from hospital labs to mobile clinics. By helping providers, patients, and families get faster, more precise diagnostic results, we’re improving treatment options and saving lives.
Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The Sr. Clinical Research Associate (Sr. CRA) is responsible for set-up, initiation, execution, monitoring and close-out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The Sr. CRA should be able to independently train and manage external clinical research sites.
This position reports to the Manager, Clinical Site Operations and is part of the Global Clinical Affairs organization. The position will be fully remote within the United States.
In this role, you will have the opportunity to:
- Oversee clinical study protocol execution at external sites, from start-up to close-out, ensuring timely data collection and compliance with FDA standards and Good Clinical Practice (GCP)
- Develop and maintain relationships with institutions, study investigators, internal stakeholders, and vendors to ensure successful trial execution, data integrity and adherence to project requirements
- Conduct independent study monitoring, including site coordination, investigational product accountability, and assessments of protocol deviations and/or adverse events, and drive clinical data quality which can include follow up on incomplete data entry and/or outstanding queries
- Manage IRB submissions and all study regulatory documentation to ensure Trial Master File is kept up to date and audit ready
- Contribute to study planning including budget and contract negotiation and timeline forecasts, site identification and qualifications, and process improvement initiatives within the Global Clinical Affairs organization; as well as prepare study documents, including creating clinical templates, such as informed consent forms, clinical monitoring plan, etc.
BASIC QUALIFICATIONS
The essential requirements of the job include:
- Bachelor’s degree with 5+ years clinical research experience OR Master’s degree with 3+ years clinical research experience OR Doctoral degree in field with 0-2 years clinical research experience
- Basic knowledge of regulatory requirements and Good Clinical Practice for in vitro diagnostic and medical device products
- Previous experience with managing clinical research sites and monitoring clinical study data
- Good technical background to understand and communicate current and new technologies
- Ability to work on multiple projects simultaneously
TRAVEL REQUIREMENTS
- Ability to travel 20-70%– including overnight(s), within the US. Travel may be up to 70% during project initiation periods
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- Retrospective/prospective biological sample procurement
- Experience with electronic Trial Master Files and Clinical Trial Management Systems
- Point-of-care research and knowledge of blood gas testing
COMPENSATION
The annual salary range OR the hourly range for this role is $103,000.00 - $130,000.00. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
INTRODUCTION
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
Within Danaher the work our diagnostic businesses do saves lives—and we’re all united by a shared commitment to innovate for tangible impact.
You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.
We’re accelerating the development of cutting-edge diagnostics to solve some of the world’s most pressing health challenges. Across our diagnostics operating companies we are driving innovation through partnerships with top academic institutions and leading players in biopharma and translational research. We’re bringing the best minds together to accelerate innovation and unlock the full potential of the latest scientific advances. Together, we’re expanding access to precision diagnostics for millions of people worldwide – and we’re using our unmatched global scale and proven playbook to make it happen, from hospital labs to mobile clinics. By helping providers, patients, and families get faster, more precise diagnostic results, we’re improving treatment options and saving lives.
Learn about the Danaher Business System which makes everything possible.
ROLE AND RESPONSIBILITIES
The Sr. Clinical Research Associate (Sr. CRA) is responsible for set-up, initiation, execution, monitoring and close-out of IVD and medical device clinical trials at external clinical research sites and/or laboratories. The Sr. CRA should be able to independently train and manage external clinical research sites.
This position reports to the Manager, Clinical Site Operations and is part of the Global Clinical Affairs organization. The position will be fully remote within the United States.
In this role, you will have the opportunity to:
- Oversee clinical study protocol execution at external sites, from start-up to close-out, ensuring timely data collection and compliance with FDA standards and Good Clinical Practice (GCP)
- Develop and maintain relationships with institutions, study investigators, internal stakeholders, and vendors to ensure successful trial execution, data integrity and adherence to project requirements
- Conduct independent study monitoring, including site coordination, investigational product accountability, and assessments of protocol deviations and/or adverse events, and drive clinical data quality which can include follow up on incomplete data entry and/or outstanding queries
- Manage IRB submissions and all study regulatory documentation to ensure Trial Master File is kept up to date and audit ready
- Contribute to study planning including budget and contract negotiation and timeline forecasts, site identification and qualifications, and process improvement initiatives within the Global Clinical Affairs organization; as well as prepare study documents, including creating clinical templates, such as informed consent forms, clinical monitoring plan, etc.
BASIC QUALIFICATIONS
The essential requirements of the job include:
- Bachelor’s degree with 5+ years clinical research experience OR Master’s degree with 3+ years clinical research experience OR Doctoral degree in field with 0-2 years clinical research experience
- Basic knowledge of regulatory requirements and Good Clinical Practice for in vitro diagnostic and medical device products
- Previous experience with managing clinical research sites and monitoring clinical study data
- Good technical background to understand and communicate current and new technologies
- Ability to work on multiple projects simultaneously
TRAVEL REQUIREMENTS
- Ability to travel 20-70%– including overnight(s), within the US. Travel may be up to 70% during project initiation periods
PREFERRED QUALIFICATIONS
It would be a plus if you also possess previous experience in:
- Retrospective/prospective biological sample procurement
- Experience with electronic Trial Master Files and Clinical Trial Management Systems
- Point-of-care research and knowledge of blood gas testing
COMPENSATION
The annual salary range OR the hourly range for this role is $103,000.00 - $130,000.00. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.
This job is also eligible for bonus/incentive pay.
We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.
Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
See All 68 Clinical Research Associate Jobs in New York
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Find JobsClinical Research Associate Jobs by City in New York
Where New York roles are concentrated, by current openings.
Clinical Research Associate Job Market in New York
A snapshot from current New York openings, updated as new roles post.
Who's Hiring
- Nicholas H. Noyes Memorial Hospital9
- NYU Langone Health8
- University at Buffalo8
- Columbia University5
- New York Society For Relief Of Ruptured & Crippled4
Top Industries Hiring
- Education33
- Healthcare & Medical Services21
- Science & Research7
- Consulting & Professional Services4
- Manufacturing3
What New York Employers Look For
The qualifications that appear most often in clinical research associate jobs across New York.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- ACRP or SOCRA certification such as CCRC or CCRP strongly preferred
- Two or more years of clinical trial monitoring or coordination experience
- Working knowledge of ICH-GCP guidelines and FDA regulatory requirements
- Proficiency with electronic data capture systems such as Medidata Rave or Veeva Vault
- Ability to travel regionally for on-site monitoring visits at New York and tri-state area sites
Clinical Research Associate Jobs in New York: Frequently Asked Questions
How do you become a clinical research associate in New York?
Most clinical research associates in New York enter the field with a bachelor's degree in a life science, nursing, or health-related discipline. New York does not require a state-issued license specific to clinical research, but earning a credential through ACRP or SOCRA, such as the CCRC or CCRP, is widely expected by New York employers. Starting as a clinical research coordinator at a hospital or academic medical center is the most common path before moving into a monitoring role.
Which companies hire clinical research associates in New York?
Employers hiring clinical research associates in New York right now include Nicholas H. Noyes Memorial Hospital, NYU Langone Health, and University at Buffalo, based on current listings on Migrate Mate as of June 2026. New York's dense concentration of academic medical centers, global pharma headquarters, and mid-size CROs means hiring activity is consistent across both the city and the surrounding suburban counties.
Which New York cities have the most clinical research associate jobs?
The cities with the most clinical research associate openings in New York are New York, Buffalo, and Elmwood Ave. New York City dominates because of its unmatched density of major medical centers, global pharmaceutical offices, and CRO hubs, while locations like White Plains and Tarrytown draw openings from the large biotech and pharma campuses anchored in Westchester County.
Are there remote clinical research associate jobs in New York?
Yes, but they are limited. About 12% of clinical research associate openings tied to New York are remote or hybrid as of June 2026, reflecting the fact that much of the role involves on-site monitoring visits at investigator sites. The parts of the work most suited to remote arrangements include protocol review, query resolution, and regulatory document management.
How can I get hired as a clinical research associate in New York with little or no experience?
The most realistic entry path is starting as a clinical research coordinator at one of New York City's large academic medical centers, such as NYU Langone, Mount Sinai, or NewYork-Presbyterian, which regularly hire new graduates into coordinator roles. From there, one to two years of site-facing experience makes candidates competitive for associate-level monitoring positions. Earning a CCRC credential early and building familiarity with an EDC platform significantly strengthens applications for candidates without direct monitoring history.
Where can I find and apply to clinical research associate jobs in New York?
You can find and apply to clinical research associate jobs in New York on Migrate Mate, which lists current New York openings updated regularly. Search the available roles, find ones that match your experience and target location, and apply directly to the positions that fit.
See All 68 Clinical Research Associate Jobs in New York
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