Research Associate
Chicago, IL ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
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Chicago, IL ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
Quick apply
Chicago, IL ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
New York, NY ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
New York, NY ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
San Diego, CA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
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San Diego, CA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
New York, NY ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
Quick apply
New York, NY ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
New York, NY ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
New York, NY ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
San Francisco, CA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
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San Francisco, CA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
Boston, MA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
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Boston, MA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
Denver, CO ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
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Denver, CO ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
Seattle, WA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
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Seattle, WA ยท On-site +1
You'll design and execute IRB protocols for strategically important clinical studies, manage ... This role is full-time and open to NYC-based or remote candidates. Our office is located in ...
... IRB, EC and regulatory authorities, as appropriate, translation of study related documentation ... remote EDC CRF and patient profiles review, query resolution, and assists data management and ...
... IRB, EC and regulatory authorities, as appropriate, translation of study related documentation ... remote EDC CRF and patient profiles review, query resolution, and assists data management and ...
Christiansburg, VA ยท Remote
$22.50 - $29.75/hr
... IRB processes * Strong organizational, documentation, and time management skills * Ability to ... Work Environment This position operates primarily in a remote setting; however, occasional travel ...
Christiansburg, VA ยท Remote
$22.50 - $29.75/hr
... IRB processes * Strong organizational, documentation, and time management skills * Ability to ... Work Environment This position operates primarily in a remote setting; however, occasional travel ...
OR ยท Remote
$95K - $115K/yr
Ensure strict adherence to study protocols, IRB/ethics board guidelines, and applicable federal ... Remote within the United States. This role requires 100% of work to be performed in a remote office ...
OR ยท Remote
$95K - $115K/yr
Ensure strict adherence to study protocols, IRB/ethics board guidelines, and applicable federal ... Remote within the United States. This role requires 100% of work to be performed in a remote office ...
... IRB, EC and regulatory authorities, as appropriate, translation of study related documentation ... remote EDC CRF and patient profiles review, query resolution, and assists data management and ...
... IRB, EC and regulatory authorities, as appropriate, translation of study related documentation ... remote EDC CRF and patient profiles review, query resolution, and assists data management and ...
... IRB, EC and regulatory authorities, as appropriate, translation of study related documentation ... remote EDC CRF and patient profiles review, query resolution, and assists data management and ...
... IRB, EC and regulatory authorities, as appropriate, translation of study related documentation ... remote EDC CRF and patient profiles review, query resolution, and assists data management and ...
Boston, MA ยท On-site +1
$55K - $61K/yr
... Research Manager and / or directly for the Clinical Trials Office to complete the regulatory ... This position's work location is fully remote with occasional time on-campus in Boston, MA. The ...
Boston, MA ยท On-site +1
$55K - $61K/yr
... Research Manager and / or directly for the Clinical Trials Office to complete the regulatory ... This position's work location is fully remote with occasional time on-campus in Boston, MA. The ...
Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Ability to manage multiple tasks, track milestones, and maintain detailed documentation.
Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Ability to manage multiple tasks, track milestones, and maintain detailed documentation.
... management, including site identification, feasibility, pre-study site evaluation, study start-up ... IRB/EC submissions of Coderas clinical studies at designated sites in accordance with study ...
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... management, including site identification, feasibility, pre-study site evaluation, study start-up ... IRB/EC submissions of Coderas clinical studies at designated sites in accordance with study ...
$26.25 - $35/hr
May be responsible for site IRB submissions (violations, deviations, severe adverse event reports ... Coordination and management of all clinical trials at the Satellite site(s), including ...
$26.25 - $35/hr
May be responsible for site IRB submissions (violations, deviations, severe adverse event reports ... Coordination and management of all clinical trials at the Satellite site(s), including ...
Boston, MA ยท On-site +1
$55K - $61K/yr
... Research Manager and / or directly for the Clinical Trials Office to complete the regulatory ... This position's work location is fully remote with occasional time on-campus in Boston. The ...
Boston, MA ยท On-site +1
$55K - $61K/yr
... Research Manager and / or directly for the Clinical Trials Office to complete the regulatory ... This position's work location is fully remote with occasional time on-campus in Boston. The ...
Job Summary Aptive Resources is seeking a management consultant with demonstrated research and ... IRB, NIH, VA). This is 100% remote position, with an option as either full-time or part-time. ...
Job Summary Aptive Resources is seeking a management consultant with demonstrated research and ... IRB, NIH, VA). This is 100% remote position, with an option as either full-time or part-time. ...
$58.5K - $62.2K
6% of jobs
$62.2K - $66K
7% of jobs
$66K - $69.7K
2% of jobs
$69.7K - $73.4K
6% of jobs
$74.5K is the 25th percentile. Wages below this are outliers.
$73.4K - $77.1K
9% of jobs
The median wage is $78.9K / yr.
$77.1K - $80.9K
40% of jobs
$81.5K is the 75th percentile. Wages above this are outliers.
$80.9K - $84.6K
20% of jobs
$84.6K - $88.3K
6% of jobs
$88.3K - $92K
1% of jobs
$92K - $95.8K
0% of jobs
$95.8K - $99.5K
1% of jobs
$58.5K
$78.6K
$99.5K
| Aspect | Remote Irb Manager | Remote Clinical Research Coordinator |
|---|---|---|
| Credentials | IRB certification, research administration experience | Clinical research training, sometimes certification |
| Work Environment | Office-based, administrative, compliance-focused | Remote, site coordination, participant interaction |
| Employer & Industry | Research institutions, pharma companies | Hospitals, research sites, CROs |
| Search & Comparison Intent | Understanding IRB oversight roles | Managing clinical trial logistics |
The Remote Irb Manager primarily oversees Institutional Review Board processes, ensuring compliance and ethical standards, often requiring IRB certification. The Remote Clinical Research Coordinator handles trial logistics, participant coordination, and data collection, with a focus on site operations. While both roles support clinical research, the Irb Manager emphasizes regulatory oversight, whereas the Coordinator focuses on trial execution.

Our mission is to improve people's health by making it easy to live a healthy lifestyle.
Nourish was founded to address a fundamental failure in the U.S. healthcare system: the rapid rise of chronic disease, which affects hundreds of millions of Americans and drives the majority of healthcare spending. Despite the clear role of nutrition and lifestyle in preventing, managing, and reversing these conditions, care has remained fragmented and inaccessible. Nourish has built the country's largest dietitian-led metabolic health clinic. We're an AI-native digital health system matching patients with 10,000+ Registered Dietitians, physicians, medications, lab testing, and AI agents to deliver insurance-covered care across all 50 states. Founded four years ago, we've completed millions of appointments, tripled year-over-year, and partnered with health plans covering 200M+ Americans across 250+ health systems.
In 2026 we raised a $100M Series C, bringing total funding to $215M. The round was led by Menlo Ventures, with participation from Thrive Capital, Index Ventures, J.P. Morgan Growth Equity Partners, Maverick Ventures, Y Combinator, BoxGroup, Atomico, Daybreak, and Operator Partners.
Learn more about our Series C here: Nourish Blog, Bloomberg, Fierce Healthcare, Digital Native, The Pulse Podcast.
Our clinical philosophyOur approach to care is grounded in meeting patients where they are and using evidence-based practices to drive long-term lifestyle, behavioral, and metabolic change. Our interdisciplinary care team provides personalized, in-depth, and expert-level care to patients from any and all backgrounds. We measure quality of outcomes against each patient's individual goals, coordinate seamlessly across care teams (RDs, NPs, physicians, outside providers), and continuously refine our approach through data, feedback and innovation. You can read more about our approach here.
As our first Research Associate, you will play a foundational role in building the operational infrastructure that makes Nourish's prospective clinical research possible โ owning the systems, processes, and study execution from protocol design through data collection, and helping translate research plans into published outputs and high-impact commercial evidence.
This is a highly hands-on role for a strong individual contributor who thrives in ambiguity and is excited to build. You'll design and execute IRB protocols for strategically important clinical studies, manage patient enrollment, draft white papers, conference abstracts, and contribute to peer-reviewed publications, and work closely with clinical operations, product, data, and commercial partners to ensure our research is both rigorous and operationally sound.
This person will report into our Head of Research and work closely with our clinical operations, product, data, and commercial teams. This role is full-time and open to NYC-based or remote candidates. Our office is located in Gramercy.
Key Responsibilities:This is not a job for everyone. We hold an extremely high bar because we believe talent density is our biggest competitive advantage. We're looking for people who actively choose hard, ambiguous problems, who run toward unglamorous work, give and receive candid feedback, and bring relentless resilience without the ego. Our work is important, but we are not self-important. We do this because we're solving one of the hardest problems in the world, and the problem matters. If that's you, we disproportionately reward it.
More Information:The Nourish Bar
Our Values
Why Nourish Exists
How We Work
Comp Philosophy
Benefits