Top 622 Fda regulatory Jobs in New York, Ny

Clinical Research Coordinator
Burke Rehabilitation Hospital —White Plains, NY
- $70,000 a year
- Full-time
- Hospital
- HIPAA
- Inpatient
Regulatory and Compliance Analyst
APOLLO PHARMA INC —New York, NY
- $45 an hour
- Part-time
- HIPAA
- Bachelor's degree
- In-person
Quick Apply
Regulatory Associate
CEDENT —New York, NY
- Contract
- Microsoft Excel
- Mid-level
- Project management
Regulatory and Compliance Analyst
BROOKDALE PHARMA INC —Brooklyn, NY
- $45 an hour
- Part-time
- HIPAA
- Office
- Bachelor's degree
- Paid time off
Quick Apply
13d
Project Manager
Columbia University —New York, NY
- $92,625 - $97,375 a year
- Full-time
- Computer literacy
- Mid-level
- Bachelor's degree
Research Coordinator
Weill Cornell Medicine —New York, NY
- $68,200 - $77,500 a year
- Monday to Friday
- Mid-level
- Office
- Bachelor's degree
1d
Regulatory Affairs/Quality Affairs Specialist
Elliquence —Baldwin, NY
- $75,000 - $87,000 a year
- Full-time
- Master's degree
- Bachelor's degree
- Continuous improvement
Manager/Senior Manager, Global Regulatory Affairs
Menarini Group —New York, NY
- $135,000 - $180,000 a year
- Bachelor of Science
- Office
- Bachelor's degree
- Health savings account
- AD&D insurance
Compliance Data Scientist
Rendr —New York, NY
- $110,000 - $135,000 a year
- Computer Science
- 5 years
- HIPAA
- Commuter assistance
- Health savings account
Regulatory Affairs Specialist
Elliquence —Baldwin, NY
- $75,000 - $85,000 a year
- Full-time
- Mid-level
- Master's degree
- Bachelor's degree
Life Sciences Counsel
Anthropic —New York, NY
- $335,000 - $385,000 a year
- Hybrid work
- Office
- Bachelor's degree
- Experience equivalent to degree accepted
- Parental leave
- Flexible schedule
6d
Flex Shopper - Part Time
Whole Foods Market —New York, NY
- $18.00 - $25.40 an hour
- 8 hour shift
- Hospitality
- 18 years or older
- English
- Store discount
- Paid time off
Microbiology Ops Specialist
Spore.Bio —New York, NY
- $80,000 - $110,000 a year
- Hybrid work
- Mid-level
- Analysis skills
- Travel
- Dental insurance
- Vision insurance
Regulatory Affairs / Food Labeling
Nassau Candy —Hicksville, NY
- $70,000 - $90,000 a year
- Oracle
- Mid-level
- 3 years
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator
Columbia University —New York, NY
- $64,350 - $65,000 a year
- Full-time
- Hybrid work
- Patient monitoring
- Mid-level
- Bachelor's degree
- Retirement plan
Administrator II - IRB
Nathan S. Kline Institute —Orangeburg, NY
- $78,285 - $94,392 a year
- Full-time
- Bachelor of Science
- Mid-level
- Analysis skills
Quick Apply
Regulatory Affairs Specialist
Sunrise Pharma —Rahway, NJ
- Monday to Friday
- 5 years
- Master's degree
- Senior level
Clinical Research Coord I
Columbia University —New York, NY
- $68,000 a year
- Full-time
- Microsoft Word
- Writing skills
- English
6d
Research Associate I
Montefiore Einstein —Bronx, NY
- $53,040 - $66,300 a year
- Full-time
- Hospital
- Mid-level
- Microsoft Office
Assistant General Counsel, Regulatory Compliance
Danaher Diagnostics —New York, NY
- $250,000 - $275,000 a year
- Full-time
- Remote
- 8 years
- Analysis skills
- Travel
- Health insurance
- Dental insurance

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Clinical Research Coordinator

Burke Rehabilitation Hospital -
White Plains, NY

Apply Now

Job Details

Full-time
$70,000 a year

Qualifications

Bachelor's degree

Full Job Description

City/State:

White Plains, New York

Department:

Executive Medical Administration

Work Shift:

Day

Work Days:

MON-FRI

Scheduled Hours:

8 AM-4 PM

Scheduled Daily Hours:

7 HOURS

Pay Rate/Range:

$70,000

Sign-On Bonus:

n/a

Burke Rehabilitation is enthusiastically seeking a Clinical Research Coordinator (CRC) who will join the Research Team to help further advance the institution’s clinical and academic research portfolio. Reporting to the Senior Manager of Clinical Research Compliance, this position supports the Department of Clinical Research and Innovation at BRH by coordinating and assisting with clinical trials, investigator-initiated studies, and academic research activities across inpatient and outpatient rehabilitation settings. The CRC plays a key role in ensuring regulatory compliance, high-quality data collection, and operational execution of research aligned with BRH’s mission to advance rehabilitation outcomes through innovation.

Major Accountabilities and Responsibilities

Research Operations & Coordination

Coordinate day-to-day activities for clinical and academic research studies, including industry-sponsored trials, federally funded studies, and investigator-initiated projects.
Perform study feasibility support, patient screening, recruitment, enrollment, and informed consent in accordance with protocol and institutional requirements.
Knowledgeable about study workflows across inpatient and outpatient settings, including use of Epic (research workflows/orders), eRehab, and other data systems.
Assist in biospecimen collection, processing, storage, and shipment per protocol requirements.

Regulatory & Compliance

Support regulatory processes including IRB submissions, modifications, continuing reviews, and study closeout in coordination with BRH leadership and Einstein/Montefiore IRB (iRIS) or external IRBs.
Ensure adherence to Good Clinical Practice (GCP), HIPAA, FDA regulations, and AAHRPP standards, as well as BRH institutional policies and pre-IRB review processes.
Maintain regulatory binders, study documentation, and audit readiness.

Data Management & Quality

Perform and oversee data collection, entry, validation, and query resolution using study databases (e.g., Qualtrics, sponsor EDC systems).
Ensure accurate and timely source documentation and data reporting to sponsors and internal stakeholders.
Track study metrics including enrollment, compliance, and outcomes.

Academic & Scholarly Support

Assist investigators, residents, and staff with academic research activities, including:
Literature reviews and evidence synthesis
Abstracts, manuscripts, and conference submissions
Poster and oral presentations
Support quality improvement (QI) and program evaluation initiatives aligned with BRH clinical priorities.

Collaboration & Communication

Serve as a liaison between Principal Investigators, clinicians, research leadership, and external partners (e.g., sponsors, CROs, IRBs).
Communicate study requirements and workflows to interdisciplinary clinical teams, ensuring integration into patient care.
Provide education and support to patients and families, explaining study participation, procedures, and expectations in a patient-centered manner.

Financial & Operational Support

Assist with study start-up activities, including coordination of study materials and tracking timelines.
Support research finance workflows including study tracking, visit documentation, and coordination with billing/compliance teams.

Competencies and Work Experience

Research experience in a hospital or academic medical setting (rehabilitation or neurology) preferred.
Strong understanding of clinical trial coordination, regulatory processes, and IRB submissions.
Excellent organizational, communication, and interpersonal skills; ability to work independently and coordinate multiple studies simultaneously.
Commitment to maintaining confidentiality and ethical standards in clinical research
Ability to collaborate effectively with multidisciplinary clinical and research teams.

Education Requirements

Bachelor’s degree in a scientific, health-related, or relevant field required.
Clinical research certification (e.g., CCRC, CCRP, CRA, or equivalent) preferred or expected within a defined timeframe.

The Burke Rehabilitation Hospital is an equal employment opportunity employer. The Burke Rehabilitation Hospital will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law.

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Refine Your Search

fda regulatory jobs in new york, ny

Clinical Research Coordinator

Regulatory and Compliance Analyst

Regulatory Associate

Regulatory and Compliance Analyst

Project Manager

Research Coordinator

Regulatory Affairs/Quality Affairs Specialist

Manager/Senior Manager, Global Regulatory Affairs

Compliance Data Scientist

Regulatory Affairs Specialist

Life Sciences Counsel

Flex Shopper - Part Time

Microbiology Ops Specialist

Regulatory Affairs / Food Labeling

Clinical Research Coordinator

Administrator II - IRB

Regulatory Affairs Specialist

Clinical Research Coord I

Research Associate I

Assistant General Counsel, Regulatory Compliance

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