clinical research in new york

• Weill Cornell Medicine

A Weill Cornell Medicine and New York-Presbyterian collaboration to advance clinical research

Clinical Trials Day 2022

Clinical trials are changing medicine at Weill Cornell Medicine and NewYork-Presbyterian Hospital. 

Search by Location

We offer clinical trials across New York City and Westchester.

Questions to ask your healthcare team

Thinking of enrolling in a clinical trial? Here's what to ask. 

What is a clinical trial?

Clinical trials are intended to advance medical knowledge. 

Clinical Trials

If you are interested in joining a study or want to learn more about our research, please browse our studies by clicking the photo above.

Getting Started in Research

Learn more about types of research and the steps involved in initiating a clinical trial at WCM/NYP.

Researcher's Toolbox

Tools and templates for use throughout the clinical trial process

Partner with the JCTO

Information about collaborating with our investigators and institution

News from around the WCM/NYP research community

Patient Outreach Center:

IMA Clinical Research Manhattan

About this site.

This site is situated in the heart of Manhattan, just two blocks away from Times Square, providing easy access to patients using mass transit from other boroughs. This is a multi-therapeutic specialty facility with multiple principal investigators having conducted over 200 clinical trials in therapeutic areas such as cardiology, endocrinology, gastroenterology, immunology, infectious disease, nephrology, metabolic disorders, pain, and vaccines.

33 West 46th Street, Suite 4W New York, NY 10036

646-722-6214

Hours of Operation

Monday-Friday: 7:30-3:30 Saturday-Sunday: closed

Current Studies

• ASCVD (Cardiovascular Disease)
• Flu Vaccine
• Healthy Volunteers
• Hypertension
• NASH (Non-alcoholic Fatty Liver Disease)
• Osteoarthritis

More Study Opportunities

Explore additional study opportunities at this site beyond current enrollments:

• Abdominal Pain
• Acid Reflux in Gastroesophageal
• Acute Uncomplicated Influenza
• Alzheimer’s Disease Prevention
• Cardiovascular Event Prevention/outcomes
• Carpal Tunnel Syndrome
• Chronic Pain (non-malignant)
• Clostridium Difficile Infection
• Constipation
• Crohn’s Disease
• Eosinophilic Esophagitis
• Familial hypercholesterolemia
• Flash Glucose Monitoring System
• Gastrointestinal System Disorder
• Gastroparesis
• Headaches and Migraines
• Heart Failure
• Hypercholesterolemia
• Hyperlipidemia
• Hypertriglyceridemia
• Hypoglycemia
• Irritable Bowel Syndrome (IBS)
• Liver Disorders
• Other Heart Disorders
• Smoking Cessation
• Thyroid Disorders
• Triglycerides
• Vaccine (CMV, COVID, Dengue, Lyme, Pneumonia, RSV)

While these indications aren’t actively recruiting now, your interest could shape future studies. Click “Register” to express your interest and be part of upcoming research endeavors.

IMA Clinical Research Phoenix

IMA Clinical Research St. Petersburg

IMA Clinical Research Chicago

Explore Resources & Events

Atherosclerosis treatment through the years, the complexity of obesity, vaccines on the rise, any questions, privacy overview.

About Integrated Medical Professionals (IMP) Research

Integrated medical professionals (imp) research is a multi-specialty medical clinical trial research site located in midtown manhattan. assisting some of the world's finest pharmaceutical companies uncover new treatments, we help patients better manage their healthcare. conducting clinical trials and research studies for a most medical specialties; including urology, dermatology, gastroenterology, endocrinology/diabetes, sexual dysfunction and more. we urge you to explore our website to learn about our current research study opportunities and our impressive medical staff responsible for overseeing them..

UTI Research

Low Testosterone

Motion Sickness

OAB & BPH

Bladder Cancer

Click here for a list of our current studies.

Participate in a Trial

• Diabetic Neuropathy
• Fibromyalgia
• Other Studies

  The Premier Clinical Research Facility

Fieve Clinical Research, Inc. (FCR) is a private research center located at 587 Fifth Avenue -- one of the busiest and most central locations of New York City, next to Rockefeller Center. FCR was started in 2010 by Vanessa Fieve, JD, CCRC, who has over 20 years of Clinical Research experience and more than 10 years specifically managing Fieve Clinical Services, Inc., a site started by her late father Ronald R. Fieve, MD in 1983. The clinic has earned a reputation as one of the most reliable study centers in the United States for conducting research trials on new compounds in Phases II-IV of their development.

FCR has worked with many major pharmaceutical companies, both domestic and foreign, as well as a number of well-known Contract Research Organizations (CROs). The therapeutic areas we specialize in include Psychiatry, Internal Medicine, Neurology/Pain Management, Endocrinology and Immunology.

Our Research Team

Our principal investigators & study staff have worked with many major pharmaceutical companies.

Extensive Experience

Over 18 years experience in sponsored clinical trials in depression and other areas.

Convenient Location

Fieve Clinical Research facility is easily accessible to patients, located near Rockefeller Center.

Request Information

We’re happy to send you additional information on trial participation, sponsorship, or our facility.

(504) 934-8424

(985) 219-6501

(504) 934-8092

(985) 302-0470

(646) 386-7574

(407) 636-4031

(732) 724-2500

(407) 680-0534

Tandem Clinical Research Is a Dedicated Phase I-IV Clinical Trials Network

We specialize in the performance of clinical trials for pharmaceutical, biotech, and medical device companies. All medical service is provided free of charge by board-certified physicians. Click an image below to learn more.

How Does It Work?

What to Expect?

Benefits of Participating

How do clinical trials work.

Clinical trials are a crucial part of clinical research that test new medical treatments, drugs, or interventions on human participants to determine their safety and effectiveness. Here’s how they work:

• Study Design: Before a clinical trial begins, researchers carefully plan and design the study. They define the objectives, eligibility criteria for participants, and the treatment plan. This design ensures that the trial produces reliable and meaningful results.
• Phases of Clinical Trials: Clinical trials are typically conducted in multiple phases: a. Phase 1: These trials involve a small number of healthy volunteers to assess the treatment’s safety, dosage, and potential side effects. b. Phase 2: In this stage, the treatment is given to a larger group of patients who have the specific condition the treatment aims to address. Researchers monitor its effectiveness and further evaluate its safety. c. Phase 3: The treatment is tested on an even larger group of patients to compare its effectiveness against existing standard treatments or placebos. This phase provides more comprehensive data on safety and efficacy. d. Phase 4: After the treatment receives regulatory approval, Phase 4 trials are conducted to monitor its long-term safety and effectiveness in a broader population.
• Randomization: Participants are randomly assigned to different groups. For example, in a Phase 3 trial, some participants might receive the new treatment while others receive the standard treatment or a placebo. This randomization helps minimize bias and ensures fair comparisons.
• Blinding (Masking): Blinding means that participants and/or researchers may not know which treatment each participant is receiving. This prevents bias and helps obtain more objective results. Trials can be single-blind (participants don’t know), double-blind (neither participants nor researchers know), or open-label (both know).
• Informed Consent: Before joining a clinical trial, participants must receive detailed information about the study, including potential risks and benefits. They give their informed consent to participate voluntarily.
• Monitoring and Data Collection: Throughout the trial, researchers closely monitor participants’ health and collect data on their responses to the treatment. This includes regular check-ups, tests, and questionnaires.
• Analysis and Results: After the trial is completed, researchers analyze the data to determine the treatment’s effectiveness and safety. The results are usually published in scientific journals, contributing to medical knowledge.
• Regulatory Approval: If the treatment proves to be safe and effective, it may be submitted for regulatory approval from health authorities before becoming available to the public.
• Ethical Considerations: Clinical trials adhere to strict ethical guidelines to protect the rights and well-being of participants. Institutional Review Boards (IRBs) or Ethics Committees review and approve the study protocols to ensure participants’ safety and privacy.

By following these steps, clinical trials provide critical evidence for deciding which treatments are safe and beneficial, advancing medical knowledge, and improving patient care. Tandem Clinical Research is proud to be part of this important process.

What Can a Study Participant Expect?

As a participant in a clinical trial, you can expect a structured and carefully monitored experience aimed at evaluating the safety and effectiveness of a new medical treatment, drug, or intervention. Here’s what you can typically expect:

• Informed Consent: Before joining the trial, you will be given detailed information about the study, including its purpose, procedures, potential risks, benefits, and your rights as a participant. This is known as the informed consent process. Take your time to review the information, ask questions, and ensure you understand everything before giving your consent.
• Screening Process: You’ll undergo a screening process to determine if you meet the specific eligibility criteria for the trial. These criteria may include age, gender, medical condition, medical history, and current health status.
• Randomization and Assignment: If you meet the criteria and agree to participate, you may be randomly assigned to one of the treatment groups. This randomization ensures unbiased and fair comparisons between different treatments.
• Study Procedures: Depending on the phase of the trial, you may receive the new treatment being tested, a standard treatment, or a placebo (if applicable). The trial’s procedures, including dosages, frequency of treatments, and follow-up visits, will be clearly explained to you.
• Monitoring and Follow-up: Throughout the trial, you will be closely monitored by healthcare professionals. They will conduct regular check-ups, tests, and assessments to track your progress and the treatment’s effects.
• Adherence to Protocol: It’s essential to follow the trial’s protocol and any instructions given by the research team. This consistency ensures the trial’s accuracy and reliability.
• Possible Risks and Side Effects: Be aware of potential risks and side effects associated with the treatment. The research team will inform you about these during the informed consent process and will be available to address any concerns you may have during the trial.
• Continued Medical Care: Even though you’re participating in a trial, you will continue to receive medical care for your condition. The research team will coordinate with your primary healthcare provider to ensure your well-being.
• Privacy and Confidentiality: Your privacy will be protected, and your personal information will be kept confidential in accordance with ethical guidelines and privacy laws.
• Open Communication: Feel free to communicate openly with the research team about any changes in your health, questions, or concerns. They are there to support and guide you throughout the trial.
• Voluntary Participation: Remember that participating in a clinical trial is entirely voluntary. You have the right to withdraw from the trial at any time without any penalty or impact on your regular medical care.

Clinical trials play a crucial role in advancing medical knowledge and improving patient care, and your participation contributes to these important efforts. Tandem Clinical Research takes great care to ensure your safety and well-being are the top priorities throughout the entire trial process.

Benefits of Participating In A Clinical Trial

Participating in a clinical research study offers several benefits, not just for the individual participant but also for the advancement of medical knowledge and the improvement of healthcare as a whole. Some of the key benefits include:

• Access to New Treatments: Participants in clinical research studies often get access to cutting-edge treatments, drugs, or interventions that may not be available through regular medical channels. This provides an opportunity to explore potential benefits not yet widely accessible.
• Advancing Medical Knowledge: By participating in research, individuals contribute directly to the expansion of medical knowledge. The data collected from the study helps researchers and healthcare professionals better understand diseases, their causes, and potential treatments.
• Improved Personal Healthcare: The careful monitoring and follow-up involved in clinical research can lead to a deeper understanding of the participant’s health condition. This can result in better disease management and personalized healthcare recommendations.
• Close Medical Supervision: Participants receive close medical supervision and attention from qualified healthcare professionals throughout the study. This frequent monitoring can identify health issues or concerns early on and allow for prompt intervention.
• Helping Others: Clinical research studies are essential for finding new and better treatments for various medical conditions. By participating, individuals directly contribute to the development of therapies that may benefit future patients and improve overall public health.
• Access to Expert Care: Clinical trials are often conducted at major medical centers and research institutions, where participants can receive care from expert healthcare providers and researchers.
• Cost Savings: In some cases, participating in a clinical trial may reduce the cost of treatment, as the study sponsor may cover some or all of the expenses related to the trial.
• Support and Education: Participants are provided with information and education about their condition and the treatment being studied. This empowers them to make informed decisions about their healthcare.
• Opportunity for Rare Conditions: For individuals with rare or challenging medical conditions, clinical trials may offer one of the few opportunities to explore potential treatments tailored to their specific needs.
• Contribution to Society: Being part of a clinical research study is a way of giving back to society and making a significant impact on the future of medicine and healthcare.

It’s important to note that while there are many benefits, clinical research also involves potential risks, and not every study may be suitable for every individual. Before deciding to participate in a clinical trial, it is crucial to carefully review the study information, ask questions, and discuss with the research team and your healthcare provider to make an informed choice.

Clinical trials are a crucial part of clinical research that test new medical treatments, drugs, or interventions on human participants to determine their safety and effectiveness. Here’s how they work: 1. Study Design: Before a clinical trial begins, researchers carefully plan and design the study. They define the objectives, eligibility criteria for participants, and the treatment plan. This design ensures that the trial produces reliable and meaningful results. 2. Phases of Clinical Trials: Clinical trials are typically conducted in multiple phases: a. Phase 1: These trials involve a small number of healthy volunteers to assess the treatment’s safety, dosage, and potential side effects. b. Phase 2: In this stage, the treatment is given to a larger group of patients who have the specific condition the treatment aims to address. Researchers monitor its effectiveness and further evaluate its safety. c. Phase 3: The treatment is tested on an even larger group of patients to compare its effectiveness against existing standard treatments or placebos. This phase provides more comprehensive data on safety and efficacy. d. Phase 4: After the treatment receives regulatory approval, Phase 4 trials are conducted to monitor its long-term safety and effectiveness in a broader population. 3. Randomization: Participants are randomly assigned to different groups. For example, in a Phase 3 trial, some participants might receive the new treatment while others receive the standard treatment or a placebo. This randomization helps minimize bias and ensures fair comparisons. 4. Blinding (Masking): Blinding means that participants and/or researchers may not know which treatment each participant is receiving. This prevents bias and helps obtain more objective results. Trials can be single-blind (participants don’t know), double-blind (neither participants nor researchers know), or open-label (both know). 5. Informed Consent: Before joining a clinical trial, participants must receive detailed information about the study, including potential risks and benefits. They give their informed consent to participate voluntarily. 6. Monitoring and Data Collection: Throughout the trial, researchers closely monitor participants’ health and collect data on their responses to the treatment. This includes regular check-ups, tests, and questionnaires. 7. Analysis and Results: After the trial is completed, researchers analyze the data to determine the treatment’s effectiveness and safety. The results are usually published in scientific journals, contributing to medical knowledge. 8. Regulatory Approval: If the treatment proves to be safe and effective, it may be submitted for regulatory approval from health authorities before becoming available to the public. 9. Ethical Considerations: Clinical trials adhere to strict ethical guidelines to protect the rights and well-being of participants. Institutional Review Boards (IRBs) or Ethics Committees review and approve the study protocols to ensure participants’ safety and privacy. By following these steps, clinical trials provide critical evidence for deciding which treatments are safe and beneficial, advancing medical knowledge, and improving patient care. Tandem Clinical Research is proud to be part of this important process.

As a participant in a clinical trial, you can expect a structured and carefully monitored experience aimed at evaluating the safety and effectiveness of a new medical treatment, drug, or intervention. Here’s what you can typically expect: 1. Informed Consent: Before joining the trial, you will be given detailed information about the study, including its purpose, procedures, potential risks, benefits, and your rights as a participant. This is known as the informed consent process. Take your time to review the information, ask questions, and ensure you understand everything before giving your consent. 2. Screening Process: You’ll undergo a screening process to determine if you meet the specific eligibility criteria for the trial. These criteria may include age, gender, medical condition, medical history, and current health status. 3. Randomization and Assignment: If you meet the criteria and agree to participate, you may be randomly assigned to one of the treatment groups. This randomization ensures unbiased and fair comparisons between different treatments. 4. Study Procedures: Depending on the phase of the trial, you may receive the new treatment being tested, a standard treatment, or a placebo (if applicable). The trial’s procedures, including dosages, frequency of treatments, and follow-up visits, will be clearly explained to you. 5. Monitoring and Follow-up: Throughout the trial, you will be closely monitored by healthcare professionals. They will conduct regular check-ups, tests, and assessments to track your progress and the treatment’s effects. 6. Adherence to Protocol: It’s essential to follow the trial’s protocol and any instructions given by the research team. This consistency ensures the trial’s accuracy and reliability. 7. Possible Risks and Side Effects: Be aware of potential risks and side effects associated with the treatment. The research team will inform you about these during the informed consent process and will be available to address any concerns you may have during the trial. 8. Continued Medical Care: Even though you’re participating in a trial, you will continue to receive medical care for your condition. The research team will coordinate with your primary healthcare provider to ensure your well-being. 9. Privacy and Confidentiality: Your privacy will be protected, and your personal information will be kept confidential in accordance with ethical guidelines and privacy laws. 10. Open Communication: Feel free to communicate openly with the research team about any changes in your health, questions, or concerns. They are there to support and guide you throughout the trial. 11. Voluntary Participation: Remember that participating in a clinical trial is entirely voluntary. You have the right to withdraw from the trial at any time without any penalty or impact on your regular medical care. Clinical trials play a crucial role in advancing medical knowledge and improving patient care, and your participation contributes to these important efforts. Tandem Clinical Research takes great care to ensure your safety and well-being are the top priorities throughout the entire trial process.

Participating in a clinical research study offers several benefits, not just for the individual participant but also for the advancement of medical knowledge and the improvement of healthcare as a whole. Some of the key benefits include: 1. Access to New Treatments: Participants in clinical research studies often get access to cutting-edge treatments, drugs, or interventions that may not be available through regular medical channels. This provides an opportunity to explore potential benefits not yet widely accessible. 2. Advancing Medical Knowledge: By participating in research, individuals contribute directly to the expansion of medical knowledge. The data collected from the study helps researchers and healthcare professionals better understand diseases, their causes, and potential treatments. 3. Improved Personal Healthcare: The careful monitoring and follow-up involved in clinical research can lead to a deeper understanding of the participant’s health condition. This can result in better disease management and personalized healthcare recommendations. 4. Close Medical Supervision: Participants receive close medical supervision and attention from qualified healthcare professionals throughout the study. This frequent monitoring can identify health issues or concerns early on and allow for prompt intervention. 5. Helping Others: Clinical research studies are essential for finding new and better treatments for various medical conditions. By participating, individuals directly contribute to the development of therapies that may benefit future patients and improve overall public health. 6. Access to Expert Care: Clinical trials are often conducted at major medical centers and research institutions, where participants can receive care from expert healthcare providers and researchers. 7. Cost Savings: In some cases, participating in a clinical trial may reduce the cost of treatment, as the study sponsor may cover some or all of the expenses related to the trial. 8. Support and Education: Participants are provided with information and education about their condition and the treatment being studied. This empowers them to make informed decisions about their healthcare. 9. Opportunity for Rare Conditions: For individuals with rare or challenging medical conditions, clinical trials may offer one of the few opportunities to explore potential treatments tailored to their specific needs. 10. Contribution to Society: Being part of a clinical research study is a way of giving back to society and making a significant impact on the future of medicine and healthcare. It’s important to note that while there are many benefits, clinical research also involves potential risks, and not every study may be suitable for every individual. Before deciding to participate in a clinical trial, it is crucial to carefully review the study information, ask questions, and discuss with the research team and your healthcare provider to make an informed choice.

Current Studies

Obesity Research Study

Rhinosinusitis – Marrero

Continuous Glucose Monitor Study – Marrero

Atopic Dermatitis Research Study – Metairie

Why Tandem Clinical Research?

And the remedy starts with you! By participating in a clinical trial, you get the opportunity to access innovative treatments, advance medical knowledge, and contribute to improving healthcare for themselves and future generations.

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What people are saying about us online, check out our latest blog posts.

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Departments

Academic departments school of medicine anesthesiology biochemistry and molecular biology cell biology and anatomy dental medicine dermatology emergency medicine family and community medicine medicine neurology neurosurgery medical students medical research basic science research clinical research obstetrics and gynecology ophthalmology orthopedic surgery otolaryngology pathology, microbiology and immunology pediatrics pharmacology physiology psychiatry and behavioral sciences radiation medicine radiology rehabilitation medicine surgery urology school of health sciences and practice graduate school of biomedical sciences, administrative departments.

Clinical Research

The Department of Neurosurgery at Westchester Medical Center is a recognized leader among the academic neurosurgery community and is heavily involved in research and publication. Investigators within Neurosurgery are involved in the conduct of basic, clinical, and translational research. WMC Neurosurgery clinical faculty perform diverse research within their specialties. Ongoing projects represent a broad range of clinical questions in neurosurgery, with a focus on surgical outcomes and risk factor stratification. Frailty, or the overall health status of elderly patients, is one of the innovative areas of ongoing investigation along with strategies for avoidance in traumatic brain injury (TBI), neuro-oncology, cerebrovascular and spinal surgery, and neurocritical care. There is also a focus on clinical outcomes of subarachnoid hemorrhage and acute ischemic stroke, as well as the development of practice guidelines in the rapidly evolving field of neuroendovascular surgery. The research effort is supported by the neurosurgery residents and fellows along with nearly 50 medical students with the goal of creating a world-class, grant funded research enterprise.

Our current research initiatives are as follows:

Institutional Research

• PI: Chirag D. Gandhi, MD
• PI: Justin G. Santarelli, MD
• PI: Hasit Mehta, MD
• PI: Fawaz Al-Mufti, MD
• PI: Jared Pisapia, MD
• PI: Rachana Tyagi, MD
• PI: Merritt Kinon, MD

Sponsored Research Trials

• NCT03876457
• Sponsor: University Hospitals Cleveland Medical Center
• NCT04816591
• Sponsor: Cerenovus
• NCT04402632
• Sponsor: Medtronic
• PI: Justin Santarelli, MD
• NCT04852783
• Sponsor: Cereus Endovascular
• NCT03642639
• Sponsor: NovaSignal, Corporation

Humanitarian Use Device Research

• Sponsor: Stryker Neurovascular

NOTICE OF NONDISCRIMINATORY POLICY AS TO STUDENTS The New York Medical College admits students of any race, color, national and ethnic origin to all the rights, privileges, programs, and activities generally accorded or made available to students at the college. It does not discriminate on the basis of race, color, national and ethnic origin in administration of its educational policies, admissions policies, scholarship and loan programs, and athletic and other school-administered programs. See full non-discrimination statement with contact info .

Below are actively recruiting clinical trials for New York. Click on the closest city to find the research studies that are available in your area.

(151a) Northport

100 White Spruce Blvd, Rochester

1000 Tenth Avenue

1051 Riverside Dr, New York

1090 Amsterdam Avenue, Suite 11d New York

119 West 24th Street, Ground Floor, New York

1300 York Avenue, New York

140 East 80th Street New York, Ny 10075

160 East 34th Street, New York

177 Fort Washington Ave. New York

210 E. 64th. St. 8th. Floor

215 Lexington Avenue

300 East 66th Street, New York

317 East 17th Street Room 7f05 8th Floor

325 West 15th Street, New York

425 E. 61st Street, 8th Floor, New York

450 Clarkson Avenue, Brooklyn

462 1st Avenue

5 East 98th Street, New York

550 First Avenue Bcd 5, Room 558

622 W. 168th St.

75-59 262nd St, Glen Oaks

Annandale-on-hudson

Atlantic Beach

Ballston Spa

Basking Ridge

Binghampton

Binghamton,

Bingharmton

Borough of Staten Island

Bowmansville

Briarcliff Manor

Bridgewater

Brightwater

Brightwaters

Brooklyn Center

Burnt Hills

Canandaigua

Canandiaqua

Carle Place

Carmel Hamlet

Central Islip

Cheektowaga

Cherry Valley

Cities In New York

Clifton Park

Clifton Springs

Cold Spring Harbor

College Point

Columbia University Medical Center 710 West 168th Street,

Commack, Great Neck

Cooperstown

Cordtlandt Manor

Corlandt Manor

Cortland Manor

Cortlandt Manor

Cortlandtmanor

Cross River

Dobb's Ferry

Dobbs Ferry

E. Elmhurst

E. Setauket

E. Syracuse

East 34th Street, New York

East Greenbush

East Hampton

East Meadow

East Meadows

East Patchogue

East Setakuet

East Setauket

East Setaukey

East Steauket

East Syracuse

Eastchester

Elmira Heights

Erie, Niagara, and Chautauqua County

Far Rockaway

Farmingdale

Fatetteville

Fayetteville

Floral Park

Flushing Queens

Flushing, Queens

Forest Hills

Forrest Hills

Freash Meadows

Fresh Meadows

Gainesville

Garden City

Glenn Falls

Glens Falls

Grand Island

Guilderland

Hampton Bays

Hastings On Hudson

Hastings-on-hudson

Honeoye Falls

Hopewell Jct

Hopewell Jct.

Hopewell Junction

Hopwell Jct

Howard Beach

Huntington Station

Hvtn 722 West 168th Street Msph Bldg.

Jackson Heights

Jamaica Queens

Jefferson Valley

Johnson City

Kew Gardens

Lagrangeville

Lake Katrine

Lake Placid

Lake Success

Lake Success11042

Lake Sucess

Lindenhurst

Little Falls

Little Neck

Long Island

Long Island City

Loudonville

Loxahatchee

Manshasette

Massapequa Park

Mechanicville

Middle Village

Montefiore, Bronx Ny

Morrisville

Mount Cisco

Mount Kisco

Mount Sinai

Mount Vernon

Multiple Cities

Multiple Locations

N. Massapequa

N. New Hyde Park

N.massapequa

Nersey City

New Gardens

New Hartford

New Hyde Park

New Hyde Parkd

New Hyde Parke

New Rochelle

New Windsor

New York (2 Locations)

New York (6 Locations)

New York City

New York City,

New York City/westchester

New York Mills

New York Presbyterian Hospital

New York, Bronx

New York, Usa

Newhydepark

Ney Hyde Park

Niagara Falls

Niagra Falls

North Babylon

North Hills

North Massapequa

North Masspequa

North Syracuse

North Tonawanda

North Towanda

Not Confirmed

Not Predetermined

Oakland Gardens

Old Orangeburg

Old Westbury

One Gustave L Levy Place, Box 1410, New York

Orangeburg,

Orchard Park

Pearl River

Plattsburgh

Pleasantville

Port Chester

Port Jefferson

Port Jefferson Sta

Port Jefferson Station

Port Washington

Poughkeepsi

Poughkeepsie

Pougkeepsie

Queens Village

Richmond Hill

Rochester (2 Locations)

Rochester Hills

Rochester, Ny

Rochester, Ny 14620

Rockaway Beach

Rockville Center

Rockville Centre

Roslyn Heights

S. Setauket

Sackets Harbor

Saint Johnsville

Saranac Lake

Saratoga Springs

Saratogasprings

Schenectady

Seneca Falls

Sharon Springs

Skaneateles

Sleepy Hallow

Sleepy Hollow

Slingelands

Slingerland

Slingerlands

Smithtown and Port Jefferson

South Bronx

South Setauket

Southampton

Spring Garden

Spring Valley

Springfield Garden

Springfield Gardens

St. Johnsville

Stanton Island

Staten Island

Staten Island,

Stoney Brook

Stony Brook

Stony Brook,

United States

United States of America

Upper Nyack

Valley Cottage

Valley Stream

W. Brentwood

W. Henrietta

Wading River

Wappingers Falls

Ward's Island

Wards Island

West Babylon

West Harrison

West Haverstraw

West Hempstead

West Orange

West Sayville

West Seneca

Westchester

Westmoreland

White Plains

Wiliamsville

Willaimsville

Williamsville

Williston Park

Yorktown Heights

Ï»¿rochester

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Pathways to a Cure

Explore our 2023 annual report to learn about the ground-breaking innovations in cancer research and care happening here at Columbia.

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Cancer Types and Care

Cancer types, screening and outreach, screening and risk reduction, community outreach and engagement.

We work with our communities and patients to remove access barriers to cancer prevention, screening, treatment and survivorship services.

The Edward P. Evans MDS Center

The Edward P. Evans Center for Myelodysplastic Syndromes (MDS) takes an all-encompassing approach to the study and treatment of MDS.

Cancer Research Training and Education

We're dedicated to developing the next generation of researchers and physicians through cross-disciplinary training and fellowship programs

A Phase 3, Randomized, Double-Blind, Placebo- and Active-Comparator- Controlled Clinical study of Adjuvant V940 (mRNA-4157) Plus Pembrolizumab Versus Adjuvant Placebo Plus Pembrolizumab in Participants With High-Risk Stage II-IV Melanoma

Nct number:, study status:, population:.

The purpose of this study is to compare V940 plus pembro given after surgery to a placebo plus pembro given after surgery and to study how effective the study drug is. A placebo looks like a study drug, but it has no active ingredients. V940 has not yet been approved by the Food and Drug Administration (FDA). Pembrolizumab is FDA approved but it has not been approved for use with V940.

Are you Eligible? (Inclusion Criteria)

• Must be 18 years old or older - Cannot have ocular and/or mucosal melanoma - No COVID-19 and seasonal flu vaccines within 30 days before the first dose of the study drug

Specialty Area(s)

Principal investigator, benjamin izar, md, phd, trial location(s).

COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK

Clinical Research Coordinator

• Otolaryngology
• Columbia University Medical Center
• Opening on: May 17 2024
• Job Type: Officer of Administration
• Bargaining Unit:
• Regular/Temporary: Regular
• End Date if Temporary:
• Hours Per Week: 35
• Standard Work Schedule: Monday-Friday (9AM-5PM)
• Salary Range: $62,400.00-$68,000.00

Position Summary

The Department of Otolaryngology is seeking an individual for the position of Clinical Research Coordinator (CRC) who is passionate about delivering high-quality work. The CRC will have strong organizational, multi-tasking, time management, communication, and interpersonal skills to join the Clinical Research Core in executing clinical trials for improving treatments and outcomes for patents. The position is responsible for collaborating with PIs, team members, clinicians, and sponsors as well as working independently. The CRC will report directly to the Research Manager and Director of Clinical Trials. The main role of the CRC will be to operate and maintain the day-to-day operational duties of their assigned clinical trials and clinical research study database. 

Responsibilities

• Clearly and effectively communicate with potential study subjects, clinicians, and other health care providers, ancillary staff, sponsors, and research office staff.
• Work with Regulatory team in submitting new protocols, amendments, renewals and other regulatory bodies.
• Work with Program Manager in preparation of study budgets, submitting pharmacy cost estimates, ensuring compliance with research billing and processing stipends for subjects’ participation in studies.
• Coordinate day-to-day aspect of study related procedures, including, but not limited to scheduling visits and procedures, data entry, preparation for research visits, research visit documentation, maintenance of regulatory binders and study files, creation and/or maintenance of source documentation, and preparation for monitoring visits, site initiation/closeout visits and audits as needed.
• Prepare for, participate in, contribute to meetings with the Core, PIs, and Sponsors.
• Other duties as assigned.

Minimum Qualifications

• Bachelors degree and or equivalent in education and experience. 

Preferred Qualifications

• 2 years of related experience.
• Proficient in Spanish.

Other Requirements

• Complete and maintain the required training for participation in clinical research, including but not limited to, Human Subjects Protection training and Clinical Research Coordinator Course.
• Candidate will ensure integrity and compliance with all regulatory, institutional, and departmental requirements.
• The ability to take initiative and work independently.
• The ability to effectively work in a complex matrix.
• Outstanding technical writing skills and understanding of medical terminology/research.
• Advanced understanding of data management processes.
• Ability to analyze and interpret scientific data and skilled in the use of computerized systems and databases.
• Ability to understand and follow scientific research protocol and procedure.
• Excellent communication skills (both verbal and written).
• Exceptional organizational, interpersonal, and presentation skills.
• Ability to understand and follow complex, detailed technical instructions.
• Ability to foster a cooperative and collaborative work environment.
• The ability to be flexible with scheduling is mandatory; willingness to work evenings and weekend hours in unusual or emergent situations.
• Knowledge of MS Office, specifically Word and Excel.

Equal Opportunity Employer / Disability / Veteran

Columbia University is committed to the hiring of qualified local residents.

Commitment to Diversity 

Columbia university is dedicated to increasing diversity in its workforce, its student body, and its educational programs. achieving continued academic excellence and creating a vibrant university community require nothing less. in fulfilling its mission to advance diversity at the university, columbia seeks to hire, retain, and promote exceptionally talented individuals from diverse backgrounds.  , share this job.

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Im prove Healthcare with You r care er

Clinical research intern, new york, new york.

As an intern with Fresenius Medical Care, a student will apply classroom based knowledge to workplace experience and will benefit from learning experiences in their major area of study.

Supports FMCNA’s mission, vision, core values and customer service philosophy.  Adheres to the FMCNA Compliance Program, including following all regulatory and division/company policy requirements.

PURPOSE AND SCOPE:

Under supervision, the Clinical Research Intern will assist in carrying out research activities related to clinical research. In addition, they will be given the opportunity to enhance their research skills by working with our diverse team of researchers. The Clinical Research Intern will become more familiar with renal (patho)physiology, renal replacement therapies, and research being done to improve patient outcomes.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

• Under close supervision, utilizes established procedures to perform routine assigned research tasks
• Learns to use good clinical practice and research integrity concepts
• Applies company policies and procedures to resolve routine issues
• Works on problems of limited scope. Follows standard practices and procedures in analyzing situations or data from which answers can be readily obtained
• Conducts literature reviews
• Assists in the preparation of study-related materials, including screening forms, case report forms and questionnaires
• Assists in medical record review
• Under supervision, assists in the recruitment of study subjects
• Assists in the collection and analysis of data
• Organizes, maintains, and updates project-related files and databases
• Attends routine project meetings
• Attends seminars and other meetings as necessary
• Builds stable working relationships internally
• Escalates issues to supervisor/manager for resolution, as deemed necessary
• Assists with various projects as assigned by direct supervisor
• Other duties as assigned

PHYSICAL DEMANDS AND WORKING CONDITIONS :

• The physical demands and work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
• Day to day work includes desk and personal computer work as well as interaction with study subjects and clinic personnel. The position requires travel to participating research sites in New York City.
• Enrolled in a bachelor’s degree program, with a minimum of 1 year of undergraduate program completed, preferably with a focus in healthcare, research, biology, chemistry, mathematics, or engineering

EXPERIENCE AND REQUIRED SKILLS :

• 0 - 2 years’ related experience preferred

EO/AA Employer: Minorities/Females/Veterans/Disability/Sexual Orientation/Gender Identity

Fresenius Medical Care North America maintains a drug-free workplace in accordance with applicable federal and state laws.

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York Biomedical Research Institute

University of York launches new centre for blood disorder research

The University of York is today (11 July) launching the Centre for Blood Research - a pioneering initiative bringing together for the first time a diverse community of researchers and clinical staff.

The new centre will further our understanding of blood cancers and disorders and aims to translate research into the clinical setting - eventually leading to possible new treatments.

It is believed to be one of the first centres in the UK and Europe to bring together expertise in experimental haematology, population epidemiology and clinical settings.

Research funding

The centre, based across the departments of Biology, Health Sciences and Hull York Medical School, already leads a significant research portfolio with more than £22m in active research funding, including grants from Medical Research Council, Cancer Research UK, Bill and Melinda Gates Foundation and Blood Cancer UK.

Blood cancer is currently the UK’s third biggest cancer killer, with over 41,000 people being diagnosed with it every year and unlike most other cancers, it can affect people at any age, from birth through to old age.

The new centre will research the health experiences of the general population and spans the full spectrum – from causes through to their consequences.

The centre’s director, Professor Ian Hitchcock, said any medical breakthroughs in clinical care are often underpinned by fundamental biological and epidemiological research.

He said: “CBR has an ambitious vision to catapult Yorkshire and the Humber to the forefront of blood research.

“It brings together a thriving diverse community of researchers, technicians, administrators, software engineers and PhD students.

“One in every 16 men and one in every 22 women will develop blood cancer at some point in their lives and patients are at the core of what we do - with the ultimate aim of translating our research into the clinic.

“This is an unique opportunity for York and CBR, working together to make a real world difference for patients and their treatments.”

Clinical trials

Professor Adele Fielding is the Centre’s clinical director and has joined the University of York and Hull York Medical School specifically to take up this role. She works on acute lymphoblastic leukaemia throughout the translational research cycle from large clinical trials to basic mechanistic work. She will see patients at Hull University Teaching Hospital.

She said: “I’m incredibly excited to join the team at York. The overall goal of my work is to improve the outcome for adults with acute lymphoblastic leukaemia. By joining CBR, where the three cornerstones of blood research  - basic science, clinical trials and epidemiology work together so well, I hope we can move a step closer to realising this goal together.” 

University of York Vice-Chancellor Professor Charlie Jeffery said: “In bringing together experts in experimental, clinical and population studies, we have created a unique environment in which to understand the full scope of blood diseases, allowing our team to innovate and create solutions, but to also influence health policy, reduce inequalities, and create a true picture of how people’s lives are impacted.”

Better treatments

Blood Cancer UK’s CEO, Helen Rowntree, said: "Yorkshire is where Blood Cancer UK began, and now we're thrilled to mark the launch of the Centre for Blood Research at the University of York. As researchers delve deeper into how blood cells turn cancerous, we move closer to unlocking better treatments for people with this disease.

  “Blood cancer is the UK's fifth most common type of cancer, and includes those living with leukaemia, lymphoma, and myeloma. There are advantages to harnessing commonalities between the diseases and bringing people and research funding together. And with this centre's mission to explore the full spectrum of blood diseases, looking from their origins to their consequences, it will bring us closer to a day where no lives are lost to blood cancer.”

• Blood cancer is the fifth most common cancer in the UK
• It is the most common type of childhood cancer. Every year, more than 500 children aged under 15 are diagnosed with blood cancer. Of these, about 400 have childhood leukaemia and about 100 have lymphoma.
• The risk of blood cancer goes up as you get older, and just under 40% of people diagnosed with it are aged 75 or over.

Learn more about the Centre for Blood Research