593 Results for

Clinical Research Jobs in Cooper, NY

Jobs

New!

New York, NY4 days ago

$120,000–$140,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations.

New!

Hoboken, NJ4 days ago

$350,000–$400,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. 4. Collaborate with cross-functional teams including regulatory affairs, pharmacovigilance, and medical affairs to ensure a holistic approach to product development.

Livingston, NJ11 days ago

Our partnership with Rutgers University creates the state’s largest academic healthcare system dedicated to providing high-quality patient care, leading-edge research, and world-class health and medical education, further advancing our mission of providing high-quality healthcare in New Jersey. CBMC is located in Northern New Jersey in Essex County, which is an ideal location to reside with easy access to the Jersey Shore, NYC, beautiful suburban neighborhoods, diverse communities, and top-notch school districts -- plus access to museums, fine dining and great shopping!

New!

Rahway, NJ1 day ago

$45–$53.45 Per Hour

Serve as a subject matter expert in immunoassay-based assay development and validation, collaborating with project teams, biomarker leaders, clinical operations and regulatory affairs on the implementation of these assays in clinical trials. Translational Molecular Biomarkers (TMB) is responsible for the development and execution of clinical biomarker assays across all therapeutic areas and all phases of clinical development within our company's research laboratories.

New Brunswick, NJ11 days ago

RWJBarnabas Health, the largest and most comprehensive integrated healthcare system in New Jersey, and a proud partner of Rutgers Cancer Institute of New Jersey—New Jersey’s only NCI-designated Comprehensive Cancer Center—is actively recruiting a full-time Attending Medical Oncologist specializing in Genitourinary (GU) Malignancies to join our dynamic oncology team. Our partnership with Rutgers University creates the state’s largest academic healthcare system dedicated to providing high-quality patient care, leading-edge research, and world-class health and medical education, further advancing our mission of providing high-quality healthcare in New Jersey.

Jersey City, NJ13 days ago

Collaboration: Develop and nurture professional relationships with physicians and staff at JSUMC and other Hackensack Meridian Health (HMH) campuses, including Ocean University Medical Center (OUMC), to promote practice growth to Bayshore Medical Center (BMC). ? The posted rate of pay in this job posting is a reasonable good-faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.

East Brunswick, NJ13 days ago

Hematologist Opportunity Astera Cancer Care East Brunswick/Monroe, NJ Job Details: Occupation: Physician Specialty: Hematology Clinic Location: East Brunswick/Monroe, NJ Employment: Full-Time Opportunity: Private Practice, Outpatient/Inpatient Board Certifications: BE/BC Degree: MD/DO Ideal Candidate: ~ Open to Fellows and Experienced Physicians About the Role: Astera Cancer Care is seeking a board-certified or board-eligible Hematologist with expertise in both malignant and benign hematologic disorders to join our dynamic and collaborative team. The ideal candidate will provide compassionate, evidence-based care to patients with a wide spectrum of hematologic conditions, including hematologic malignancies (e.g., leukemia, lymphoma, myeloma, and CAR-T) and non-malignant disorders (e.g., anemia, thrombocytopenia, sickle cell disease, bleeding/clotting disorders).

New!

Queens, NY6 days ago

$362,418–$470,000 Per Year

Queens Hospital was recognized at ASCOs plenary session for their research efforts in enrolling patients in a diverse community and we welcome candidates who are interested in being an investigator in clinical trials for cooperative group studies, pharmaceutical studies and/or physician-initiated studies where you will have the full support of our knowledgeable research staff for both regulatory and clinical needs. State-of-the-art facilities include a total of three DaVinci Xi surgical robots, two at Elmhurst and one at Queens, multiple PAs/NPs and urology residents at each site, both are COC-designated Cancer Centers of Excellence, and Elmhurst is a Level 1 Trauma Center.

New York, NY15 days ago

$25–$30 Per Hour

The Rogosin Institute is an independent not-for-profit medical care and research organization affiliated with New York Presbyterian Hospital and Weill Cornell Medicine. Under the supervision of a registered nurse, the Clinical Assistant participates in the delivery of patient care services by direct patient care and supportive services.

Summit, NJ17 days ago

$30–$35 Per Year
Full-time
Employee

Work closely with cross-functional teams, including other R&D functions, Commercial Marketing, Quality Assurance, Regulatory Affairs, and Manufacturing, to achieve project goals. Prepare and maintain detailed documentation for product development processes, including experimental protocols, and technical reports in compliance with Good Documentation Practices (GDP).

New!

Paramus, New Jersey4 days ago

Schedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit. Responsibilities: A day in the life of a Clinical Research Coordinator at Hackensack Meridian Health includes: Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.

Hackensack, New Jersey15 days ago

Responsibilities: Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. Performs nursing assessments and monitors study patient`s progress during clinical trials; Tracks study patient`s response by documenting on toxicity flow sheet, medication flow sheet and nurses` progress notes.

New York City, NY30+ days ago

$85,000–$90,000 Per Year

Oversee investigational product (IP) accountability across all assigned trials, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal; ensure compliance with protocol, regulatory requirements, and site SOPs, and provide guidance and oversight to CRCs and RAs supporting IP management. Serve as the primary operational lead for study start-up activities, including SIV and PSV readiness, document preparation, development of site workflows, staff training completion, and management of study supplies.

New York City, NY30+ days ago

$31.97–$33.17 Per Year

Maintain investigational product (IP) accountability for assigned studies, including receipt, storage, dispensing, reconciliation, temperature monitoring, documentation, and proper disposal, ensuring compliance with protocol, regulatory requirements, and site SOPs. This role is ideal for coordinators with experience managing one or more trials, supporting day-to-day study operations, and working collaboratively with research staff under guidance from senior team members.

Long Island, NY25 days ago

Founded in 2021, SiteBridge Research is an integrated research organization, focused on building a national network of small and community medical practices to deliver world-class industry-sponsored clinical research studies on time and on budget, accelerating time to completing clinical trials, accelerating time to market and product adoption in communities that are often underrepresented and difficult to reach. The SiteBridge Network extends reach further into these communities to empower patients with some of the highest unmet needs to take part in clinical studies to improve inclusivity in clinical research and to improve overall health outcomes.

Hawthorne, New York30+ days ago

Overview: Responsible for pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data collection and management, adverse event management to ensure protocol compliance in conjunction with the PI, clinical team and clinical research nurses and team. Enter data on Hematology, Oncology and Stem Cell Transplant patients on electronic data capture forms; prepare for routine data audits and maintain source documents and regulatory binders.

Bronx, NY30+ days ago

$20–$25 Per Hour

This role focuses on the hands-on execution of essential administrative and clinical tasks—such as scheduling, preparing visit materials, supporting participant flow, maintaining source documentation, and completing timely data entry—to ensure efficient site operations and high-quality study conduct. The enrollment RA works closely with the enrollment coordinators to provide insights that inform clinical judgment on participant eligibility and study suitability and assists with screening activities and accurate documentation in compliance with ICH-GCP, study protocols, and regulatory requirements.

New York, NY7 days ago

$70,481.61–$75,000 Per Year

The Clinical Research Coordinator performs study coordination tasks under the direction of the Principal Investigator and works closely with the Research Nurses to ensure overall compliance in the conduct of the study, and adherence to the approved study protocol. Prepare for study visits: bio-specimen collection, research ticket preparation, lab and EKG orders, scheduling of imaging scans, AE and Conmed form completion in conjunction with licensed professional and other tasks as needed.

New Brunswick, NJ30+ days ago

Full-time

Responsibilities:Under supervision of clinical research leadership staff, the medical staff, and in collaboration with research nurse staff, performs protocol-specific tasks including patient screening, ordering tests, collecting specimens and study documentation of patient reported responses, relative to various Phase 1 Oncology trials. IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP.

New York, New York30+ days ago

$48–$52

The CCRC will play a critical role in ensuring the ethical, regulatory, and operational integrity of clinical trials while supporting investigators, participants, and sponsors in a highly organized and patient-centered environment. That is why we offer early morning and after work hour appointments at our conveniently located Murray Hill office in New York City.

New York, NY8 days ago

$45–$47

Job Title: Clinical Research CoordinatorLocation: New York, NY 10021 Duration: 12+ Months Job Type: Temporary Assignment Work Type: OnsiteJob Description: As an integral member of the Clients research team and in compliance with all regulatory, institutional, and departmental requirements, performs data collection, data entry and data analysis for research projects, databases, and research protocols within Client. Performance Expectations: Performs abstraction of data from source records in patient/human subject records (e.g., electronic medical record, laboratory or diagnostic test results, surgical/radiation treatments delivered); abstraction of data from publications, or data collection from outside physicians' offices.

New York, NY8 days ago

$70,481.61–$75,000

New York, NY30+ days ago

$70,481.60–$75,428.87 Per Year

Director Clinical Research Finance to prepare Cancer Center expense budgets associated with clinical trials revenue and expense for upcoming fiscal year, based on professional judgment and a projection of direct and indirect costs and fee revenue for open and pending trials. Director Clinical Research Finance, ensures fiscal compliance to trial sponsor and institutional policies and procedures, and ensures that the departments fiscal interests are served in the conducting of oncology clinical trials.

Teaneck, NJ30+ days ago

$50,003.20–$67,496 Per Year
Full-time

The Coordinator oversees study activities from start-up through close-out, including regulatory submissions, participant screening and enrollment, study visit coordination, data and document management, and ongoing communication with investigators, sponsors, IRBs, and internal clinical teams. Holy Name is New Jersey's only independent Catholic health system, comprising a 361-bed acute care hospital, a renowned cancer center, a state-of-the-art fitness center, a residential hospice, a prestigious nursing school, and an extensive physician network.

New Brunswick, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that requires all on-site resources such as prospective Vitalief consultants to provide proof that they are fully vaccinated for Covid-19; inoculated annually for Influenza; and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNP. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

Rahway, NJ22 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

Rahway, NJ18 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. By blending deep subject matter expertise with strong business acumen, we deliver Consulting and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

Valhalla, New York30+ days ago

The individual will be responsible for the oversight of studies conducted out of the clinical trials unit, and as such, will be responsible for contracts, oversee the research coordinators and study progress reports, orders, and other tasks as needed. Drive internal communication, including timelines, budget, progress, and project needs for clinical trials to product teams and senior management.

Brooklyn, New York18 days ago

$56,000–$71,000 Per Year

The system is anchored by Maimonides Medical Center, one of the nation’s largest independent teaching hospitals and home to centers of excellence in numerous specialties; Maimonides Midwood Community Hospital (formerly New York Community Hospital), a 130-bed adult medical-surgical hospital; and Maimonides Children's Hospital, Brooklyn's only children's hospital and only pediatric trauma center. About Us: We’re Maimonides Health, Brooklyn’s largest healthcare system, serving over 250,000 patients each year through the system’s 3 hospitals, 1800 physicians and healthcare professionals, more than 80 community-based practices and outpatient centers.

New York, NY30+ days ago

$101,493.51–$107,250 Per Year

This position will work collaboratively with the Regulatory Specialist and Principal Investigators to ensure adherence to research protocols and compliance with FDA regulations, HIPAA, GCP and institutional policies, and assist with recruitment, enrollment, grant submissions, research data collection and study coordination. This may include abstraction of data from the patient chart (e.g., laboratory or diagnostic test results, surgical/radiation treatments delivered, adverse drug reactions, etc); abstraction of data for publications, or data collection from outside physicians offices.

New!

Parsippany, NJ1 day ago

$178,000–$210,000 Per Year

Responsibilities: Contribute to and support the company’s efforts in communicating the high value of Ferring Uro-oncology research initiatives to successfully execute trial needs Initiate and maintain relationships with study investigators to create advocates for Ferring Uro-Oncology research Collaborate with the Therapeutic area medical team and medical affairs to support current PI involvement and KOL engagement initiatives Uncover opportunities for engagement to ensure appropriate enrollment at each research center Collaborate with Ferring clinical operations, TA medical directors, and CRO to identify and develop key performance indicators (KPIs) for activities aimed at enhancing trial recruitment, and ensure reports are developed and shared with management to track progress and drive improvements Work with Ferring clinical operations, TA Medical Directors and CRO to understand KPIs for enrollment and support where necessary for optimal study performance – then delete this as incorporated in above Work to facilitate collaboration between different departments or groups within the same study site to optimize the enrollment of trial participants, feeding back any trial-specific impact to the Ferring clinical operations team to ensure coordinated efforts Report identified site or vendor issues to Clinical trial team via TA medical directors including opinions and observations related to the operational, scientific and other aspects of the study so that Ferring clinical operations team can assess appropriate trial-related actions Collaborate with Ferring medical affairs and CTT during the start-up phase for selection of sites to enable and retain beneficial experiences and best practices Ensure alignment of medical communications and publications plans within the overall medical brand and development plan – delete as this has too much overlap with existing teams and processes Support and partner with key internal business partner Ensure effective interaction & communication between the uro-oncology research team, medical science liaison teams and other key stakeholders Requirements: Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 15+ years in matrix leadership organizations in operational or client facing environments. Experience working with Urologist preferred Prior medical affairs, medical communications, publications and/or KOL management experience highly desired Proven leadership track record with exceptional communication, collaboration and prioritizing skills, supporting pre and post-launch activities.

New York, New York30+ days ago

Overview: Reporting to the Clinical Trials Nurse Manager, the Clinical Research Nurse is responsible for emphasizing screening, enrollment, treatment administration, and data collection while ensuring compliance and patient safety in the Diagnostic and Treatment Center (D&TC). The salary of the finalist selected for this role will be set based on various factors, including but not limited to organizational budgets, qualifications, experience, education, licenses, specialty, and training.

New York, NY30+ days ago

$101,493.51–$107,250

New York, NY8 days ago

$53,294.22–$57,750
Temporary

Works with departments, labs, other personnel and areas as needed, to ensure the timely transfer of items and biological materials: study drugs; histology slides; serum, urine, blood samples, etc., using appropriate precautions at all times. Works with School of Medicine and Medical Center staff and departments, including Directors, Managers, Clinical Information Systems, Research Nursing and Regulatory Services; may also interfaces with patients and their families.

Parsippany-Troy Hills, NJ30+ days ago

$150,000–$175,000 Per Year

By providing your phone number, you consent to: (1) receive automated text messages and calls from the Judge Group, Inc. and its affiliates (collectively "Judge") to such phone number regarding job opportunities, your job application, and for other related purposes. Identify gaps in pre-clinical and Phase 1 DDP that could impact Phase 2/3 design and execution timelines for company internal projects as well as programs being evaluated as part of due diligence.

New York, NY30+ days ago

$100,000–$120,000

The primary purpose of the subspecialized oncology clinical research nurse role is to facilitate positive outcomes of safety and quality for patients enrolled on adult oncology clinical trials at the NYU Perlmutter Cancer Center by coordinating and managing patients enrolled on clinical trials by employing the nursing process, clinical skills, critical thinking, evidence-based nursing and an understanding the scientific research. 2. Utilizing the nursing process, nursing assessment skills and critical thinking the Oncology CRN I conducts a thorough research screening visit for potential trial participants per the protocol requirements, including but not limited to a Review of Systems (ROS), baseline and ongoing AE assessment and documentation, and collection of concomitant medications and documents the assessments in the EPIC electronic health record per CTO policies and procedures.

Piscataway, NJ19 days ago

$250,000–$275,000 Per Year

Develop new clinical indices and biochemical assessments and apply a broad range of established dental assessment indices (e.g., caries, plaque, gingivitis, periodontology, sensitivity, whitening, calculus, oral malodor, anti-bacterial or others) to design, evaluate, and differentiate clinical programs and product performance that are superior to, existing products. The ideal candidate is an internationally renowned expert in oral health and dental clinical research, with substantial industry and/or academic experience, a proven track record of leading clinical programs, and demonstrated strength in people leadership and collaborative partnerships.

New Brunswick, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. Vitalief partners with Sponsors, CROs, and research sites across the clinical trials ecosystem, delivering consulting and workforce solutions that improve efficiency, reduce costs, and accelerate patient-impacting innovation.

New Brunswick, NJ7 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. This position is ideal for oncology nurses currently working in direct patient care roles, whether in a hospital or outpatient setting, who are interested in transitioning into clinical research.

New Brunswick, NJ7 days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. This position is ideal for oncology nurses currently working in direct patient care roles, whether in a hospital or outpatient setting, who are interested in transitioning into clinical research.

New Brunswick, NJ20 days ago

Remote

Part-time

The ideal candidate brings deep expertise in organizational transformation and change management within complex healthcare and research environments, with a proven ability to drive stakeholder alignment, operational adoption, and sustainable process improvement across multi-site systems. Conduct in-depth interviews with clinical research staff and stakeholders across the clinical trial lifecycle to identify operational gaps, bottlenecks, communication challenges, and improvement opportunities across Oncology and Non-Oncology programs.

New Brunswick, NJ30+ days ago

Remote

Full-time

Proven success in building strong executive-level and C-suite relationships while leading a multi-faceted change process; demonstrated broad-based change management expertise and extensive experience positively influencing change in a variety of complex environments with multiple stakeholders and competing priorities. By blending deep subject matter expertise with strong business acumen, we deliver consulting (both operational and strategic) and Functional Service Provider (FSP) solutions that empower organizations to do more with less, streamlining operations, reducing costs, and accelerating breakthroughs that ultimately benefit patients. .

New Brunswick, NJ30+ days ago

Remote

Part-time

This role will serve as the primary subject matter expert (SME) for a comprehensive current-state operational assessment across Technology, Organization, Process, People, and Finances, with a strong focus on Non-Oncology programs and cross-system communication effectiveness. Conduct in-depth interviews with clinical research staff and stakeholders across the trial lifecycle to identify gaps, bottlenecks, and improvement opportunities for Non-Oncology operations.

New York City, NY30+ days ago

$34–$44 Per Hour

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Study Operations & Data Management: Accurately document all procedures and results in approved systems (e-source, logs, etc.) according to ALCOA-C++ and ensure regulatory compliance (GxP, HIPAA).

New York City, NY30+ days ago

$34–$44 Per Hour

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. As a Clinical Research Assistant, PRN (Registered Nurse) you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.

Orange, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. As the primary subject matter expert (SME), this leader will collaborate closely with the Vitalief delivery team to design and implement enterprise-level operational initiatives, with a strong emphasis on Non-Oncology programs and enhancing cross-system communication and coordination.

Orange, NJ30+ days ago

Full-time

IMPORTANT NOTE:Vitalief partners with clients such as major medical centers and academic institutions that often requires all on-site resources such as prospective Vitalief consultants to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis. #LI-DNPPowered by JazzHR. As the primary subject matter expert (SME), this leader will collaborate closely with the Vitalief delivery team to design and implement enterprise-level operational initiatives, with a strong emphasis on Non-Oncology programs and enhancing cross-system communication and coordination.

Brooklyn, NY17 days ago

$25–$35

Demonstrated experience applying core research methods (user interviews, workflow observation, surveys, qualitative and quantitative analysis) in a substantive project, such as a graduate thesis, lab study, applied internship, or industry engagement. Master's or PhD candidate (or recent graduate) in a research-heavy field, for example public health, health informatics, anthropology, behavioral or cognitive science, psychology, human factors, or related.

New York City, NY30+ days ago

$102,000–$120,000 Per Year

Our teams primarily operate from the New York Metropolitan area, NY, and remotely via San Francisco/Bay Area, CA, Seattle, WA, Boston, MA, Chicago, IL, and Washington, D.C. For those in our New York City office, we encourage in-person collaboration by requiring team members to work onsite three days a week (Tuesday, Wednesday, Thursday). Maven is looking for an enthusiastic and collaborative Senior Clinical Research Analyst to help us analyze, evaluate, and communicate how Maven's world-class support for women and families impacts clinical outcomes (e.g., preterm birth, mental health, conception).

Piscataway, NJ18 days ago

$250,000–$275,000 Per Year

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Clinical Research Jobs in Cooper, NY

Sr. Oncology Clinical Research Associate Jobot

Vice President Clinical Development Ophthalmology Jobot

Director, Pediatric Intensive Care Unit (PICU) - Cooperman Barnabas Medical Center RWJBarnabas Health | Livingston, New Jersey RWJBarnabas Health

Scientist - II Nesco Resource

RWJBarnabas Health is Seeking a Medical Oncologist in Central and Northern New Jersey RWJBarnabas Health

Urogynecologist Hackensack Meridian Health

Physician - Hematology and Oncology - Medical Oncologist/Hematologist OneOncology

Associate Director of Urology Mount Sinai Services of the Icahn School of Medicine at Mount Sinai--Elmhurst and Queens Programs

Clinical Assistant The Rogosin Institute

Research & Development, Scientist 2 YANTRAN LLC

Clinical Research Coordinator Hackensack Meridian Health

Clinical Research Nurse - Phase 1 - P/T with Benefits - Days Hackensack Meridian Health

Clinical Research Coordinator III Adams Clinical

Clinical Research Coordinator II Adams Clinical

Clinical Research Coordinator SiteBridge Research, Inc.

Clinical Research Associate New York Medical College

Clinical Research Enrollment Assistant Adams Clinical

Clinical Research Coordinator NYU Langone Medical Center

Senior Clinical Research Coordinator Vitalief

Clinical Research Coordinator - Part Time Bethany Medical Clinic

Clinical Research Coordinator TekWissen LLC

Clinical Research Coordinator NYU Langone Health

Financial Coordinator - Clinical Research NYU Langone Medical Center

Clinical Research Coordinator-Full-time-Onsite Holy Name Medical Center

Clinical Research Coordinator Vitalief

Clinical Research Coordinator (CRC) – Infectious Disease Vitalief

Clinical Research Coordinator – Cardiovascular Vitalief

Clinical Research Project Manager New York Medical College

Clinical Research Coordinator Maimonides Medical Center

Research Nurse, Cardiology Clinical Trials NYU Langone Medical Center

Director, Clinical Research Alliances Ferring Pharmaceuticals, Inc.

Clinical Research Nurse | Diagnostic & Treatment Center Rockefeller University

Research Nurse, Cardiology Clinical Trials NYU Langone Health

Clinical Research Assistant NYU Langone Health

Associate Director Clinical Research & Development Judge Group

Clinical Research Nurse I - Oncology NYU Langone Health

Sr. Director, Clinical Research (Piscataway, NJ, US) Colgate-Palmolive Company

Oncology Clinical Research Nurse Director Vitalief

Oncology RN – Clinical Research Nurse (Training Provided) Vitalief

Oncology Nurse (RN) – Clinical Research Career Opportunity Vitalief

Clinical Research Change Management Consultant Vitalief

Vice President, Clinical Research FSP Consulting Vitalief

Clinical Research Strategic Management Consultant Vitalief

Clinical Research Assistant, PRN Care Access

Clinical Research Assistant, PRN (Bilingual, Registered Nurse) Care Access

Director, Clinical Research Operations Transformation Vitalief

Senior Director, Clinical Research Operations Vitalief

Clinical Product Research Intern Norbert Health

Senior Clinical Research Analyst Maven Clinic

Sr. Director, Clinical Research Colgate-Palmolive

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