1,598 Results for

Clinical Jobs in Woodhaven, NY

Jobs

New York, NY9 days ago

$350,000–$400,000 Per Year

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New York, NY7 days ago

$120,000–$140,000 Per Year

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New!

New York, NY2 days ago

$105,000–$122,000 Per Year

This role partners closely with hospital teams, physicians, case managers, and interdisciplinary hospice professionals to evaluate patients for hospice services, coordinate admissions, provide inpatient hospice support, and ensure patients receive exceptional end-of-life care. 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.

New!

Brooklyn, NY1 day ago

$88,000–$98,000 Per Year

This role provides direct clinical services to adolescent and adult patients our primary care and school-based clinic settings. Description:BMS Family Health Center is seeking a compassionate and dedicated Licensed Clinical Social Worker (LCSW) to join our behavioral health team.

New York City, NY12 days ago

$101,000–$152,000 Per Year
Full-time

Reviews and assesses applicable financial, clinical, and operational data, as well as evidence-based literature to assist teams in evaluating new supplies and new technology, using evidence based clinical data, benchmarked best practices and data driven analysis. Participate as a clinical team representative on project teams, committees and in meetings with various corporate departments to provide input as to the clinical perspectives on products and issues.

New!

Stamford, CT1 day ago

$104.63–$104.63 Per Hour

This highly visible leadership role offers the opportunity to oversee study strategy, enrollment, budgets, CRO partnerships, and cross-functional teams while influencing clinical development decisions on a global scale. Joulé is partnering with a leading pharmaceutical organization seeking an experienced Associate Director, Clinical Development Trial Lead to drive the execution of complex global oncology clinical trials.

New!

Jersey City, NJ4 days ago

The Clinical Development Executive Medical Director is the clinical leader of the specific clinical programs assigned with responsibility for outlining the overall clinical development strategy in line with regulatory requirements and sound scientific rationale, designing the clinical protocols, guiding the Clinical Operations team towards the adequate implementation of such protocols, ensuring adequate medical monitoring activities are implemented for the conduction of clinical studies and analyzing the data from the clinical program. The individual will also be responsible for ensuring adequate implementation of the global safety surveillance and pharmacovigilance for the investigational products, including review and analysis of safety data from clinical trials and other permitted sources (e.g., early access/expanded access programs, if applicable), identification and investigation of safety signals, and management of the benefit-risk profile for assigned compounds.

Manhattan, NY9 days ago

$145,000–$168,000 Per Year

We’re bringing the world’s top spine surgeons together to create the Spine Hospital delivering an innovative, patient-inspired experience that will transform patient care. Make a difference in the lives of your patients and feel the reward of your career at the newest and most advanced Spine Hospital in the world.

Jericho, NY13 days ago

This individual will work under the direction of the supervisor of the team performing clinical reviews and abstractions of assigned cases related to a maternal death or to an adverse event that occurred during an outpatient surgical procedure. Impactful Work: Contribute to a mission-driven organization dedicated to improving patient outcomes by identifying and analyzing critical events in maternal care and outpatient surgical procedures.

Brooklyn, NY12 days ago

$145,000–$168,000 Per Year

As the Clinical Nurse Manager, you will manage patient care delivery within Perioperative Services, serving as a clinical resource and administrator in the absence of unit leaders or when care-related issues arise. In collaboration with the Patient Care Director, the Clinical Nurse Manager will participate in the establishment of the units short and long term goals and ensures its alignment with the hospital’s overall strategic goals.

New!

Bronxville, NY5 days ago

$145,000–$168,000 Per Year

At NewYork-Presbyterian, nursing is a life-changing career journey focused on amazing patient outcomes every step of the way. This is a full-time night position covering the hours of 7:00pm – 7:00am at NewYork-Presbyterian Westchester located in Bronxville, right across from the Metro North Station.

Manhattan, NY7 days ago

$145,000–$168,000 Per Year

Here, courageous nurses administer chemotherapy, manage symptoms, support patients and educate families, all while serving as the nerve center of extensive multidisciplinary teams. Work in collaboration with the Patient Care Director, participate in the establishment of short and long term goals and ensure its alignment with the hospital’s overall strategic goals.

New!

Manhattan, NY5 days ago

$145,000–$168,000 Per Year

Join us, and manage the delivery of high-quality care to patients in the Cardiac Medicine Telemetry Stepdown at New York-Presbyterian Hospital/Weill Cornell Medical Center. 2026 America’s Greatest Workplaces for Culture, Belonging & Community – Newsweek.

Manhattan, NY7 days ago

$145,000–$168,000 Per Year

As the Pediatric Service Line Clinical Manager, you will lead a Magnet designated nursing team and collaborate with the transformational leaders of the entire pediatric team, working closely with the three units’ Patient Care Directors and fellow Clinical Managers. The Epicenter of Pediatric Nursing in a World Class OrganizationClinical Nurse Manager - Pediatric Service Line Evening FlexAt NewYork-Presbyterian, amazing things are truly happening!

New!

Jersey City, NJ6 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.

NY30+ days ago

$66,518–$99,777 Per Year

What you will do: Partner with Clinical Operations Trial Managers and cross-functional teams to support the planning, coordination, and day-to-day execution of clinical trials across the study lifecycle, including but not limited to issue tracking, protocol deviation review, and study status reporting, to help ensure quality, timeliness, and achievement of study goals. Clinical Trial Associate level is expected to be between $82,022 and $123,033 annualized and the current base salary range for this position at the Clinical Trial Associate level is expected to be between $66,518 and $99,777; final salary will be determined based on various factors including, but not limited to, years of relevant experience, job knowledge, skills and proficiency, degree/education, and internal comparators.

NY30+ days ago

$136,400–$181,400 Per Year

Lead and contribute to strategic initiatives and task forces aimed at improving clinical operations processes and outcomes, driving projects from inception to completion in alignment with organizational goals and in collaboration with cross-functional teams. General Description: The Senior Clinical Research Manager oversees clinical monitoring activities and the CRA team's performance to ensure they comply with ICH-GCP, local regulations, and company SOPs, and maintain quality across clinical trials.

Secaucus, NJ30+ days ago

Performs study procedures (e.g., obtain ECG recordings, vital signs, safety assessments, etc.) as required by study protocol under the supervision of the Clinical Research Coordinator, Principal Investigator, and Sub-Investigators. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Lake Success, NY17 days ago

Identifies and pursues extramural funding opportunities through pursuit of grants and clinical trials; collaborates with physicians, investigators and other healthcare providers regarding subject care as necessary; promotes respect for subjects' rights. When determining a team members base salary and/or rate, several factors may be considered as applicable (e.g., location, specialty, service line, years of relevant experience, education, credentials, negotiated contracts, budget and internal equity).

New York, NY13 days ago

$130,000–$150,000 Per Year

The CRM supervises clinical research coordinators, manages study operations across multiple trials, and collaborates with investigators, regulatory teams, research pharmacy, and clinical departments to ensure the successful implementation of complex cell and gene therapy clinical trials. Reporting to the CICET CGTM Senior Research Nurse Manager, the CRM leads the coordination and execution of investigator-initiated and industry-sponsored clinical trials, ensuring compliance with Good Clinical Practice (GCP), FDA regulations, institutional policies, and sponsor requirements.

New York City, NY12 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.

Manhasset, NY30+ days ago

This role will be responsible for combining concierge-level service with strategic process improvement, understanding and communicating complex processes, developing and maintaining resources, providing high levels of customer service, and ensuring smooth communication across departments. Partners with management to implement project initiatives; partners with management to design staff education programs and coordinates implementation, participates in educational initiatives, as needed; monitors project plan performance and prepares status reports.

Bronx, NY8 days ago

$84,000–$105,000 Per Year

The Clinical Research Program Manager- Monitor will be responsible for all ongoing monitoring activities -patient case reviews, pharmacy reviews, regulatory reviews for Montefiore Einstein Cancer Center Investigator Initiated Trials (trials where MECC clinicians are the Sponsor Investigators/IND Holder). Demonstrated communication, leadership, and team building skills: evidence of this should include dealing well with people, effective problem solving, appropriately confronting issues, motivating others as individuals and as groups, planning, organizing and directing the activities of others.

NY22 days ago

$87,400–$109,250 Per Year

Below is a summary of salary ranges for this role in the following geographies: California, New York State and Washington State Base Compensation Ranges: $87,400 - $109,250, Colorado Base Compensation Ranges: $83,600 - $104,500. Today''s healthcare system poorly serves chronic conditions that require ongoing support outside of the exam room, like obesity, diabetes, hypertension, cholesterol, and musculoskeletal conditions.

NY30+ days ago

$133,900–$200,900 Per Year

Responsibilities are focused on the management and career development of the organization's Clinical Research Associate (CRA) workforce and, if applicable, GCM Managers located in a region/area as well as supporting the development of departmental initiatives to strengthen the quality and productivity of GCM operations. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.

Clifton, NJ30+ days ago

Lead patient recruitment activities, e.g., performing chart reviews, discussing protocols with patients, and verifying the informed consent documentation to meet enrollment targets on assigned studies, with accountability for achieving enrollment goals. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

NY30+ days ago

$121,800–$182,600 Per Year

Skills: Competencies: Demonstrates mastery knowledge of ICH-GCP, applicable local regulatory requirements, relevant Precision for Medicine SOPs, technical CRA knowledge of all phases of study (including remote monitoring and clinical data review) as well as regulatory guidance. This compensation range takes into account the wide range of factors that are considered in making compensation decisions including but not limited to: skill sets, experience and training, licensure and certifications, and other business and organizational needs.

NY29 days ago

$91,500–$137,300 Per Year

Essential functions of the job include but are not limited to: Oversees all aspects of study site management to ensure patient safety is protected, quality of data generated by managed sites resulting in consistently low query levels and in acceptable Quality Assurance reports. Documents activities via confirmation letters, follow-up letters, trip reports, communication logs, and other required project documents as per SOPs, Clinical Monitoring Plan/Site Management Plan and client requirements.

NY30+ days ago

Remote

$90,000–$100,000 Per Year

What We are Looking for: Bachelor's degree, RN, or equivalent combination of education and relevant experience; life sciences background preferred 3+ years of clinical monitoring experience within sponsor, CRO, or investigative site environments Hands-on oncology monitoring experience required, including Phase I studies Strong knowledge of ICH-GCP guidelines and applicable regulatory requirements Ability and willingness to travel up to 30% based on study needs Excellent organizational skills with strong attention to detail Strong communication skills and ability to manage site relationships effectively Experience using CTMS, EDC, eTMF, and other clinical trial systems Experience in early-phase startup environments Ability to independently prioritize workload across multiple sites and studies Why Pharmaron? Position: Clinical Research Associate II, Oncology Location: Remote (East Coast USA Preferred) Salary: $90,000 to $100,000 D.O.E Unfortunately, we cannot support work visa permit applications for this role About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life.

Parsippany, Kansas30+ days ago

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

New York, NY30+ days ago

$75,000–$85,000 Per Year

You will own core transactional AR workflows, including monitoring sponsor and site-level accounts, supporting timely collections, posting cash in RealTime CTMS, and assisting with invoicing as needed. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

New York, NY30+ days ago

$85,000–$105,000 Per Year

New York, NY10 days ago

$85,000–$105,000 Per Year

Through the Iterative Health Site Network - a premier network of 100+ clinical research sites across the US and Europe - we help expand and expedite access to novel therapeutics for patients in need. By combining deep expertise in clinical trials with cutting-edge AI, we empower research teams and study sponsors to expand and expedite access to novel therapeutics for patients in need.

Mahwah, NJ18 days ago

Leading people who perform project management duties involving cross-functional teams focused on delivering internal products or administrative systems. Organizing project activities and interdepartmental meetings, ensuring communication facilitates the completion of the program or project on schedule and within budget constraints.

NY16 days ago

Remote

$110,000–$140,000 Per Year

Keywords: Phase One Oncology CRA, Clinical Research Associate, Phase I Oncology, First-in-Human Trials, Dose Escalation, Oncology Clinical Research, GCP, FDA Regulations, Clinical Monitoring, Biotechnology, Pharmaceutical. Piper Companies is seeking a Phase I Oncology Clinical Research Associate to support early-phase oncology clinical trials within the biotechnology and pharmaceutical industry.

NY30+ days ago

Remote

$155,000–$175,000 Per Year

Keywords: clinical research, clinical trials, CRA, general medicine, GCP, ICH, regulatory compliance, site monitoring, CTMS, EDC, protocol training, clinical documentation, data review, query resolution, clinical operations, FDA regulations, SOPs, quality oversight, risk-based monitoring, therapeutic areas. The Senior Clinical Research Associate (CRA) will join a remote, contract-based team supporting Phase II and Phase III studies across a variety of general medicine indications within a full-service clinical research environment.

NY10 days ago

Remote

$97,000–$193,000 Per Year

Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.

Hackensack, NJ30+ days ago

Hackensack Meridian Health nurses care for patients and their families at every stage of life, 24 hours a day, at bedsides in 9 community hospitals, 4 academic medical centers, a behavioral health hospital, 2 children's hospitals, 2 rehabilitation hospitals, medical offices, and care facilities across the state. 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.

Parsippany, New Mexico30+ days ago

As a CRC, you will play a critical role in coordinating study operations, supporting patient recruitment and retention, performing study‑related procedures, and ensuring adherence to study protocols and regulatory requirements. This role is well‑suited for a detail‑oriented research professional who enjoys direct patient interaction, values data integrity, and is committed to high‑quality clinical research within diverse communities.

New York, NY30+ days ago

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 Rockefeller University Clinical Research Center (RCRC) will be a state-of-the-art facility that will provide high-quality patient care and conduct innovative research in the field of clinical trials.

New York City, NY7 days ago

$112,154.40–$168,231.60 Per Year

In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). The CRA is responsible for the preparation, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with AZ Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the.

Parsippany, Kansas11 days ago

The CRC will play a critical role in study coordination, patient engagement, clinical procedures, and data management while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

New York, NY30+ days ago

$69,500–$72,500 Per Year

The Clinical Research Coordinator I is an intermediate level position that provides independent study coordination for simple and moderately complex clinical research studies such as registries, retrospective data reviews, studies in long-term follow-up, and other non-interventional studies or under supervision provides study coordination for moderate complexity to high complexity clinical trials with supervision such as such as EFS and pivotal IDE/IND studies. Decision Making/Autonomy: Carries out research projects per guidelines and regulation with limited supervision, collaborating both independently and with the Principal Investigator (PI) and Clinical Research Manager.

Secaucus, NJ30+ days ago

$20–$22 Per Hour

Our core competencies include pre-clinical, drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking a proactive and detail-oriented Clinical Research Assistant to provide critical administrative and operational support within our research environment.

New York City, NY12 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, NY12 days ago

$19–$44 Per Hour

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.

Newark, NJ30+ days ago

Aligned with Rutgers UniversityNew Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and five centers and institutes that focus on cancer treatment and research, neuroscience, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research. Under Policy 100.3.1 Immunization Policy for Covered Individuals, if employment will commence during Flu Season, Rutgers University may require certain prospective employees to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless the University has granted the individual a medical or religious exemption.

Hackensack, New Jersey17 days ago

Ensures timely, accurate, and reliable documentation, tracking, and reporting of all required clinical trial study and patient data and metrics through routine collaboration with all research team members including but not limited to Investigators, Clinical Research Nurses, Clinical Research Coordinators, Regulatory and Study Start-Up Specialists, Clinical Data Coordinators, Study Contract and Finance Staff, Sponsors and Contract Research Organizations, and other team members throughout the HMH Network as required. Focuses on continuous process improvement strategies both within the assigned Research Program or Division and throughout the entire HMH Research Enterprise, always seeking opportunities for streamlining and/or accelerating accruals to clinical trials, data cleaning, data quality, and trial completion.

New York, NY30+ days ago

$67,000–$69,000 Per Year

The CRC will have strong organizational, multi-tasking, time management, communication, and interpersonal skills to join the Anesthesiology Department's C3Are Team (Columbia Critical Care Anesthesiology Research) in executing clinical trials for improving treatments and outcomes for patients in the Intensive Care Units. The main role of the CRC will be to operate and maintain the day-to-day (night & weekends included) operational duties of their assigned clinical trials and clinical research study database.

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Clinical Jobs in Woodhaven, NY

Vice President Clinical Development Ophthalmology Jobot

Sr. Oncology Clinical Research Associate Jobot

Hospice Clinical Coordinator RN (Inpatient Hospice) Jobot

Licensed Clinical Social Worker BMS Family Health and Wellness Centers

Clinical Solutions Manager- Informatics Medline Industries

Associate Director, Clinical Development Trial Lead (CDTL) Joulé

Executive Medical Director, Clinical Development - M.D. (Nephrology) Clinical Dynamix, Inc.

Clinical Nurse Manager - 2RW - Night Flex NewYork-Presbyterian

RN Clinical Reviewer Greenlife Healthcare Staffing

Clinical Nurse Manager - RN – Perioperative Services – Full-time - Days (7AM-5PM) NewYork-Presbyterian

Clinical Nurse Manager - RN – ED – FT Nights NewYork-Presbyterian

Clinical Nurse Manager - Pediatric Oncology Center HIP7 - Morgan Stanley Children's Hospital NewYork-Presbyterian

Clinical Nurse Manager - Cardiac Med Telemetry SDU - Full Time Evenings NewYork-Presbyterian

Clinical Nurse Manager - Pediatric Service Line Evening Flex NewYork-Presbyterian

Urogynecologist Hackensack Meridian Health

Clinical Trial Associate/Sr. Clinical Trial Associate, Clinical Operations Agios Pharmaceuticals Inc

Senior Clinical Research Manager BeOne Medicines AG

Assistant Clinical Research Coordinator/Equipment Supervisor Frontage Clinical Services Inc

Clinical Research Program Manager Northwell Health Inc

Senior Clinical Research Manager - CICET Columbia University

Clinical Research Coordinator III Adams Clinical

Senior Project Manager - Clinical Research Northwell Health Inc

Program Manager Clinical Research Montefiore Medical Center

Clinical Research Coordinator Omada Health Inc

Senior Manager, Global Clinical Monitoring Precision Medicine Group LLC

Clinical Research Coordinator II Iterative Scopes Inc

Manager, Global Clinical Monitoring Precision Medicine Group LLC

Clinical Research Associate II - FSP Precision Medicine Group LLC

Clinical Research Associate II, Oncology Pharmaron Beijing Co Ltd

Clinical Research Associate - Sponsor Dedicated IQVIA

Clinical Research Finance Specialist Iterative Scopes Inc

Senior Clinical Research Finance Specialist Iterative Scopes Inc

Sr. Clinical Research Specialist - Site Ops Iterative Scopes Inc

Clinical Research Project Manager iMPact Business Group

Phase I Oncology Clinical Research Associate Zp Group Llc

Senior Clinical Research Associate Zp Group Llc

Senior Clinical Research Associate - CNS/Psychiatry - East Coast - Remote Worldwide Clinical Trials Holdings Inc

Clinical Research Nurse - Phase 1 - F/T - Days Hackensack University Medical Center

Clinical Research Coordinator - Albuquerque, NM IQVIA

Clinical Research Nurse | Diagnostic & Treatment Center (*4 positions available) Rockefeller University

Clinical Research Associate - New York / New Jersey AstraZeneca Plc

Clinical Research Coordinator - Wichita, KS IQVIA

Clinical Research Coordinator I - Cardiology (CARE) Columbia University

Clinical Research Administrative Assistant Frontage Clinical Services Inc

Clinical Research Assistant, PRN Care Access

Clinical Research Assistant, PRN (Phlebotomist, LVN or Registered Nurse) Care Access

Clinical Research Nurse | Diagnostic & Treatment Center Rockefeller University

Clinical Research Coordinator II Rutgers The State University of New Jersey

Project Manager, Clinical Trials Hackensack Meridian Health

Clinical Research Coord I Columbia University

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