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architectural lighting project manager (procurement) Jobs in New York

project coordinator

Columbia University

<div><ul><li>Job Type: Officer of Administration</li>
<li>Bargaining Unit:</li>
<li>Regular/Temporary: Regular</li>
<li>End Date if Temporary:</li>
<li>Hours Per Week: 35</li>
<li>Standard Work Schedule:</li>
<li>Building:</li>
<li>Salary Range: 67,000-70,000</li>
</ul><div><i>The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.</i></div><br>
<div></div>
<p></p>
<p>Position Summary</p>
<p>
The School of Nursing is looking to hire a Research Coordinator to work with Center for Research on People of Color (CRPC). The incumbent will work closely with the Executive Director, Project Director, and Project Manager to assist in various day-to-day operations and study related tasks.</p>
<p></p>
<p>Responsibilities</p>
<p>
Responsibilities will include:</p>
<ul>
<li>Coordinate research study tasks, including subject recruitment, participant scheduling, preparation of study materials, participant enrollment, data collection and data entry.</li>
<li>Coordinate Live Music meetings, set agenda items, take meeting minutes, and assist with communication across study</li>
<li>Assist in tracking project progress and reporting updates to study teams.</li>
<li>Attend staff and study team meetings.</li>
<li>Communicate clearly and routinely with study team.</li>
<li>Support Project Director with building/maintaining relationships with community partners.</li>
<li>Assist with research and manuscript preparation for publication and dissemination of results.</li>
<li>Assist coordination of CRPC social media presence (LinkedIn and Facebook).</li>
<li>Organize and support event planning for CRPC and related research studies.</li>
<li>Support Project Director with study IRB (i.e. assist with modifications as needed and process revisions and annual continuation process for Institutional Review Board (IRB) submissions)</li>
<li>Assist with other research study and CRPC tasks as needed.</li>
<li>Position requires travel to participants throughout NYC.</li>
<li>Position may require occasional evening and weekend hours.</li>
</ul>
<p>The continuation of this role is contingent upon future grant-funding and/or funding for the Center for the Research on People of Color.</p>
<p></p>
<p>Minimum Qualifications</p>
<ul>
<li>Bachelor&rsquo;s degree or equivalent in education and experience, plus three years of related experience.</li>
<li>Experience in health related research.</li>
<li>Computer fluency with Microsoft Suite.</li>
<li>Excellent verbal and written communication</li>
<li>Excellent interpersonal and organizational skills.</li>
<li>Ability to work well in a team.</li>
<li>Attention to detail.</li>
<li>Must be a highly motivated, self-starter.</li>
</ul>
<p></p><p>Preferred Qualifications</p>
<ul>
<li>Master&rsquo;s degree:
<ul><li>A major in public health, psychology, nursing or related field.</li>
</ul></li><li>Experience or interest in working with the community</li>
</ul>
<p></p><p>Equal Opportunity Employer / Disability / Veteran</p>
<p>
Columbia University is committed to the hiring of qualified local residents.</p></div>

Research Coordinator

Artcreativity

<p><b>What You&rsquo;ll Do</b></p><p>This is a hybrid support role combining Amazon claims, project coordination, and operations support for our Ordering, Shipping &amp; Compliance Team. You&rsquo;ll work closely with the department Head to keep projects moving and ensure issues are resolved quickly.</p><p><b>Key responsibilities include:</b></p><ul><li>Proactively pursue and assist with Amazon cases and claims (lost, damaged, or missing inventory, shipments, listings, etc.) and track case progress</li><li>Follow up on open cases in Amazon Seller Central</li><li>Assist Project Coordinator with overseas suppliers to support ongoing projects when needed</li><li>Track timelines and ensure deadlines are met</li><li>Upload and manage product documentation, testing reports, and certifications</li><li>Support shipping and logistics coordination</li><li>Maintain organized spreadsheets and internal records</li><li>Handle day-to-day follow-ups and administrative tasks for the team, especially in regard to Amazon cases, Amazon SAS cases, and phone calls to Amazon.</li></ul><p><b>What We&rsquo;re Looking For</b></p><ul><li>Highly organized with strong attention to detail</li><li>Comfortable managing multiple tasks and priorities</li><li>Strong written and verbal communication skills</li><li>Proficient in Excel or Google Sheets</li><li>Self-motivated and reliable</li></ul><p><b>Nice to have (not required):</b></p><ul><li>Exposure to Amazon Seller Central or e-commerce</li><li>Experience in admin, logistics, or coordination roles</li></ul><p>Pay: From $20.00 per hour</p><p>Benefits:</p><ul><li>Paid time off</li></ul><p>Work Location: In person</p>

Claims & Project Support Specialist

Milan Restoration

<p><b>About Us</b></p><p>Milan Restoration is a family‑owned architectural conservation firm preserving historic buildings, monuments, and culturally significant structures. Since 1987, we&rsquo;ve partnered with architects, engineers, cultural institutions, and government agencies to restore historic fabric with precision and European craftsmanship.</p><p>We are looking for an Administrative Assistant who is detail‑oriented, organized, and motivated to support meaningful work in historic preservation.</p><p><b>Position Summary</b></p><p>The Administrative Assistant provides administrative, operational, and project support to leadership. This role supports active conservation projects, prepares documentation, manages submittals, and helps keep project workflows organized.</p><p>This position begins with a 4-6 week paid temp-to-hire period. If the partnership aligns well in communication, work, quality, and shared values, we look forward to discussing a transition into a full‑time, permanent position.</p><p><b>Key Responsibilities</b></p><p><b>Administrative Support</b></p><ul><li>Draft correspondence for architects, clergy, preservation boards, cultural institutions, and governmental agencies</li><li>Prepare presentations, proposals, and reports that reflect Milan Restoration's craftsmanship and conservation philosophy</li><li>Assist with scheduling, document formatting, and general office tasks</li></ul><p><b>Project Support</b></p><ul><li>Assist with investigative reports, condition assessments, scopes of work, submittals, and change orders</li><li>Organize project photography, drawings, and historical documentation</li><li>Manage submittal logs, track submittal status, and ensure timely distribution to architects, engineers, and project stakeholders</li><li>Track project milestones across disciplines (masonry, stained‑glass, plaster, stone carving, and historic finishes)</li></ul><p><b>Office &amp; Operations Support</b></p><ul><li>Maintain organized digital and physical archives of drawings, lab reports, historical documents, and project photography</li><li>Support invoice processing, expense tracking, and financial documentation</li><li>Assist with onboarding new conservators, artisans, and field staff</li><li>Perform additional duties as assigned</li></ul><p><b>Required Qualifications </b></p><ul><li>1&ndash;2 years as an Administrative Assistant, Project Coordinator, or similar role</li><li>High School diploma or equivalent required; college degree preferred</li><li>Experience in construction, architecture, historic preservation, or a related technical field</li><li>Strong attention to detail and accuracy</li><li>Self-motivated and proactive in problem-solving and follow-up</li><li>Proficient in Microsoft Office, Excel, and general office software; familiarity with ProCore or similar platforms</li><li>Professional communication skills (written and verbal)</li><li>Ability to work Monday-Friday, 9 AM - 5 PM in a hybrid schedule (New York, NY)</li><li>Comfortable with a 4-6 week temp-to-hire period</li></ul><p><b>Preferred Qualifications</b></p><ul><li>Experience preparing or managing submittals</li></ul><p><b>How to Apply</b></p><p>Please submit your resume and answer the Indeed screening questions.</p><p>We will ask about:</p><ul><li>Your experience with submittals</li><li>Your administrative/project support background</li><li>Your fit for Milan Restoration's mission and work environment</li></ul><p>Pay: $24.00 - $26.00 per hour</p><p>Benefits:</p><ul><li>Flexible schedule</li></ul><p>Application Question(s):</p><ul><li>In a brief summary, please explain why you believe you&rsquo;re a strong fit for Milan Restoration&rsquo;s work environment and mission. In your message, please also share any experience you have preparing or managing submittals, project logs, or similar documentation. </li></ul><p>Work Location: Hybrid remote in New York, NY 10013</p>

Administrative Assistant (Hybrid) Temp-to-Hire

Orthodox Union

<div><div><b>Who We Are:
</b></div><div>The Orthodox Union (OU) is one of the largest Orthodox Jewish organizations in the United States. Founded in 1898, the OU supports a network of synagogues, youth programs, Jewish and Religious Zionist advocacy programs, programs for the disabled, localized religious study programs, and international units. The OU maintains a kosher certification service, whose circled U symbol, Ⓤ, is found on the labels of many kosher commercial and consumer food products.</div><p></p><div><b><br>
Position Summary:
</b></div><p>The Creative Coordinator plays a key role in supporting the execution of creative and marketing projects across the OU. This role helps ensure projects are well-organized, clearly structured, and prepared for efficient execution.</p><div>
The ideal candidate is highly organized, detail-oriented, and comfortable managing multiple workstreams at once. This role is best suited for someone early in their career who is ready to take on responsibility in preparing assets, supporting workflows, and contributing to the creation of marketing materials within established guidelines.</div><p></p><div><b><br>
Responsibilities:</b></div><ul><li>
Support the creation of marketing materials, including producing basic flyers, simple layouts, and website graphics (e.g., thumbnails, headers) using established templates and brand guidelines</li><li>
Prepare and format visual assets for use across digital and print projects, including resizing images and making light edits as needed</li><li>
Ensure projects are execution-ready by gathering missing inputs, organizing materials, and maintaining clarity around deliverables</li><li>
Prepare and organize files for use across projects, ensuring accuracy, consistency, and proper formatting</li><li>
Support the organization and maintenance of creative assets and file systems to ensure easy access and proper versioning</li><li>
Work closely with the Project Manager and creative team to support project execution, including following up on assets and internal inputs as needed</li><li>
Assist in organizing project materials and assets once projects are in motion</li><li>
Conduct basic research and assist with internal tracking and reporting as needed</li><li>
Manage communication with external designers and copywriters to uphold brand standards, provide actionable feedback, and ensure final deliverables align with expectations</li></ul><p></p><div><b><br>
Qualifications</b><b>:</b></div><ul><li>
BA/BS required or comparable experience</li><li>
1&ndash;2 years of relevant experience (internships included) in a creative, marketing, or related environment</li><li>
Highly organized with strong attention to detail and the ability to manage multiple tasks simultaneously</li><li>
Comfortable working in a fast-paced environment with shifting priorities</li><li>
Strong communication skills, both written and verbal</li><li>
Ability to work collaboratively and follow through on assignments</li><li>
Familiarity with design tools (e.g., Canva, Adobe Photoshop, or InDesign) for basic asset creation and editing is a plus</li><li>
Experience with Monday.com or similar project management tools is a plus</li></ul><div></div><div><b><br>
Salary &amp; Benefits:</b></div><div>
The salary range for this position is<b> </b><b>$5</b><b>0</b><b>,000 - $6</b><b>0</b><b>,000</b>, commensurate with experience.</div><div></div><div><b><br>
Health, Dental &amp; Vision Insurance:</b><br>
The OU offers health insurance through an Individual Coverage Health Reimbursement Arrangement (ICHRA). Instead of a single group plan, employees have the freedom to choose their own health insurance plan that fits their personal and family needs. The OU contributes a generous monthly amount directly toward your premium, making coverage more flexible, affordable, and tailored to you.</div><div></div><div><br>
Employees enrolled in our health plan also receive an annual BeniComp stipend, a supplemental benefit that reimburses eligible medical, pharmaceutical, dental, and vision expenses.</div><div></div><div><br>
In addition, the OU offers employees group dental and vision insurance through MetLife.</div><div></div><div><b><br>
Additional Benefits and Perks:</b></div><ul><li>
10 Paid sick days</li><li>
10 Paid vacation days</li><li>
Paid Jewish and Federal holidays</li><li>
Short Fridays to accommodate for Sabbath observance</li><li>
Free life and disability insurance</li><li>
Discounted continuing education opportunities</li><li>
403(b) retirement plan with a 5% employer match after 3 years (requires a minimum 2% employee contribution)</li></ul></div><p></p>

Creative Coordinator

NYU Langone Health

<div><p>NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge.
<br>
<br>
<i>For more information, go to</i> <i>med.nyu.edu</i>, and interact with us on <i>LinkedIn</i>, <i>Glassdoor</i>, <i>Indeed</i>, <i>Facebook</i>, <i>Twitter</i> <i>and</i> <i>Instagram</i>.</p>
<p><b>
Position Summary:</b></p><p><br>
We have an exciting opportunity to join our team as a Research Coordinator.
<br>
<br>
The Section of Digitally Enabled Care (SoDEC) at NYU Grossman School of Medicine is hiring a Research Coordinator to assist with day-to-day research activities including research design, study management, data collection, preliminary data analysis, and dissemination of results. Responsibilities include coordinating study operations in accordance with approved protocols; preparing and submitting regulatory materials to the Institutional Review Board (IRB); and supporting manuscript and abstract development. The Research Coordinator will work as part of a team to initiate, conduct, and manage recruitment for research studies, including working closely with providers and clinical staff, coordinating outreach activities, and managing study documentation. The successful candidate will demonstrate a high degree of professional maturity, commitment to excellence, independence, flexibility, and initiative, and will possess the ability to work collaboratively with diverse individuals, teams, and populations both internally and externally.<br>
The position will be based in the Division of Healthcare Delivery Sciences Section of Digitally Enabled Care in the Department of Population Health, a dynamic learning environment focused on improving patient safety and outcomes.[</p>
<p><b>
Job Responsibilities:</b></p>
<ul>
<li>Collaborate with internal and external research team members to plan, coordinate, and monitor research activities in support of study objectives.</li>
<li>Support day-to-day operations of research studies, including study management, documentation, and coordination of project activities.</li>
<li>Ensure accurate execution of research protocols in accordance with HIPAA regulations and institutional policies.</li>
<li>Assist with regulatory activities, including preparation and submission of documents to the NYU Institutional Review Board (IRB) and maintenance of regulatory files.</li>
<li>Support recruitment, screening, and enrollment of study participants.</li>
<li>Collect and manage research data from electronic health records (EHR) and other sources.</li>
<li>Assist with data analysis, interpretation of findings, and preparation of reports, presentations, and other study deliverables.</li>
<li>Conduct literature reviews and assist with preparation, editing, and submission of manuscripts, abstracts, and presentations for dissemination.</li>
<li>Coordinate research team meetings, prepare agendas and minutes, and facilitate communication among investigators, clinical staff, and external collaborators.</li>
<li>Assist with grant-related activities, including preparation of materials for grant applications and required progress reports.</li>
<li>Perform other duties as assigned in support of research and departmental priorities.</li></ul><br>
<p></p>
<p><b>
Additional Position Specific Responsibilities:</b><br>
Familiarity with health services and population health research.<br>
Bonus: experience with EHR clinical data, chart review, and/or qualitative research.</p>
<p><b>
Minimum Qualifications:</b><br>
To qualify you must have a Bachelor's degree in life sciences, allied health or equivalent in a related discipline and 0-1 years experience or an equivalent combination of education and experience. Effective oral, written, communication, interpersonal skills. Must be able to work under the direction of supervision. Ability to operate research related equipment. Proficiency in using various Microsoft Office applications such as World, Excel, Access, Power Point and Outlook. Familiar with Internet applications. Ability to identify, analyze and solve problems. Time management skills and ability to work well under pressure.</p>
<p><b>
Preferred Qualifications:</b><br>
Knowledge of basic medical terminology is preferred. Prior experience working with Research Protocols. Experience working in an academic medical center environment</p>
<p><i>
Qualified candidates must be able to effectively communicate with all levels of the organization.</i>
<br>
<br>
NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents. At NYU Langone Health, we are committed to supporting our workforce and their loved ones with a comprehensive benefits and wellness package. Our offerings provide a robust support system for any stage of life, whether it's developing your career, starting a family, or saving for retirement. The support employees receive goes beyond a standard benefit offering, where employees have access to financial security benefits, a generous time-off program and employee resources groups for peer support. Additionally, all employees have access to our holistic employee wellness program, which focuses on seven key areas of well-being: physical, mental, nutritional, sleep, social, financial, and preventive care. The benefits and wellness package is designed to allow you to focus on what truly matters. Join us and experience the extensive resources and services designed to enhance your overall quality of life for you and your family.
<br>
<br>
NYU Grossman School of Medicine is an equal opportunity employer and committed to inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration. We require applications to be completed online.
<br>
<br>
View Know Your Rights: Workplace discrimination is illegal.</p>
<p>
NYU Langone Health provides a salary range to comply with the New York state Law on Salary Transparency in Job Advertisements. The salary range for the role is $66,299.99 - $66,300.00 Annually. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range or contractual rate listed does not include bonuses/incentive, differential pay or other forms of compensation or benefits.</p>
<p>
To view the Pay Transparency Notice, please click here</p></div>

<div><ul><li>Job Type: Officer of Administration</li>
<li>Bargaining Unit:</li>
<li>Regular/Temporary: Regular</li>
<li>End Date if Temporary:</li>
<li>Hours Per Week: 35</li>
<li>Standard Work Schedule:</li>
<li>Building:</li>
<li>Salary Range: $66,300-$68,000</li>
</ul><div><i>The salary of the finalist selected for this role will be set based on a variety of factors, including but not limited to departmental budgets, qualifications, experience, education, licenses, specialty, and training. The above hiring range represents the University's good faith and reasonable estimate of the range of possible compensation at the time of posting.</i></div><br>
<div></div>
<p></p>
<p>Position Summary</p>
<div>
<p>The Clinical Research Coordinator manages clinical trials conducted through the Clinical Protocol &amp; Data Management Office. This position reports directly to the Clinical Research Manager of the specific disease site this incumbent is assigned to. Subject to business needs, we may support flexible and hybrid work arrangements. Options will be discussed during the interview process.</p>
</div>
<p></p><p>Responsibilities</p>
<p>
The Clinical Research Coordinator manages clinical trials (including some regulatory and budget requirements) and assists in the coordination of tests/visits for patients, working with the study team to maximize work efficiency to gather all required data and relevant clinical information.</p>
<p>
Responsibilities include, but are not limited to:</p>
<ul>
<li><b>GENERAL STUDY MANAGEMENT</b>
<ul><li>Reviewing research protocols.</li>
<li>Assisting Principal Investigators in study start up and submitting studies to appropriate offices.</li>
<li>Interacting with the regulatory team to maintain regulatory documentation and administrative files for each protocol</li>
<li>Under the supervision of the clinical research manager, the coordinator maintains procedures necessary for timely and complete data management, and complies with required supervision tools such as work logs and regular meetings. The coordinator will also comply with necessary regulatory responsibilities as needed.</li>
</ul></li></ul><ul><li><b>PATIENT MANAGEMENT</b><br>
<ul><li>Coordinates study enrollment, protocol treatment, and follow-up care for patients participating in clinical trials in conjunction with the clinical research nurse, research pharmacy, treatment center and other study staff.</li>
<li>Working with the research nurse, treating physicians, and Principal Investigators to confirm that each patient meets eligibility criteria specified for protocols and enrollment into clinical trials.</li>
<li>Communicating with various departments, physicians, labs, outside hospitals, and all members of the clinical team to ensure accuracy, timely retrieval of data, and confirm the appropriateness and timeliness of tests.</li>
<li>Collecting follow-up data on patients' post-treatment as required by the protocol and submit monthly reports to the clinical protocol office, tracking patient enrollment and accounts/payments for sponsored protocols.</li>
<li>Completes timely research billing review</li>
<li>Maintains and updates sponsor-related, university and department databases/logs</li>
</ul></li></ul><ul><li><b>DATA MANAGEMENT</b>
<ul><li>Handling data management requirements for each patient enrolled.</li>
<li>Abstracts, assembles, and organizes clinical research data.</li>
</ul></li></ul><ul><li><b>OTHER</b>
<ul><li>Coordinator performs other related duties and participates in special projects as assigned.</li>
<li>Perform other related duties and responsibilities as assigned/requested.</li>
</ul>
</li></ul><p></p><p>Minimum Qualifications</p>
<ul>
<li>Bachelor&rsquo;s degree or equivalent in education and/or experience.</li>
</ul>
<p></p><p>Preferred Qualifications</p>
<ul>
<li>Two years of related experience or equivalent in education.</li>
<li>Excellent interpersonal and organizational skills.</li>
<li>Computer Skills: proficiency with MS Word programs and familiarity with Mac and PC platforms.</li>
<li>Experience in clinical research setting with knowledge of HIPAA and GCP.</li>
</ul>
<p></p><p>Equal Opportunity Employer / Disability / Veteran</p>
<p>
Columbia University is committed to the hiring of qualified local residents.</p></div>

Clinical Research Coordinator I

IQVIA

<div>New York, United States of America | Part time | Office-based | R1543649</div>
<br><div><div><h3 class="jobSectionHeader"><b>Clinical Research Coordinator - New York, NY</b><br>
<b>Work Set‑Up:</b><b> On‑site</b><br>
<b>Schedule:</b><b> Part‑time | 24 hours per week</b></h3><div><b>
About IQVIA</b></div><div>
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate clinical development and improve patient outcomes. By combining deep scientific expertise with innovative technologies, we deliver high‑quality data and insights that shape the future of healthcare.</div><div><b>
About the Role</b></div><div>
IQVIA is seeking a <b>highly experienced Clinical Research Coordinator (CRC)</b> to support the conduct of clinical research studies under the direction of a Principal Investigator. This role is hands‑on and patient‑facing, requiring strong clinical research expertise, the ability to manage multiple protocols, and a commitment to patient safety, regulatory compliance, and data integrity.</div><div>
The ideal candidate brings demonstrated experience leading study activities, coordinating visits, and supporting regulatory requirements in a fast‑paced clinical research environment.</div><div><b>
Key Responsibilities</b></div><ul><li><div>
Conduct clinical research visits and procedures, including ECGs, vital signs, and biological sample collection</div></li><li><div>
Coordinate day‑to‑day execution of multiple clinical research protocols simultaneously</div></li><li><div>
Ensure strict adherence to study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements</div></li><li><div>
Prepare study materials, organize equipment, and manage logistical planning for study visits</div></li><li><div>
Recruit, screen, consent, and orient study participants while ensuring safety and ethical conduct</div></li><li><div>
Accurately document clinical data in case report forms (CRFs) and electronic data capture (EDC) systems</div></li><li><div>
Collaborate with investigators, monitors, and sponsors to resolve queries and maintain data quality</div></li><li><div>
Provide regulatory support, including maintenance of essential documents and audit readiness</div></li><li><div>
Serve as a patient advocate and maintain a safe clinical environment in accordance with Health &amp; Safety policies</div></li></ul><div><b>
Required Qualifications</b></div><ul><li><div>
Bachelor&rsquo;s degree preferred or an equivalent combination of education and relevant experience</div></li><li><div><b>
Significant experience as a Clinical Research Coordinator, including prior responsibility as a Lead CRC managing multiple protocols concurrently</b></div></li><li><div><b>
Demonstrated experience conducting study visits independently and providing regulatory support</b></div></li><li><div>
Minimum of 1+ years of clinical research experience (additional experience strongly preferred)</div></li><li><div>
Strong working knowledge of clinical trial operations, GCP, and medical terminology</div></li><li><div>
Proficiency in EDC systems, data entry, and query resolution</div></li><li><div>
High attention to detail with the ability to build effective working relationships across cross‑functional teams</div></li><li><div>
Experience in <b>Neurology and/or Pediatrics is a plus</b>, but not required</div></li></ul><div><b>
Why Join IQVIA?</b></div><ul><li><div>
Be part of a globally recognized clinical research organization</div></li><li><div>
Work on meaningful studies that improve patient outcomes</div></li><li><div>
Collaborate with experienced investigators and research professionals</div></li><li><div>
Gain exposure to diverse protocols and therapeutic areas</div></li></ul><div><b><i>
Note: </i></b><i>This position is not eligible for sponsorship</i></div><div>
#LI-CES and #LI-DNP #LI-HCP #remote</div></div><div>
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com</div><div>
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe</div><div>
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.</div>
The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.</div>

Clinical Research Coordinator - New York, NY

Explore 420+ Project coordinator in New York this May. Find roles across top companies and apply now to boost your career.

420 project coordinator jobs In New York

Research Coordinator

Claims & Project Support Specialist

Administrative Assistant (Hybrid) Temp-to-Hire

Creative Coordinator

Research Coordinator

Clinical Research Coordinator I

Clinical Research Coordinator - New York, NY