160 Results for

Clinical Jobs in Riverhead, NY

Jobs

Clinical Research Coordinator U.S. Renal Care

Orange, CT

$65,000–$80,000

Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. (Including but not limited to: Form FDA 1572, financial disclosures, laboratory certifications, protocol, investigator brochure, institutional review board (IRB) related documents, IND reports delegation of authority (DOA), study specific enrollment logs, monitoring reports, with assistance as needed.

Today

Gynecologist, Clinical Assistant/Associate Professor, OBGYN, Minimally Invasive Gynecologic Surgery Stony Brook University SUNY

Stony Brook, NY

It encompasses Stony Brook University Hospital, Stony Brook Children's Hospital, the five Health Sciences schools -- Dental Medicine, Health Professions, Medicine, Nursing and Social Welfare -- as well as the major centers and institutes, programs and more than 50 community-based healthcare settings throughout Suffolk County. The Department of Obstetrics, Gynecology and Reproductive Medicine at Stony Brook Medicine is recruiting a full-time faculty member at the level of Assistant/Associate Professor to join a busy Minimally Invasive Gynecology academic practice with an established history of excellence.

Today

Global Women's Health Fellowship, Clinical Instructor, OBGYN Stony Brook University SUNY

Stony Brook, NY

It encompasses Stony Brook University Hospital, Stony Brook Children's Hospital, the five Health Sciences schools -- Dental Medicine, Health Professions, Medicine, Nursing and Social Welfare -- as well as the major centers and institutes, programs and more than 50 community-based healthcare settings throughout Suffolk County. Anticipated Start Date: July 2028 Campus Description Long Island's premier academic medical center, Stony Brook Medicine, represents Stony Brook University's entire medical enterprise and integrates all of Stony Brook's health-related initiatives: education, research and patient care.

Today

RN - Nursing Yale New Haven Health

Waterford, CT

Specific training and education for research studies will be provided as needed In personal and job-related decisions and actions, consistently demonstrates the values of integrity (doing the right thing), patient-centered (putting patients and families first), respect (valuing all people and embracing all differences), accountability (being responsible and taking action), and compassion (being empathetic). In personal and job-related decisions and actions, consistently demonstrates the values of integrity (doing the right thing), patient-centered (putting patients and families first), respect (valuing all people and embracing all differences), accountability (being responsible and taking action), and compassion (being empathetic).

30+ days ago

Senior Finance Manager, Clinical Research Yale University

New Haven, CT

Remote

$90,000–$165,750 / year

As a key member of the finance team, the Senior Finance Manager, Clinical Research must demonstrate the following competencies and characteristics: Proven strong leadership skills, including the ability to manage an organization and project teams effectively, both in terms of what they achieve and how they achieve it; Ability to build strong, trusting relationships with university stakeholders, while interacting effectively across all levels in multiple functional areas; Excellent interpersonal and communication skills. Enables academic leadership focus on program activities by: managing financial support services for the unit; assessing financial and/or operational challenges and opportunities and solving for and/or leveraging these working with the Director and/or others as appropriate; facilitating and strengthening the interface between unit needs/requirements and service providers and activities.

30+ days ago

YCCI Clinical Research Technical Trainer Yale University

New Haven, CT

$68,000–$120,500 / year

The Clinical Research Technical Trainer is a vital member of the Workforce Development and Training team, responsible for developing, delivering, and continuously improving training programs for clinical research professionals across the Yale School of Medicine (YSM), the Yale New Haven Hospital Delivery Network, and other schools across Yale. Develops and maintains an awareness of the Project Management disciplines essential to the on time, on budget delivery of complex IT Projects, including intricate work breakdown structure management and critical path analysis.

30+ days ago

Clinical Research Support Laboratory Manager Actalent Inc

New Haven, CT

$82,000–$131,500 / year

The position focuses on overseeing both wet and dry lab operations, managing laboratory resources and kit inventory, and ensuring laboratories can effectively support complex clinical trials, particularly in oncology. The Lab Manager oversees laboratory supervisors and operations across multiple locations in Connecticut, including sites such as Greenwich, North Haven, New Haven, and Trumbull, and will travel between these locations as needed.

3 days ago

Clinical Research Associate I Stony Brook University

Stony Brook, NY

Required Qualifications (as evidenced by an attached resume): Bachelor''s Degree (foreign equivalent or higher) and two (2) years of full-time related research experience in clinical trials research, research database management, and working with Institutional Review Board. Perform various administrative duties, which may include proper collection and shipment of lab samples; billing, budgeting and contract administration; maintenance of clinical research study supplies and drug accountability.

30+ days ago

Clinical Research Assistant Stony Brook University

Stony Brook, NY

Brief Description of Duties: The Clinical Research Assistant participates in enrolling human subjects into research protocols by performing informed consent process with potential study subjects, explaining protocols, answering questions, and fulfilling regulatory requirements for informed consent form; maintains consent forms; schedules visits, coordinates subject follow-up; in both the Infectious Diseases Clinic at Stony Brook University or research sites. In lieu of a Bachelor''s degree and One (1) year of full-time experience working in a patient-related research environment, an Associate's degree (foreign equivalent or higher) and Three (3) years of full-time experience working in a patient-related research environment may be considered.

30+ days ago

Director of Administration, Cancer Clinical Trials Office Stony Brook University

Stony Brook, NY

2600523'',''2600523'',''Senior Staff Associate'',''Senior Staff Associate'',''Administrative & Professional (non-Clinical)'',''Administrative & Professional (non-Clinical)'',''US-NY-Stony Brook'',''US-NY-Stony Brook'',''Cancer Center'',''Cancer Center'',''Full-time'',''Full-time'',''Day Shift'',''Day Shift'',''9 to 5'',''9 to 5'','''','''',''Jun 5, 2026'',''Jun 5, 2026'',''Jul 5, 2026, 10:59:00 PM'',''Jul 5, 2026, 10:59:00 PM'',''180,000 - $192,000'',''180,000 - $192,000'',''Regular'',''Regular'',''SL5'',''SL5'',''Stony Brook University'',''Stony Brook University'',''false'',''730383'',''730383'',''true'',''730383'',''false'',''Submission for the position: Director of Administration, Cancer Clinical Trials Office - (Job Number: 2600523)'',''false'',''730383'',''false'',''true''. ''730383'',''true'',''730383'',''false'',''Submission for the position: Director of Administration, Cancer Clinical Trials Office - (Job Number: 2600523)'',''false'',''730383'',''false'',''true'',''Director of Administration, Cancer Clinical Trials Office'',''!*!

30+ days ago

Director Of Administration, Cancer Clinical Trials Office Stony Brook University

Stony Brook, NY

Regulatory & Quality Assurance: Audit Readiness: Direct the internal Quality Assurance (QA) unit to conduct routine monitoring and audits; serve as the primary point of contact for external audits (NCI-CTEP, FDA, Sponsors). Personnel Management: Oversee the management of all CCTO staff (with mid-level leaders), ensuring optimal FTE levels, appropriate coverage for all units, and appropriate planning for future needs.

30+ days ago

Clinical Research Nurse 2 Yale University

New Haven, CT

$68,000–$120,500 / year

Main responsibilities will be: overseeing and implementation of the clinical research operation of the Testani laboratory, oversight and leadership of a team of study staff, maintenance of regulatory compliance for several ongoing heart failure studies in both hospitalized and ambulatory patients, and supervising and ensuring high fidelity collection and storage of data and biospecimens. Ability to assess protocols for feasibility and determine complexity, identify risks, logistics and challenges associated with operationalizing and implementing specific trials at Yale New Haven Hospital and other Yale New Haven Health locations.

30+ days ago

Cancer Clinical Trials Finance Manager Stony Brook University

Stony Brook, NY

$122,767–$145,656 / year

2602415'',''2602415'',''TH Staff Associate'',''TH Staff Associate'',''Finance'',''Finance'',''US-NY-Stony Brook'',''US-NY-Stony Brook'',''Clinical Trials'',''Clinical Trials'',''Full-time'',''Full-time'',''Day Shift'',''Day Shift'',''9:00 AM - 5:00 PM'',''9:00 AM - 5:00 PM'',''Sat, Sun'',''Sat, Sun'',''Jul 10, 2026'',''Jul 10, 2026'',''Oct 8, 2026, 11:59:00 PM'',''Oct 8, 2026, 11:59:00 PM'',''$126,767 - $149,656 / Total'',''$126,767 - $149,656 / Total'','''','''',''SL4'',''SL4'',''Stony Brook University Hospital'',''Stony Brook University Hospital'',''false'',''736623'',''736623'',''true'',''736623'',''false'',''Submission for the position: Cancer Clinical Trials Finance Manager - (Job Number: 2602415)'',''false'',''736623'',''false'',''true''. This means that when the Hospital is faced with an institutional emergency, employees in such positions may be required to remain at their work location or to report to work to protect, recover, and continue operations at Stony Brook Medicine, Stony Brook University Hospital and related facilities.

25 days ago

Senior Clinical Data Manager Celldex Therapeutics Inc

New Haven, CT

$133,579–$173,480 / year

Will work closely with internal team members and vendors to ensure that assigned clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals and expectations, and budget. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.

30+ days ago

Clinical Program Manager Integrated Resources, Inc

New Haven, Connecticut

Full time

Job Description• Leads the cross-functional execution of one or more clinical studies conducted within the Clinical Research Unit (CRU)• Accountable to CRU leadership and the Core Study Team for delivery of a CRU study according to agreed quality, timeline and cost parameters• Assures that CRU studies are conducted in compliance with GCP, relevant SOPs and local regulatory requirements• Assures data integrity and data quality for each assigned study through input to study feasibility and protocol development efforts, verification of EDCMS study set up, management of cross-study activities and coordination of CRU functional line data review/verification activities (e.g., data verification, data cache review, data listing reviews, study report reviews)• Coordinates and contributes to the assessment and minimization of operational risks and to the resolution of operational issues• Promotes best practices within and across CRU studies to drive operational excellenceResponsibilities-• Responsible for study/project management within the unit including study scheduling, protocol planning(start-up activity) and is the primary contact for the project teams responsible for the compound/project - from the time of the Study/project document is drafted until the data base/project is locked• Leads CRU cross-functional input to, and review of, the Study Protocol prior to finalization• Serves as primary liaison/point of contact for the Core Project Teams/Clinical Research Unit (CRU)• Develops and ensures adherence to study timelines• Coordinates and reviews all study activities• Serves as primary point of contact for on study decisions related to the protocol, data collection and volunteer activities• Partners with line leaders and functional staff across CRU departments• Maintains accuracy, accessibility and confidentiality of all volunteer records and reports o In depth review of all clinical data, serves as study monitor, ensures all data is complete and checked before database lock and release• Leads the data integrity/data quality activities for assigned protocols• Reviews Informed Consent Document for IRB submission• Provides critical assessment of strategic partner and vendor proposals to ensure study success• Reviews site level clinical trial budget• Leads other functions and strategic partners to ensure timely delivery of quality data• Oversees the overall execution of clinical studies• Participates in study meeting with relevant partners for operational alignment• Communicates opportunities and risks to the Core Project Teams for integration in risk management plans• Effectively coordinates all functional areas involved in clinical trials to solve problems and assure progress and timely completion of study goals• Responsible for ensuring clinical trials are conducted in accordance with scientific, medical, and ethical principles, and within regulatory requirements/guidelines• Responsible for volunteer safety and accurate interpretation and execution of research protocols including multiple study activities• Leads the clinical study components with respect to time, operational feasibility, and study-level CRU resources required to deliver individual studies against the development plan (part of the study budget)• Assesses impact of technologies required to deliver clinical trials and incorporates the development of these technologies into the clinical studies to ensure conduct and data collection suitable for purpose• Provides support for Methodology/Mechanistic studies as appropriate• Partners with Core Project Teams to provide study schedule and budget information to enable project management• Identifies performance/quality issues to develop appropriate remediation plan• Identifies and escalates system or process issues affecting deliverables• Manages the creation and detailing of all study activity/source documents• Leads the quality control of all study related activities for assigned protocols• Assures data integrity and data quality in assigned studies• Accountable to CRU leadership for the highest quality of data in clinical trials• Manages all data queries specific to subject data collection• Supports EDCMS setup; assures EDCMS Setup reflects requirements of final approved protocol or approved amendment(s)Assures staff perform necessary data quality and review checks• Reviews data output over the course of the study and escalates any noted issues to the appropriate staff member or line leader• Leads a systematic review of all study data prior to database lock to assure the absence of data issues• May represent the unit on Global initiatives (Global SOP's, process improvement teams, other activities as they present themselves) as they are the subject matter experts in the Unit• May Lead CRU teams in accomplishing business needs and resolving issues• May represent the CRU as a subject matter expert for internal/external resource (provide support to external centre, etc.)• Participate in study and staff scheduling for assigned protocols, as appropriate• May participate in study related data collection activities as needed• Oversee creation and detailing of study activity documents for staff & volunteer use• May mentor/coach other staffQualifications• Minimum of BA/BS in a biomedical discipline or equivalent education/training is required; advanced training/education preferred• Relevant experience in clinical research and drug development with clinical operations experience required• Specific direct experience in early drug development (Phase I and IIa) preferred• Substantial clinical operations and pharmaceutical industry experience in order to have a thorough understanding of the processes associated with executing clinical development plans and addressing related regulatory issues• Experience in Project Management and leadership of matrix teams is essential• Drug development experience including familiarity with: Clinical study management and monitoring, Project/process management, Data management, Clinical & regulatory processes, Regulatory submissions, Budget / expense management, Experience of Vendor Management, Scientific excellence, Administrative excellence, Systems technology• Initiating and Implementing Change: Innovation, Learning Organization, Flexibility and Resilience, Courage with Decisiveness to Act, Problem Solving, Positive approach, forward thinking, challenge the status quo• Matrix leadership skills: Influencing, Collaborative, supportive, Networking and Alliance Building, Personal Leadership, Team work, Communication, Negotiation, Decisive and assertive, Change agile, Able to deal with ambiguity• Proficiency in using MS Office tools suite (Excel, Word,etc.)Additional By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.

11 days ago

Remote Clinical Research Specialist Integrated Resources, Inc

New Haven, Connecticut

Remote

Contractor

Support the randomization process and act as the IWRS PRIMARY AdministratorArranging and participating in the organization of study team meetings Taking minutes and distributingManaging and maintaining study documents and trial supplies, colonoscopy forceps, FedEx envelop, IWRS User information. Contractor will need to train onsite and then be able to work remoteJob description:Provide product training and support to clinical sites for the pill cam procedure.

11 days ago

Clinical Research Support Laboratory Supervisor Actalent Inc

New Haven, CT

$65,000–$101,000 / year

This position operates within a Clinical Research Support Laboratory that serves as a primary, non-CLIA-certified facility for collecting, processing, stabilizing, documenting, shipping, and tracking research biospecimens from patients participating in clinical trials across a cancer center network. This role oversees laboratory technicians and support staff, manages laboratory resources for the collection and processing of clinical research specimens, and ensures strict adherence to protocol, institutional, and safety requirements.

3 days ago

Clinical Research Specialist Integrated Resources, Inc

New Haven, Connecticut

Full time

Support the randomization process and act as the IWRS PRIMARY Administrator• Arranging and participating in the organization of study team meetings Taking minutes and distributing• Managing and maintaining study documents and trial supplies, colonoscopy forceps, FedEx envelop, IWRS User information.• Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields.

11 days ago

Clinical Research Data Coordinator Actalent Inc

New Haven, CT

$32–$35 / hour

3-5+ years of experience in clinical research data management, clinical research data entry, or in a similar role such as Clinical Research Coordinator (CRC), Clinical Research Assistant (CRA), or Clinical Data Coordinator. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

5 days ago

Assistant Director For Clinical Trials Stony Brook University

Stony Brook, NY

Duties: Staff/Personnel Responsibilities: Supervises CRC staff, providing specific work assignments to staff in order to facilitate research at SBU, performing QA on assigned work, carrying out performance programs reviews and evaluations, managing time off requests, etc. Required Qualifications (as evidenced by an attached resume): Bachelor's degree (foreign equivalent or higher) plus three (3) years of full-time experience in clinical research with two (2) years of this working with sponsored clinical trials.

12 days ago

Clinical Research Coordinator U.S. Renal Care, Inc.

Orange, Connecticut

$65,000–$80,000 / year
Full time

1 day ago

YCCI Clinical Research Nurse 2 Yale University

New Haven, CT

$68,000–$120,500 / year

Support the Center's mission of providing the highest quality service to the clinical investigators and study participants, work collaboratively with research support staff, clinical investigators and administration to ensure the professional and accurate performance of participant education, protocol-directed activities, and data collection, while working directly in a nursing capacity including the performance of essential clinical skills, which must be current within one year, with the study participants. Healthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air.

30+ days ago

Ycci Clinical Research Nurse 2 Yale University

New Haven, CT

$68,000–$120,500 / year

30+ days ago

Clinical Research Nurse 1 Yale University

New Haven, CT

$65,000–$101,000 / year

3. Contributes to protocol development, submission, and renewal by collecting written materials and writing procedural documents; ensures ongoing compliance with institutional review board (IRB) policies by monitoring changes in IRB policies related to human specimens and informing the research team of such changes. Contributes to protocol development, submission, and renewal by collecting written materials and writing procedural documents; ensures ongoing compliance with institutional review board (IRB) policies by monitoring changes in IRB policies related to human specimens and informing the research team of such changes.

30+ days ago

Clinical Research Nurse 2 Actalent Inc

New Haven, CT

$50–$55 / hour

The Clinical Research Nurse II provides specialized research nursing services for patients enrolled in oncology and hematology clinical trials, ensuring the safe, compliant, and efficient conduct of moderately to highly complex protocols. Advocate for patients and families by maintaining the integrity of the clinical research study and serving as a clinical resource for triaging and addressing research-related inquiries from institutional websites and professional presentations.

1 day ago

Pathology Clinical Intake Manager and Digital Pathology Operations Lead Yale University

New Haven, CT

$92,000–$146,750 / year

This position oversees and manages all aspects of high-level clinical and administrative support for Anatomic and Clinical Pathologists and their teams, ensuring seamless relationships with the following areas at YSM: Case Management, Laboratories Academic Offices and Research offices. Operationally, this role is responsible for Managing the team that completes the following critical work for the department: Coordinating the administrative aspects of specimen handling, requests for additional materials, and case management resolution, as well as obtaining and organizing required information from referring hospitals and providers.

19 days ago

Pathology Clinical Intake Manager And Digital Pathology Operations Lead Yale University

New Haven, CT

$92,000–$146,750 / year

19 days ago

Clinical research Coordinator New York Cancer and Blood Specialists

Shirley, New York

o Track SAEs & Deviations: Document Serious Adverse Events(SAEs) and deviations, reporting them to the sponsor within 24 hours when• applicable.• o Provide Regulatory Team with Summaries: Share event summaries with the• Regulatory team for timely reporting to regulatory authorities.• o Attend Key Meetings: Participate in Site Initiation Visits (SIVs), research• meetings, and sponsor-specified sessions. o Enroll participants into a Clinical Interventional or Observational Study• o Obtain Informed Consent: Explain study procedures, risks, and benefits to• participants, ensuring full understanding.• o Coordinate Appointments: Organize and schedule research participant• appointments efficiently.• o Manage Research Care: Coordinate care during all research-related appointments,• collaborating with other NYCBS departments.

30+ days ago

Clinical Research Coordinator New York Cancer and Blood Specialists

Shirley, New York

Clinical Research CoordinatorLocation: Shirley, NYHours/Days: 5/8.5 hour shifts, Mon-Fri between 7:30am-6:30p,Organization: New York Cancer & Blood Specialists (NYCBS) . Collect Data: Gather complete and accurate participant data, including medical history, medication review, physical exams, lab tests, ECG, AE review and other required study assessments.

7 days ago

Clinical Research Coordinator (On-Site Only) New York Cancer and Blood Specialists

Shirley, New York

Remote

o Collect Data: Gather complete and accurate participant data, including medical history, medication review, physical exams, lab tests, ECG, AE review and other required study assessments. By offering cutting-edge treatments, innovative research, and a patient-centered approach, we are redefining what’s possible in the fight against cancer and blood disorders.

30+ days ago

Manager, Clinical III - Cardiac Progressive-Intensive Care Unit Saint Francis Health System

New Haven, CT

This statute allows employers to lawfully refuse to hire applicants for safety-sensitive jobs or to discipline or discharge employees who work in safety-sensitive jobs if they test positive for marijuana, even if they have a valid license to use medical marijuana. Minimum Education: Has completed the basic professional curricula of a school of nursing as approved and verified by a state board of nursing, and holds or is entitled to hold a diploma or degree therefrom.

26 days ago

VP IT - Clinical Applications and Engineering Yale New Haven Health

Stratford, Connecticut

Work closely with the DTS leadership team and especially to the executive leadership for patient experience technology platforms (digital front door, access, engagement, and patient-facing applications), ensuring a seamless end-to-end patient experience across the healthcare continuum that is smoothly integrated with the care team experience. Reporting jointly to the 2 Senior Vice Presidents, Chief Information Officer and Chief Digital Health Officer, the VP of Care Team experience in Digital and Technology Solutions (DTS) is responsible for partnering with leaders across Yale New Haven Health System (YNHHS) and Yale University to develop and execute strategies and tactics that leverage information technology to achieve organizational goals.

30+ days ago

VP IT - Patient Experience, Clinical Applications and Engineering Yale New Haven Health

Stratford, CT

30+ days ago

Senior Contracts & Clinical Trials Officer Stony Brook University

Stony Brook, NY

2602026'',''2602026'',''Sponsored Programs Associate II'',''Sponsored Programs Associate II'',''Administrative & Professional (non-Clinical)'',''Administrative & Professional (non-Clinical)'',''US-NY-Stony Brook'',''US-NY-Stony Brook'',''Office of Sponsored Programs'',''Office of Sponsored Programs'',''Full-time'',''Full-time'',''Day Shift'',''Day Shift'',''8.30 a.m. Brief Description of Duties: This role involves drafting, negotiating, and managing research contracts, including clinical trial agreements, testing and laboratory study agreements, research collaborations, and industry-sponsored contracts.

25 days ago

Clinical Technologist 1, Dermatology, Dermatopathology Yale University

New Haven, CT

Under the supervision of the Laboratory Manager and with a thorough knowledge and understanding of clinical laboratory support functions, techniques, processes to ensure excellent patient care services and research support initiatives. Required Education and Experience Four years of related work experience, two of them in the same job family at the next lower level, and a high school level education; or two years of related work experience and an Associate''s degree; or an equivalent combination of experience and education.

30+ days ago

Assistant Director for Clinical Trials Stony Brook University

Stony Brook, NY

12 days ago

Sr. Clinical Trials Transparency & Disclosure Specialist Celldex Therapeutics Inc

New Haven, CT

$87,831–$114,066 / year

Working collaboratively with Clinical Operations, Regulatory Affairs, Biostatistics, Medical Writing, Legal, and other cross-functional stakeholders, the Clinical Trials Transparency & Disclosure Specialist serves as a subject matter expert for transparency and disclosure requirements across the development portfolio. We are committed to compensating employees equitably based on several factors including experience, education, licensure/certifications, skill level, location of the position, and availability of similar talent in a competitive market.

30+ days ago

Research And Clinical Services Librarian Yale University

New Haven, CT

$68,000–$145,250 / year

Reporting to the Associate Director for Research and Scholarly Services, the Research and Clinical Services Librarian leads the law library's dynamic and proactive research, instructional, and reference support to faculty, students, and staff in Yale Law School's expansive clinical program. As a member of the Research and Instructional Services team, the Research and Clinical Services Librarian participates in the faculty liaison program, staffs the reference desk, conducts research consultations, and contributes to the library's instructional program.

30+ days ago

Research and Clinical Services Librarian Yale University

New Haven, CT

$68,000–$145,250 / year

30+ days ago

Supervisor, Clinical (Prem Wknd) - Cardiac Surgical Stepdown Saint Francis Health System

New Haven, CT

30+ days ago

Clinical Practice Specialist 3, Specialty Liaison Yale University

New Haven, CT

$68,000–$120,500 / year

The successful candidate for this position will become a subject matter expert in all areas relating to revenue cycle management with a specific focus on providing ongoing analysis of the health of the revenue cycle for Yale Medicine and assigned clinical specialties with the goal of improving billings and colletions and resolving coding, billing and payer/contracting issues that may be impacting the revenue cycle. Ability to analyze and interpret detailed reports, develop clear conclusions and summarize findings; ability to perform quality assurance on individual accounts, monitor and analyze clinical department and payor key performance indicators and metrics for revenue cycle.

7 days ago

Research & Clinical Writer/Editor, YSM/YM Yale University

New Haven, CT

$65,000–$101,000 / year

The use of AI as a regular part of the editorial workflow to support content development and scalability is critical in this role: it will be used for identifying and organizing source materials; generating and refining structured drafts from transcripts, research publications, and validated sources; critically reviewing content for accuracy and tone; and coordinating expert review prior to publication. The Writer/Editor pitches, researches, and writes news stories, faculty profiles, feature articles, newsletters, and static web content, and conducts interviews with faculty, institutional leaders, and subject matter experts.

30+ days ago

Research & Clinical Writer/Editor, Ysm/Ym Yale University

New Haven, CT

$65,000–$101,000 / year

30+ days ago

Home Health Clinical Manager Humana Inc

Riverhead, NY

$92,600–$127,400 / year

Our care teams include nurses, physical therapists, occupational therapists, speech-language pathologists, home health aides, and medical social workers - all working together to help patients rehabilitate, recover and regain their independence so they can live healthier and happier lives. As the largest provider of senior-focused primary care, a leading provider of home healthcare and a leading integrated home delivery, specialty, hospice and retail pharmacy, CenterWell is focused on whole health and addressing the physical, emotional and social wellness of our patients.

18 days ago

Clinical Lab Technologists IV Cytotechnologist - Per Diem Stony Brook University

Stony Brook, NY

2601889'',''2601889'',''TH Clinical Laboratory Technologist IV'',''TH Clinical Laboratory Technologist IV'',''Laboratory'',''Laboratory'',''US-NY-Stony Brook'',''US-NY-Stony Brook'',''Cytology'',''Cytology'',''Per Diem'',''Per Diem'',''Variable'',''Variable'',''variable'',''variable'',''Sat, Sun, Variable'',''Sat, Sun, Variable'',''May 26, 2026'',''May 26, 2026'',''Aug 25, 2026, 4:59:00 AM'',''Aug 25, 2026, 4:59:00 AM'',''$68.98'',''$68.98'','''','''',''SL1'',''SL1'',''Stony At Stony Brook Medicine, a Clinical Laboratory Technologist / Cytotechnologist is a valuable member of our team, who provides clinical services to our patient population, and will also interact in a professional manner with physicians, nursing staff, support staff, peers and other members of the hospital community.

30+ days ago

Clinical Laboratory Technologist/Technician -Histology Stony Brook University

Stony Brook, NY

$96,406–$122,265 / year

At Stony Brook Medicine, a TH Clinical Laboratory Technologist/Technician is a valuable member of our team, who provides clinical services to our patient population and follows all laboratory procedures and protocols with interpretation of such policies as necessary to ensure proper patient care and safe work equipment. This means that when the Hospital is faced with an institutional emergency, employees in such positions may be required to remain at their work location or to report to work to protect, recover, and continue operations at Stony Brook Medicine, Stony Brook University Hospital and related facilities.

6 days ago

Clinical Nutrition Manager - Registered Dietitian St. Catherine of Siena Medical Center

Smithtown, NY

$89,000–$105,000 / year

Provide leadership and oversight of daily clinical nutrition services for assigned inpatient and ambulatory care areas, ensuring high-quality, patient-centered care. The Clinical Nutrition Manager provides leadership and oversight for the delivery of high-quality clinical nutrition services across assigned inpatient and ambulatory care areas.

27 days ago

Clinical Nutrition Manager - Registered Dietitian Catholic Health

Smithtown, New York

$89,000–$105,000 / year

Job Details: The Clinical Nutrition Manager provides leadership and oversight for the delivery of high-quality clinical nutrition services across assigned inpatient and ambulatory care areas. Provide leadership and oversight of daily clinical nutrition services for assigned inpatient and ambulatory care areas, ensuring high-quality, patient-centered care.

28 days ago

Associate Clinical Oncology Specialist Natera Inc

Bridgeport, CT

$110,000–$130,000 / year

The compensation package listed is for 1st year OTE, which are based on a wide array of factors unique to each candidate, including but not limited to skill set, years & depth of experience, certifications and specific office location. Responsibilities include cultivating and maintaining key relationships and working with customers and internal partners that enable Signatera patient retention and unit growth within existing customers.

5 days ago

Clinical Research Coordinator 2 Yale University

New Haven, CT

$65,000–$101,000 / year

Healthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air. HCW have specific health requirements that must be met prior to starting work, including MMR vaccine or immunity, varicella (chickenpox) vaccine or immunity, TB screening, COVID vaccine according to University policy, hepatitis B vaccine or immunity, and annual flu vaccination.

30+ days ago

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Clinical Jobs in Riverhead, NY

Clinical Research Coordinator U.S. Renal Care

Gynecologist, Clinical Assistant/Associate Professor, OBGYN, Minimally Invasive Gynecologic Surgery Stony Brook University SUNY

Global Women's Health Fellowship, Clinical Instructor, OBGYN Stony Brook University SUNY

RN - Nursing Yale New Haven Health

Senior Finance Manager, Clinical Research Yale University

YCCI Clinical Research Technical Trainer Yale University

Clinical Research Support Laboratory Manager Actalent Inc

Clinical Research Associate I Stony Brook University

Clinical Research Assistant Stony Brook University

Director of Administration, Cancer Clinical Trials Office Stony Brook University

Director Of Administration, Cancer Clinical Trials Office Stony Brook University

Clinical Research Nurse 2 Yale University

Cancer Clinical Trials Finance Manager Stony Brook University

Senior Clinical Data Manager Celldex Therapeutics Inc

Clinical Program Manager Integrated Resources, Inc

Remote Clinical Research Specialist Integrated Resources, Inc

Clinical Research Support Laboratory Supervisor Actalent Inc

Clinical Research Specialist Integrated Resources, Inc

Clinical Research Data Coordinator Actalent Inc

Assistant Director For Clinical Trials Stony Brook University

Clinical Research Coordinator U.S. Renal Care, Inc.

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