318 Results for

Clinical Jobs in Stony Brook, NY

Jobs

Physician Assistant/Nurse Practitioner (APP), Clinical Instructor, Neurosurgery, General Neurosurgery Service Stony Brook University

Stony Brook, NY

Full time

It encompasses Stony Brook University Hospital, Stony Brook Children's Hospital, the five Health Sciences schools -- Dental Medicine, Health Technology and Management, 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. Includes routine and emergency consultations in collaboration with the on-call attending, daily management, coordination of care, patient and family counseling, ordering and interpreting diagnostic testing as well as routine and emergent bedside procedures such as lumbar puncture, ventriculoperitoneal shunt tap, placement of ICP monitor, ventriculostomy, and lumbar drain.

28 days ago

Clinical Psychologist (PhD / PsyD) – Outpatient Behavioral Health Jobot

Fairfield, CT

$100,000–$140,000 / year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Stable, full-time W2 role with steady caseload, multidisciplinary support, psychological testing opportunities, and growth into leadership/clinical supervision—plus strong benefits and work-life balance.

1 day ago

Dialysis Clinical Manager Registered Nurse - RN Fresenius Medical Care

Hicksville, NY

$90,709–$151,091 / year

As the facility leader, you will be part of a close-knit, collaborative team responsible for delivering unique care plans and providing dialysis treatment to patients facing end stage renal disease or chronic kidney disease. We have a diverse range of employee resource groups (ERGs) to encourage employees with similar interests, goals, social and cultural backgrounds, or experiences to come together for professional and personal development, discussion, activities, and peer support.

1 day ago

Associate Director, Clinical Development Trial Lead (CDTL) Joulé

Stamford, CT

$104.63 / 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.

13 days ago

Clinical Lab Assistant Joulé

Stamford, CT

$25–$32 / hour

General lab duties to include the following: preparing lab coats, assuring clean laundry for all study needs, use clinical instruments as needed, product application, training to use scientific scale to collect product weights pre- and post-study, hot room pad collection, and washing subject’s legs and arms for multiple study protocols. Assist Clinical Coordinators in preparing and executing clinical studies which support product claims for Beauty Care, Laundry and Adhesive businesses.

7 days ago

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.

1 day ago

RN Clinical Reviewer Greenlife Healthcare Staffing

Jericho, NY

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.

18 days ago

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.

1 day ago

Clinical Chemistry Pathology position at UPMC Presbyterian in Pittsburgh, PA UPMC Southwestern PA

Brentwood, NY

Assistant Professor (1-5 years of experience) Associate Professor (6-10 years of experience) About The Department of Pathology and UPMC All Divisions in Laboratory Medicine have a strong interest in service, research and education UPMC is a $23 billion world-renowned health care provider and insurer 92,000 employees, including 4,900 physicians Over 40 academic, community and specialty hospitals Over 800 doctors' offices and outpatient sites UPMC is inventing new models of accountable, cost-effective, patient-centered care Closely affiliated with University of Pittsburgh About the Community Pittsburgh is a vibrant, mid-sized city with the feel of a small town. Key Highlights Join a department total of 131 Pathologists with 4 in the clinical chemistry lab Provides technical directorship of the clinical laboratories to ensure regulatory compliance and quality patient test results within an integrated multi-hospital clinical chemistry service.

1 day ago

Home Health Clinical Manager CenterWell Home Health

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.

1 day ago

Registered Nurse Care Manager / Case Management (RN) Yale New Haven Health

Stamford, CT

Prefer clinical working experience as a NP/PA within the given specialty/service line recommended, but not required APRNs, PAs, CRNAs and CNMs are required to be appointed to the Affiliated Medical Staff of a YNHHS Hospital and credentialed through the Medical Staff process . LICENSURE Active PA Certification by the National Commission of Certification of Physician Assistants (NCCPA), Connecticut State Physician Assistant License OR Connecticut State Registered Nurse License, Connecticut State Nurse Practitioner License .

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.

28 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

Senior Manager Clinical Study Lead (Clinical Experimental Sciences) Regeneron Pharmaceuticals

Armonk, NY

$150,500–$245,500 / year

The CES Ops portfolio is dynamic in nature; study types include, but are not limited to, less complex data transfer agreements, retrospective sample/data acquisition studies to more complex prospective studies including sample/data acquisition, biomarker/technology/method validation, genotypic/phenotypic call back studies, and challenge/screening studies. A typical day in this role looks like: Leads the cross-functional study team responsible for clinical study/research collaboration delivery and is the primary point of contact of leadership and oversight (as required) for the assigned study.

30+ 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.

18 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.

4 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.

4 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.

4 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

Manager, Clinical Study Lead Regeneron Pharmaceuticals Inc

Armonk, NY

$128,600–$210,000 / year

Assigns tasks to Clinical Study Management staff and supports their deliverables; directly supervises CTM staff (work assignments, performance management, recruitment, professional development, coaching, mentoring, ongoing training and compliance, and study support/oversight); recommends and participates in cross-functional and departmental process improvements; and identifies innovative, globally informed approaches to study execution and continuous improvement of CTM SOPs. Discover your role: Leads the cross-functional study team responsible for clinical study delivery, serving as the primary point of contact for leadership and oversight, and oversees execution against planned timelines, deliverables, and budget while raising issues (conduct, quality, timelines, budget) to the Program Operations Lead and stakeholders and implementing corrective actions.

30+ days ago

Manager Clinical Study Lead Regeneron Pharmaceuticals Inc

Armonk, NY

$128,600–$210,000 / year

4 days ago

Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLP

Stamford, CT

$124,000–$280,000 / year

As a Payer STARS/Quality Clinical Consultant, Senior Manager, you will engage with clients in the health services sector, providing strategic guidance and operational consulting to enhance their clinical quality and performance metrics. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .

30+ days ago

Payer Stars/Quality Clinical Consultant, Senior Manager PwC

Melville, NY

$124,000–$280,000 / year

10 days ago

Senior Manager Clinical Study Inspection Readiness Regeneron Pharmaceuticals Inc

Armonk, NY

$150,500–$245,500 / year

This role is expected to leverage Artificial Intelligence (AI)-powered tools - including large language model (LLM) applications such as Claude - to accelerate deliverable production, strengthen documentation quality, and drive continuous improvement in inspection readiness operations, with all AI-assisted outputs subject to human review and full GCP compliance. A typical day in this role looks like: Serve as: CTM Inspection Readiness point of contact leading GCP inspection readiness programs across complex, multi-program clinical portfolios involving both internal teams including CRO partners, and Inspection Management.

30+ days ago

RN Clinical Research Hartford HealthCare Corp

Fairfield, CT

In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial. Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.

12 days ago

Clinical Research Coordinator - Norwalk Hospital Cancer Research - Norwalk, CT Northwell Health

Norwalk, Connecticut

Strong attention to detail and organizational skills • Outstanding interpersonal skills License, Registration, or Certification Requirements: • Basic Life Support current or willing to take course • Valid Driver’s license • Prefer: Professional research certification • Prefer: Basic Life Support Salary Range: $29.65 - $55.55 hourly (Pay based on years of relative experience). Performs procedures including EKG, Phlebotomy, blood and body fluid sampling, packing and shipment of human samples, body measurements and examinations within scope of practice and training, consistent with clinic and study specific policies/procedures and scope of care under the guidance of the supervisor.

19 days 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

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

Ycci Clinical Research Nurse 2 Yale University

New Haven, CT

$68,000–$120,500 / year

30+ 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.

5 days ago

Associate Director, Clinical Development Trial Lead (CDTL) Integrated Resources, Inc

Stamford, CT

The Associate Director, Clinical Development Trial Lead (CDTL) independently leads the cross-functional study team in the development and execution of complex clinical trials and is accountable both regionally and globally to deliver clinical milestones on trial(s) with quality, on time, and within Product and budget. Independently drive and influence local, regional and global, cross-functional study team throughout study implementation, execution and closure empowering them to meet the clinical trial deliverables, including proactive issue management, contingency planning and issue resolution.

30+ 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 (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.

27 days ago

Clinical Trial Transparency & Disclosure Manager (On-site/Hybrid) Boehringer Ingelheim

Ridgefield, CT

$115,000–$181,000 / year

This role requires a strong, solid understanding of and experience with the subject matter, including ability to create and deliver related training to both internal and external business partners as well as it must be able to establish and maintain collaborative working relationships with internal stakeholders (including and especially Clinical study teams) as well as external third-party vendors. This role is responsible for driving the quality, compliance, completeness and timeliness of CDO’s reporting outputs to the US Compliance and Integrity function, through alignment with US CDO leadership and cross-functional stakeholders, to ensure CDO meets the PPSA US regulatory obligation.

30+ days ago

Program Manager, Ambulatory Clerkships and Clinical Skills Hofstra University

Hempstead, NY

$66,300–$70,000 / year

Responsibilities Responsibilities include but are not limited to: Collaborates with the Integrated Learning team, Clinical Experiences team, Testing Manager, Clinical Skills faculty, Center for Learning and Innovation staff, Director of Ambulatory Clerkships, Associate Deans for Medical Education, and Data and Analytics staff to plan, implement, and evaluate ambulatory clerkships and clinical skills programs in accordance with the mission and goals of the organization. The Ambulatory Clerkships include longitudinal ambulatory clinical experiences spanning the first and second years of medical school in the specialties of medicine, obstetrics and gynecology, surgery, pediatrics, and psychiatry, as well as elective experiences in medicine and pediatrics during the third year.

30+ days 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.

12 days ago

Pathology Clinical Intake Manager And Digital Pathology Operations Lead Yale University

New Haven, CT

$92,000–$146,750 / year

12 days ago

Clinical Trials Manager Yale University

New Haven, CT

$82,000–$131,500 / year

Works closely with leadership, internal and external colleagues and community residents to develop new initiatives to support the strategic direction of the organization and implements long-term goals and objectives to achieve the successful outcome of the program. Identifies and evaluates potential future funding sources, and contributes to the submission of grants and contracts supporting the program, including the annual submission and writing of all content areas and budgetary sections of grant applications.

30+ days ago

Clinical Analyst, Population Health & CARE Solutions IQVIA

Greenwich, Connecticut

Cedar Gate Technologies, an IQVIA business, is seeking a clinically experienced healthcare professional who brings both deep care delivery expertise and the ability to work alongside product and engineering teams to improve technology-enabled workflows. As the Clinical Analyst, Population Health & CARE Solutions , you will partner directly with healthcare clients to operationalize CARE solutions, translating real-world clinical and value-based care requirements into practical system configuration and workflow design.

12 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.

19 days ago

Assistant Nurse Manager - Medicine/Telemetry, Full-Time, Nights Clinical or Leadership Cert Required NYU Langone Medical Center

Mineola, NY

$151,049.99–$151,050 / year

Ability to apply nursing process toward achievement of specific outcomes in an organized fashion to address patient/family satisfaction and quality indicators, Evidence of excellent communication (both oral and written), interpersonal, organization, critical thinking, problem solving, and leadership skills, Basic Life Support Certification through the American Heart Association, Physical stamina, manual, dexterity, visual and aural acuity to perform responsibilities. To qualify you must have a Current Registered Professional Nurse licensure in New York State, Baccalaureate degree in Nursing, 2 Years experience required, Clinical certification in the patient population served or nurse leader certification .

30+ days ago

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

Stratford, CT

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

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

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.

18 days ago

Manager Cardio Clinical Operations Northwell Health

Norwalk, CT

$52.03–$96.62 / hour

Assigns work and sees that it is carried out correctly and efficiently; identifies and implements technology to improve operations; maintains accurate and current files on all department budgets, capital equipment request and programs related to operational issues; acts as a liaison between attending physicians, patients, visitor's guests and staff; demonstrates ability to answer any questions that might arise when dealing with patients, physicians, or any matters regarding the department/division/physician office. Oversees scheduling (vacation, holidays) and ensures adequate coverage at all times; performs related personnel functions; ensures staff members understand their roles and responsibilities; supports continued growth of staff and offers opportunities for advancement; assists in developing and maintaining objectives, policies and procedures to ensure the efficient operation of the department/division; strives to streamline operations and effectively apply new concepts and techniques for positive outcomes; identifies and implements technology to improve operations.

30+ days ago

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