444 Results for

Clinical Jobs in East Northport, NY

Jobs

RN Pediatric Clinical Research - PRN Professional Case Management

White Plains, NY

Please contact Ashley Sin at (303) 317-5486 x486 or at ashley.sin@emvenio.com today to learn more about our opportunities where you can make a difference in your own career! Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw, IVs, and Subcutaneous Injections (date of last practice within 6 months, preferred).

Today

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.

27 days 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.

Today

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.

12 days ago

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

Stony Brook, NY

Job Description Job Description Job Opportunity: Assistant/Associate Professor in Minimally Invasive Gynecology Our organization is seeking a dedicated full-time faculty member at the Assistant or Associate Professor level to enhance our thriving academic practice in Minimally Invasive Gynecology (MIGS). It includes a comprehensive hospital system, specialized children's hospital, and multiple health sciences schools, along with numerous community healthcare settings throughout the region.

Today

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.

17 days ago

Clinical Manager, Nurse Practitioner VNS Health

Bronx, NY

Minimum of three years of clinical experience in treating clients in a behavioral health setting requiredFor Certified Community Behavioral Health Clinic (CCBHC): Minimum of one years’ experience in a substance use treatment setting, evaluating patients with substance use disorders & prescribing medications for addiction treatment. Powered and informed by data analytics that are unmatched in the home and community-health industry, VNS Health offers a full range of health care services, solutions and health plans designed to simplify the health care experience and meet the diverse and complex needs of the communities and people we serve in New York and beyond.

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

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.

Today

Home Health Clinical Manager CenterWell Home Health

Hauppauge, 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.

Today

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

Program Manager Clinical Research Montefiore Medical Center

$84,000–$105,000 / year

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

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.

27 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

RN Pediatric Clinical Research - PRN Act for Health

White Plains, New York

5 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

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

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

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

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.

3 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.

3 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.

17 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

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.

3 days ago

Manager, Clinical Imaging Operations Regeneron Pharmaceuticals

Tarrytown, NY

$128,600–$210,000 / year

Study maintenance: Track imaging progress during clinical studies and address imaging issues that may come up in close collaboration with clinical study teams, sites, and imaging CROs, including functional oversight through day to day monitoring of key performance indicators related to imaging timeliness, quality, etc., query resolution and troubleshooting. You should expect to work closely with our imaging vendor partners, the clinical operations function, the data management function, external clinical research organizations (CROs), and clinical sites to ensure the successful completion of startup activities, ongoing execution, and close-out of clinical studies.

30+ 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

Clinical Research Coordinator New York Medical College

Hawthorne, New York

Full time

Overview: The Division of Medical Genetics at New York Medical College is seeking a clinical research coordinator to work with our team on multiple clinical trials. Must be adept at keeping track of multiple projects, able to work independently, and have strong problem solving, communication, and analytical skills.

15 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

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.

11 days ago

Payer Stars/Quality Clinical Consultant, Senior Manager PwC

Melville, NY

$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 .

9 days ago

Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLP

Melville, NY

$124,000–$280,000 / year

30+ days ago

Clinical Research Coordinator I Montefiore Medical Center

$53,040–$66,300 / year

This includes developing workflow for patient care such as assigning secretaries to schedule patients, developing workflow with ancillary departments (such as radiology, advanced imaging, pathology, pharmacy), and assigning appropriate clinical team members such as doctors to complete clinical tasks such as reviewing adverse events versus assigning non-clinical team members to complete non clinical tasks such as administering questionnaires to a patient. Clinical Research Coordinator I will oversee multiple clinical trials, investigator-initiated studies, and quality improvement projects within the department of Neurology, serving as a point person for patients, their family members and the clinical study team.

30+ days ago

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

Norwalk, CT

$29.65–$55.55 / hour

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.

6 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 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

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

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.

4 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.

26 days ago

Clinical research Coordinator New York Cancer and Blood Specialists

Shirley, New York

30+ 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

Executive Medical Director, Clinical Program Lead, Immunology / Rheumatology Regeneron Pharmaceuticals Inc

$390,000–$527,600 / year

Discover your role: Acts as medical expert and leader in interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards. Uses excellent scientific standing among peers and the ability to address issues with scientific rigor and creative solutions; uses that creativity and knowledge to build and defend data-driven plans and decisions, both with internal scientific management and the Company's partners/collaborators.

4 days ago

Executive Medical Director, Clinical Program Lead, Hematology Oncology Cell Therapy Regeneron Pharmaceuticals

Tarrytown, NY

$390,000–$527,600 / year

30+ days ago

Executive Medical Director, Clinical Development, Hematology Cell Therapy Regeneron Pharmaceuticals Inc

$390,000–$527,600 / year

A typical day in the life may include the following: Acts as medical expert and leader in interactions with external collaborators (e.g., regulatory authorities, key opinion leaders, advisory boards, patient advocacy groups), internal collaborators (e.g., Research, Early Clinical Development, Global Medical Affairs, Marketing, HEOR), and internal decision boards. This role requires an impactful and highly hard-working individual who serves as a clinical role model for the team and demonstrates outstanding clinical scientific knowledge applicable to hematology clinical research.

30+ days ago

Medical Director, Clinical Development, Solid Tumor Oncology Regeneron Pharmaceuticals

Tarrytown, NY

$284,900–$385,700 / year

The Medical Director, Clinical Sciences, Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial protocols and is responsible for medical/scientific supervision of individual clinical trials.

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

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

Resume Resources

Free Resume Templates Free Resume Builder

Get noticed by top employers!

Upload your resume to let employers know you're open to Clinical job opportunities. Plus, receive relevant job recommendations in your inbox.

Create A Free Account

Clinical Jobs in East Northport, NY

RN Pediatric Clinical Research - PRN Professional Case Management

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

Dialysis Clinical Manager Registered Nurse - RN Fresenius Medical Care

Associate Director, Clinical Development Trial Lead (CDTL) Joulé

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

RN Clinical Reviewer Greenlife Healthcare Staffing

Clinical Manager, Nurse Practitioner VNS Health

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

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

Home Health Clinical Manager CenterWell Home Health

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

Program Manager Clinical Research Montefiore Medical Center

Senior Finance Manager, Clinical Research Yale University

YCCI Clinical Research Technical Trainer Yale University

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

Clinical Research Associate I Stony Brook University

RN Pediatric Clinical Research - PRN Act for Health

Clinical Research Assistant Stony Brook University

Clinical Research Nurse 2 Yale University

Director Of Administration, Cancer Clinical Trials Office Stony Brook University

Director of Administration, Cancer Clinical Trials Office Stony Brook University

Clinical Program Manager Integrated Resources, Inc

Remote Clinical Research Specialist Integrated Resources, Inc

Cancer Clinical Trials Finance Manager Stony Brook University

Manager, Clinical Study Lead Regeneron Pharmaceuticals Inc

Manager Clinical Study Lead Regeneron Pharmaceuticals Inc

Clinical Research Specialist Integrated Resources, Inc

Manager, Clinical Imaging Operations Regeneron Pharmaceuticals

Senior Manager Clinical Study Inspection Readiness Regeneron Pharmaceuticals Inc

Clinical Research Coordinator New York Medical College

Senior Clinical Data Manager Celldex Therapeutics Inc

RN Clinical Research Hartford HealthCare Corp

Payer Stars/Quality Clinical Consultant, Senior Manager PwC

Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLP

Clinical Research Coordinator I Montefiore Medical Center

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

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

Clinical Research Nurse 1 Yale University

YCCI Clinical Research Nurse 2 Yale University

Ycci Clinical Research Nurse 2 Yale University

Assistant Director For Clinical Trials Stony Brook University

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

Clinical research Coordinator New York Cancer and Blood Specialists

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

Executive Medical Director, Clinical Program Lead, Immunology / Rheumatology Regeneron Pharmaceuticals Inc

Executive Medical Director, Clinical Program Lead, Hematology Oncology Cell Therapy Regeneron Pharmaceuticals

Executive Medical Director, Clinical Development, Hematology Cell Therapy Regeneron Pharmaceuticals Inc

Medical Director, Clinical Development, Solid Tumor Oncology Regeneron Pharmaceuticals

Program Manager, Ambulatory Clerkships and Clinical Skills Hofstra University

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

Resume Resources

Similar Job Searches

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