353 Results for

Clinical Jobs in Monroe, CT

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.

27 days ago

Clinical Program Director of Residential Services Mitchell Martin

Waterbury, CT

$45–$50 / hour

By applying for this job, you agree to receive AI-generated calls, text messages, and/or emails from Mitchell Martin Inc and its affiliates and contracted partners at various frequency through traditional and automated methods. • The Clinical Program Director oversees residential behavioral health services, ensuring high-quality care for individuals with mental health and substance use disorders.

5 days ago

Clinical Director Mitchell Martin

Stamford, CT

$100,000–$120,000 / year

By applying for this job, you agree to receive AI-generated calls, text messages, and/or emails from Mitchell Martin Inc and its affiliates and contracted partners at various frequency through traditional and automated methods. Clinical Director - Stamford, CT Onsite - Full Time - $100,000-$120,000 Per Year.

13 days 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.

12 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.

6 days 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.

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

Clinical Research Coordinator - Danbury Hospital Clinical Trials department - Danbury, CT Nuvance Health

Danbury, CT

$29.65–$55.55 / hour

Our team of more than 15,000 caregivers delivers compassionate care through seven community hospitals, primary care and specialty practice locations, outpatient settings, home care services and telehealth visits. 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.

30+ days ago

Per Diem Clinical Research Nurse - Home Visits Science 37 Inc

Hartford, CT

$50–$55 / hour

With interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.

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

Per Diem Clinical Research Nurse - Home Visits Science 37

Hartford, CT

$50–$55 / hour

30+ days ago

Clinical Research Associate - Clinical Research Center Hartford HealthCare Corp

Hartford, CT

This includes but is not limited to; research conduct, budget negotiation & management, initiating collaborations with other investigators and areas pertinent to the performance of the study, monitoring research progress and making necessary changes towards process improvement, leading efforts to initiate new studies, attending IRB meetings to expedite the start-up process. Promotes and monitors lower level personnel regarding the ethical conduct of research by assuring that good faith suspicions of misconduct in research as defined within Research Administrations Policy and other misconduct as described in HHC Code of Conduct are reported appropriately.

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

Clinical Program Manager, Clinical Education Jackson Laboratory

Farmington, CT

Remote

$65,018–$108,857 / year

JAX Clinical Education (www.jax.org/ccep) develops and disseminates clinical education for professional and trainee audiences across the country, preparing clinicians to evaluate and apply genomic in practice, as part of JAX's broader Genomic Education work spanning learners from high school through scientists. You will bring a nursing lens and prior experience in nursing education to JAX's Clinical Education programs, working collaboratively with genomics experts, instructional designers, and educators to turn complex science into effective learning that makes a difference.

8 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

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).

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 Coordinator I Ora

Hartford, CT

Perform various tasks (post-onboarding) such as use of proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments. Our CRC I's will partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.

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

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 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 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

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

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.

11 days ago

Clinical Research Coordinator I Ora, Inc.

Hartford, CT

30+ 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 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

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

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

Clinical Nurse Manager (RN) Healogics

Hartford, Connecticut

Organizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licenced Practical Nurses (LPNs) or Licensed Vocational Nurses (LVNs); Certified Medical Assistants (CMAs); etc. May be required to provide case management to a group of patients providing specific assessments according to protocols and procedures, clinical competence in procedural skills, treatments, and patient/caregiver education related to wound care management.

12 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 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

Clinical Research RN Hartford HealthCare Corp

Hartford, CT

Your Responsibilities • Conduct clinical research studies, including data collection and data entry • Collaborate with cross-functional teams, including researchers, clinicians, and administrators • Develop and implement research protocols and procedures • Ensure compliance with regulatory requirements and institutional policies • Participate in research-related meetings and presentations. Job Description Primary Location: Connecticut-Hartford-560 Hudson St HH E&R Ctr (10058) Job: Nursing Organization: Hartford HealthCare Corp.

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 Nurse Manager (RN) Healogics Inc

Hartford, CT

$83,000–$111,900 / year

Organizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licenced Practical Nurses (LPNs) or Licensed Vocational Nurses (LVNs); Certified Medical Assistants (CMAs); Hyperbaric Oxygen Technicians, etc. May be required to provide case management to a group of patients providing specific assessments according to protocols and procedures, clinical competence in procedural skills, treatments, and patient/caregiver education related to wound care management.

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.

11 days ago

Pathology Clinical Intake Manager And Digital Pathology Operations Lead Yale University

New Haven, CT

$92,000–$146,750 / year

11 days ago

Clinical Sales Specialist, Electrophysiology - LAAO (Connecticut) Abbott

Connecticut

Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Driving a personal auto or company car or truck, or a powered piece of material handling equipment . In this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures.

6 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 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

Manager Clinical Invasive Cardiology - Registered Nurse Northwell Health

Danbury, CT

$52.03–$96.62 / hour

Responsible for daily operations of cardiac catheterization laboratories, including, but not limited to: scheduling of staff; triaging resources to assure timely, quality care delivery; resolving equipment, information systems, and facility problems; responding to internal and external customer demands; and, collaborating with other hospital departments to coordinate patient care. Participates in department, division, and Danbury Hospital' operational strategy planning and development as it relates to the cath labs, including working with other sections to develop plans to maximize operational efficiencies by developing, growing, and maintaining high quality cardiovascular services.

30+ days ago

Clinical Operations Manager (Greenwich, CT) Oula

Connecticut

Process Architecture: Build, refine, and scale clinic workflows (e.g., patient check-in, inventory management, team file organization) to meet the needs of a growing practice. Oula is seeking a Clinical Operations Manager to lead the daily execution and long-term growth of our new Greenwich, Connecticut maternity clinic.

5 days ago

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

Norwalk, CT

$29.65–$55.55 / hour

30+ days ago

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Clinical Jobs in Monroe, CT

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

Clinical Program Director of Residential Services Mitchell Martin

Clinical Director Mitchell Martin

Associate Director, Clinical Development Trial Lead (CDTL) Joulé

Clinical Lab Assistant Joulé

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

Senior Finance Manager, Clinical Research Yale University

YCCI Clinical Research Technical Trainer Yale University

Clinical Research Coordinator - Danbury Hospital Clinical Trials department - Danbury, CT Nuvance Health

Per Diem Clinical Research Nurse - Home Visits Science 37 Inc

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

Per Diem Clinical Research Nurse - Home Visits Science 37

Clinical Research Associate - Clinical Research Center Hartford HealthCare Corp

Clinical Research Nurse 2 Yale University

Clinical Program Manager, Clinical Education Jackson Laboratory

Clinical Research Associate I Stony Brook University

RN Pediatric Clinical Research - PRN Act for Health

Clinical Research Assistant Stony Brook University

Clinical Research Coordinator I Ora

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