410 Results for

Clinical Jobs in Ridgefield, 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 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

Dialysis Clinical Coordinator, Home Therapy U.S. Renal Care

Poughkeepsie, NY

$85,100–$127,651

Knowledge of and remain current with federal, state, local laws and regulations, including health care professionals practice act requirements, in relation to home dialysis program and patient care requirements. Work with Administrator to maintain chronological, thorough, and appropriate documentation in the patient record of all treatments, activities, and communication with the patient, physician and other healthcare professionals.

20 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

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

Clinical Research Coordinator - Clinical Research Department - Poughkeepsie, NY Northwell Health

Poughkeepsie, NY

$29.65–$55.55 / hour

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. Northwell is the largest not-for-profit health system in the Northeast, serving residents of New York and Connecticut with 28 hospitals, more than 1,000 outpatient facilities, 22,000 nurses and over 20,000 physicians.

30+ days ago

Senior Clinical Study Manager Integrated Resources, Inc

Woodcliff Lake, New Jersey

Full time

Job DescriptionProvide operational leadership for assigned trials executing them on time and within budgetOverall coordination and management of clinical trials from startup to closeoutLiaise with other functional areas to identify issues, evaluate and make sound business decisions and ensure implementation of timely solutions. Communicate with Principle Investigator, Study Co-Coordinator, and/ CRO (if applicable) to proactively recognize problem situations and work with other team members as required to resolve issuesManage the publication process in conjunction with the publications team to assure that submission timelines are met.

3 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

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

Senior Clinical Data Manager Integrated Resources, Inc

Woodcliff Lake, New Jersey

Full time

Qualifications• Bachelor degree or above in scientific or related field Minimum 5-7 years' experience in Data Management with experience in managing projects, project teams• Experience with In-Form or other EDC software is desirable however, should have some experience in supporting Oncology studies• Must be able to work independently• Proficiency on all related regulations, GCP, and Good Clinical DM Practice• Project management skills required• Strong oral and written communication skills. Senior Clinical Data ManagerIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.

3 days ago

Clinical Data Manager Integrated Resources, Inc

Woodcliff Lake, New Jersey

Contractor

Perform DM activities for in-house and outsourced trials: protocol review, CRF development, database set up activities, data validation process (including manual data review of listings), SAE reconciliation, managing local laboratory and external labs and database lock. Bachelor degree or above in scientific or related field Minimum 5-7 years' experience in Data Management with experience in managing projects, project teams.

3 days ago

Clinical Research Coordinator - Clinical Research department in Poughkeepsie, NY Nuvance Health

Poughkeepsie, NY

$29.65–$55.55 / hour

30+ days ago

Clinical Research Scientist Integrated Resources, Inc

Woodcliff Lake, New Jersey

Contractor

IT Life Sciences Allied Healthcare CROCertified MBE | GSA - Schedule 66 I GSA - Schedule 621I(DIRECT BOARD) # 732-844-8716 (F) 732-549-5549 Clinical Research ScientistIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.

3 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 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 Nurse Actalent Inc

Paramus, NJ

$54–$60 / hour

This role serves as a key liaison among principal investigators, sub-investigators, clinical research nurses, regulatory specialists, and study patients, supporting trial feasibility, regulatory submissions, patient recruitment and education, and accurate documentation of all study-related activities. Assist principal investigators in preparing proposed clinical trials by reviewing trial protocols, contacting departments that will provide study resources, and ensuring appropriate departments are notified and receive trial documentation, including scientific merit and accrual potential.

5 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 Hackensack Meridian Health

Hackensack, New Jersey

Schedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records are adequate and available for the visit; Meets with monitor at least once during each monitor site visit and resolves all issues found during visit. Responsibilities: A day in the life of a Clinical Research Coordinator at Hackensack Meridian Health includes: Acts as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within the protocol.

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

Clinical Research Coordinator-Full-time-Onsite Holy Name Medical Center

Teaneck, NJ

$50,003.20–$67,496 / year
Full time

The Coordinator oversees study activities from start-up through close-out, including regulatory submissions, participant screening and enrollment, study visit coordination, data and document management, and ongoing communication with investigators, sponsors, IRBs, and internal clinical teams. Holy Name is New Jersey's only independent Catholic health system, comprising a 361-bed acute care hospital, a renowned cancer center, a state-of-the-art fitness center, a residential hospice, a prestigious nursing school, and an extensive physician network.

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 Hackensack Meridian Health

Hackensack, New Jersey

Full time

Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential. Performs nursing assessments and monitors study patient`s progress during clinical trials; Tracks study patient`s response by documenting on toxicity flow sheet, medication flow sheet and nurses` progress notes.

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

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

New City, NY

$71,900–$189,000 / year

Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.

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

Senior Trauma Clinical Data Coordinator - Full Time - Day Hackensack University Medical Center

Hackensack, NJ

A day in the life of a Senior Trauma Clinical Data Coordinator at Hackensack Meridian Health includes: Works in collaboration with Trauma principal investigators, sub-investigators, Trauma Research RN, and regulatory specialists on all research issues ensuring adherence to trauma research protocols. Education, Knowledge, Skills and Abilities Required: Bachelor of Arts/Bachelor of Science diploma/degree in science or healthcare field OR minimum of 4+ years of experience in a related area with High School diploma, general equivalency diploma (GED), and/or GED equivalent programs.

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

Clinical Research Coordinator Lead Nuvance Health

Poughkeepsie, NY

$33.21–$61.68 / hour

Evaluates trial protocols, manages the clinical research sites including, but not limited to acting as primary contact for clinical research sites for questions related to the protocol conduct protocol, regulatory document completion, study supplies, client scheduling, and electronic data capture. 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.

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 Data Coordinator Hackensack Meridian Health

Hackensack, New Jersey

Full time

Works daily in collaboration with other research team members including but not limited to Principal Investigators, Research Nurse Coordinators, Clinical Research Coordinators, Sponsors, Contract Research Organizations, and employees of Hackensack Meridian Health. Qualifications: Education, Knowledge, Skills and Abilities Required : BA/BS diploma/degree in science or healthcare field OR minimum of 2 or more years of experience in a related area with High School diploma, general equivalency diploma (GED), and/or GED equivalent programs.

11 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 Research Nurse Hackensack University Medical Center

Paramus, NJ

The Clinical Research Nurse is responsible for coordinating and overseeing clinical research operations for all assigned clinical trials and participates in assessing, planning, implementing and evaluating Compliant Patient Care in clinical research trials. The Clinical Research Nurse carries out the research and works under the general supervision of the principal investigator responsible for the clinical trials.

30+ 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 Coordinator Actalent Inc

Paramus, NJ

$35–$40 / hour

The coordinator supports feasibility assessment, protocol implementation, subject enrollment, data integrity, and financial compliance, contributing directly to high-quality patient care and successful research outcomes. Working under the general supervision of the principal investigator, this role serves as a central liaison among investigators, clinical research nurses, regulatory specialists, sponsors, and study participants.

5 days ago

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Clinical Jobs in Ridgefield, CT

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

Clinical Director Mitchell Martin

Associate Director, Clinical Development Trial Lead (CDTL) Joulé

Clinical Lab Assistant Joulé

Dialysis Clinical Coordinator, Home Therapy U.S. Renal Care

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

Clinical Research Coordinator - Clinical Research Department - Poughkeepsie, NY Northwell Health

Senior Clinical Study Manager Integrated Resources, Inc

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

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

Senior Clinical Data Manager Integrated Resources, Inc

Clinical Data Manager Integrated Resources, Inc

Clinical Research Coordinator - Clinical Research department in Poughkeepsie, NY Nuvance Health

Clinical Research Scientist Integrated Resources, Inc

Clinical Research Nurse 2 Yale University

Clinical Research Associate I Stony Brook University

Clinical Research Nurse Actalent Inc

RN Pediatric Clinical Research - PRN Act for Health

Clinical Research Assistant Stony Brook University

Clinical Research Coordinator Hackensack Meridian Health

Clinical Program Manager Integrated Resources, Inc

Remote Clinical Research Specialist Integrated Resources, Inc

Clinical Research Coordinator-Full-time-Onsite Holy Name Medical Center

Director of Administration, Cancer Clinical Trials Office Stony Brook University

Director Of Administration, Cancer Clinical Trials Office Stony Brook University

Clinical Research Nurse Hackensack Meridian Health

Clinical Research Specialist Integrated Resources, Inc

Manager, Clinical Study Lead Regeneron Pharmaceuticals Inc

Manager Clinical Study Lead Regeneron Pharmaceuticals Inc

Cancer Clinical Trials Finance Manager Stony Brook University

Senior Manager Clinical Study Inspection Readiness Regeneron Pharmaceuticals Inc

Clinical Research Associate, Sponsor Dedicated IQVIA Holdings Inc

RN Clinical Research Hartford HealthCare Corp

Senior Trauma Clinical Data Coordinator - Full Time - Day Hackensack University Medical Center

Clinical Research Coordinator New York Medical College

Clinical Research Coordinator Lead Nuvance Health

Senior Clinical Data Manager Celldex Therapeutics Inc

Clinical Data Coordinator Hackensack Meridian Health

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

Ycci Clinical Research Nurse 2 Yale University

YCCI Clinical Research Nurse 2 Yale University

Clinical Research Nurse 1 Yale University

Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLP

Clinical Research Nurse Hackensack University Medical Center

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

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

Clinical Research Coordinator Actalent Inc

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