FULL_TIME

FEED

YEAR

Loureiro Engineering Associates, Inc. (Loureiro) is an employee-owned (ESOP), full-service multi-disciplinary consulting firm with operations in Connecticut, Massachusetts, Rhode Island, New Hampshire, North Carolina, and Missouri. This position offers an exciting opportunity to work alongside experienced professionals who will provide formal training and mentorship, helping you grow both technically and professionally within a collaborative environment.

<p>Loureiro Engineering Associates is seeking an entry-level Civil Engineer based in the Poughkeepsie, NY area. This position offers an exciting opportunity to work alongside experienced professionals who will provide formal training and mentorship, helping you grow both technically and professionally within a collaborative environment.</p><p>At Loureiro, you won’t just work for the company, you’ll own a part of it. As a 100% employee-owned company, our Employee Stock Ownership Plan (ESOP) gives you a company-funded ownership stake that grows over time, so when we succeed, you share in the rewards.</p><h3><strong>What You’ll Do</strong></h3><ul><li><p>Design portions of civil engineering projects with growing independence</p></li><li><p>Perform engineering calculations using standard formulas and tools</p></li><li><p>Utilize engineering catalogs to specify components and materials</p></li><li><p>Instruct drafters on translating designs into completed drawings</p></li><li><p>Conduct research and prepare technical opinions or reports</p></li><li><p>Use engineering software to solve routine design problems</p></li><li><p>Support task budgeting under the supervision of a Project Manager</p></li><li><p>Follow company safety protocols and procedures</p></li><li><p>Take on increasing responsibility as experience and skills develop</p></li><li><p>Perform other related work as apparent or assigned</p></li></ul><h3><strong>Who You Are</strong></h3><ul><li><p>A curious, analytical thinker with a strong foundation in engineering principles</p></li><li><p>Someone who understands the interaction between natural topography and the built environment</p></li><li><p>A clear communicator with strong verbal and written skills</p></li><li><p>Technically competent and eager to learn</p></li><li><p>A team player who thrives in a collaborative environment</p></li><li><p>Safety-conscious and attentive to detail</p></li><li><p>Eager to grow into more independent design responsibilities</p></li></ul><h3><strong>What You Bring</strong></h3><ul><li><p>Bachelor’s degree in Civil Engineering </p></li><li><p>0–3 years of relevant experience in civil design</p></li><li><p>EIT certification <strong>preferred</strong></p></li><li><p>Proficiency in AutoCAD</p></li><li><p>Eligibility to work in the U.S.</p></li></ul><h3><strong>Physical Requirements</strong></h3><ul><li><p>Prolonged periods of sitting, standing, walking, and hiking</p></li><li><p>Ability to lift up to 50 lbs.</p></li><li><p>Manual dexterity to operate tools and equipment</p></li><li><p>Ability to work outdoors in various weather and terrain conditions</p></li><li><p>Strict adherence to safety protocols and use of personal protective equipment</p></li></ul><h3><strong>Why Loureiro?</strong></h3><p><strong>Employee Ownership, Real Impact:</strong> Through our ESOP, you gain a meaningful financial stake in the company’s success<br/><strong>Diverse Expertise:</strong> Collaborate with specialists across engineering, environmental, construction, and EH&S fields<br/><strong>Opportunity to Advance:</strong> We offer hands-on learning, mentorship, and clear career growth paths<br/><strong>People-First Culture:</strong> Join a respectful, team-oriented environment where your voice matters<br/><strong>And Of Course… Exceptional Benefits:</strong> From health coverage to financial wellness, our benefits support you in and out of work</p><p>We are committed to delivering high-quality engineering and construction solutions that make a lasting impact, and we take pride in fostering an empowering workplace. If you’re looking to take ownership of impactful work and grow your career in a supportive environment, we’d love to hear from you!</p><p><strong>Loureiro Engineering Associates, Inc. (Loureiro)</strong> is an employee-owned (ESOP), full-service multi-disciplinary consulting firm with operations in Connecticut, Massachusetts, Rhode Island, New Hampshire, North Carolina, and Missouri. Loureiro’s areas of expertise include the integration of engineering, construction, environmental health & safety, energy, and waste management services.</p><p><strong>EEO/AAP Statement:</strong><br/>Loureiro Engineering Associates Inc. is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, disability, or protected veteran status.</p><p><em>Loureiro Engineering Associates Inc. is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability or protected veteran status.</em></p><p>Powered by JazzHR</p>

Loureiro Engineering Associates, Inc.

Entry Level Civil Engineer

Budgeting

Civil Engineering

Communication Skills

Construction Engineering

Consulting

Energy Management

Engineer in Training (EIT)

Engineering

Engineering Software

Environmental Engineering

Environmental Health

Green Construction

Manual Dexterity

Mentoring

Presentation/Verbal Skills

Problem Solving Skills

Project/Program Management

Quality Engineering

Research Skills

Safety Process

Safety/Work Safety

System Integration (SI)

Team Player

Technical Research

Topography

Training/Teaching

Waste Management

Writing Skills

partner JazzHR

UNKNOWN

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.

HOUR

<p><b>Description</b></p><div>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. Northwell cares for more than three million people annually in the New York metro area, including Long Island, the Hudson Valley, Connecticut and beyond, thanks to philanthropic support from our communities. Northwell is New York State’s largest private employer with over 104,000 employees — including members of Northwell Health Physician Partners — who are working to change health care for the better.</div><div> </div><div><strong>Title:</strong> Clinical Research Coordinator - Clinical Research Department - Poughkeepsie, NY - Full time/40 hours per week, 8-hours shifts, 8:30am - 5:00pm, Monday - Friday.</div><div> </div><div><strong>Summary:  </strong>Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Responsibilities include; patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB). Coordinates studies in varied therapeutic areas including but not limited to Cardiovascular, Pulmonary, Gastroenterology, Neurology, Endocrinology, Dermatology and Rheumatology. Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations.</div><p><strong>Responsibilities:</strong></p><p>1. Screens patients for study participation e.g. reviews medical record, collaborates with medical & research staff, etc. and procures informed consent.</p><p>2. Maintains accurate and thorough documentation on all source documents and case report forms (CRFs) for each study patient. Resolves all patient queries.</p><p>3. Maintains communication with investigators/researchers, patients, internal and external collaborators (e.g. consulting physicians), sponsors, federal regulatory agencies, and other involved parties as required.</p><p>4. Participates in investigator, coordinator, or study initiation meetings accordingly. Coordinates and participates in monitoring visits/audits with regulatory agencies or sponsors.</p><p>5. Maintains current regulatory (GCP, HSR) and study specific required trainings.</p><p>6. Prepares and submits all study protocols, consent forms, and other required documents to the Institutional Review Board (IRB).</p><p>7. Educates hospital staff about protocols through in-services, written materials and one-on-one interaction, for each study and each patient, and for general marketing.</p><p>8. Demonstrates flexibility in daily routine and effectively accommodates for the needs of the job (e.g. early or late patient enrollment).</p><p>9. 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.</p><p>10. Fulfills all compliance responsibilities related to the position.</p><p>11. Maintain and Model Northwell Health Values.</p><p>12. Demonstrates regular, reliable and predictable attendance.</p><p>13. Performs other duties as required.</p><div><strong>Other Information:</strong></div><div><strong>Education and Experience Requirements: </strong></div><ul><li>Bachelor's degree or Allied Health professional degree and three years job-related experience.</li><li>Minimum 1-year clinical experience in medical field. </li><li>Prefer: Clinical Research experience</li></ul><div><strong>Minimum Knowledge, Skills and Abilities Requirements:</strong></div><ul><li>Fluency in medical terminology. </li><li>Knowledge of clinical trials, research and general medicine. Strong computer skills.</li><li>Strong attention to detail and organizational skills</li><li>Outstanding interpersonal skills</li></ul><div><strong>License, Registration, or Certification Requirements:</strong></div><ul><li>Basic Life Support current or willing to take course</li><li>Valid Driver license</li><li>Prefer: Professional research certification </li></ul><div>Salary Range: $29.65 - $55.55 hourly (Pay per years of relative experience)</div><div> </div>

Northwell Health

Clinical Research Coordinator - Clinical Research Department - Poughkeepsie, NY

Basic Life Support (BLS)

Cardiovascular

Case Report Form (CRF)

Clinical Medicine

Clinical Practices/Protocols

Clinical Research

Clinical Trial

Community Support

Computer Skills

Data Collection

Dermatology

Detail Oriented

Documentation

Driver's License

Electrocardiogram

Endocrinology

Federal Government

Federal Laws and Regulations

Gastroenterology

Healthcare

Hospital

IRB/IEC (Institutional Review Board/Independent Ethics Committee)

Informed Consent

Leadership

Medical Records

Medical Research

Medical Terminology

Medicine

Neurology

Nonprofit

Nursing

Order Picking/Packing

Organizational Skills

Outpatient Care

Patient Care

Phlebotomy

Regulations

Research Protocols

Rheumatology

Jobvite Talemetry Organic Easy Apply

<p><b>Description</b></p><div><div>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. Northwell cares for more than three million people annually in the New York metro area, including Long Island, the Hudson Valley, Connecticut and beyond, thanks to philanthropic support from our communities. Northwell is New York State’s largest private employer with over 104,000 employees - including members of Northwell Health Physician Partners - who are working to change health care for the better.</div><div> </div></div><div><strong>Title:</strong> Clinical Research Coordinator - Danbury Hospital Clinical Trials - Full time/40 hours per week, 8- hours shifts, 8:00am - 4:30pm, Monday - Friday.</div><p><strong>Summary:</strong> Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Responsibilities include; patient screening and recruitment, coordination of care of the research patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board (IRB). Coordinates studies in varied therapeutic areas including but not limited to Cardiovascular, Pulmonary, Gastroenterology, Neurology, Endocrinology, Dermatology and Rheumatology. Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporations.</p><p><strong>Responsibilities:</strong></p><p>1. Screens patients for study participation e.g. reviews medical record, collaborates with medical & research staff, etc. and procures informed consent.</p><p>2. Maintains accurate and thorough documentation on all source documents and case report forms (CRFs) for each study patient. Resolves all patient queries.</p><p>3. Maintains communication with investigators/researchers, patients, internal and external collaborators (e.g. consulting physicians), sponsors, federal regulatory agencies, and other involved parties as required.</p><p>4. Participates in investigator, coordinator, or study initiation meetings accordingly. Coordinates and participates in monitoring visits/audits with regulatory agencies or sponsors.</p><p>5. Maintains current regulatory (GCP, HSR) and study specific required trainings.</p><p>6. Prepares and submits all study protocols, consent forms, and other required documents to the Institutional Review Board (IRB).</p><p>7. Educates hospital staff about protocols through in-services, written materials and one-on-one interaction, for each study and each patient, and for general marketing.</p><p>8. Demonstrates flexibility in daily routine and effectively accommodates for the needs of the job (e.g. early or late patient enrollment).</p><p>9. 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.</p><p>10. Fulfills all compliance responsibilities related to the position.</p><p>11. Maintain and Model Nuvance Health Values.</p><p>12. Demonstrates regular, reliable and predictable attendance.</p><p>13. Performs other duties as required.</p><p><strong>Other Information:</strong></p><p><strong>Education and Experience Requirements: </strong></p><ul><li>Bachelor's degree or Allied Health professional degree and three years job-related experience.</li><li>Minimum 1-year clinical experience in medical field. </li><li>Prefer: Clinical Research experience</li></ul><p><strong>Minimum Knowledge, Skills and Abilities Requirements:</strong></p><ul><li>Fluency in medical terminology. </li><li>Knowledge of clinical trials, research and general medicine. Strong computer skills.</li><li>Strong attention to detail and organizational skills</li><li>Outstanding interpersonal skills</li></ul><p><strong>License, Registration, or Certification Requirements:</strong></p><ul><li>Basic Life Support current or willing to take course</li><li>Valid Driver license</li><li>Prefer: Professional research certification </li></ul><p>Salary Range: $29.65 - $55.55 hourly (Pay per years of relative experience)</p><div> </div>

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

Entry Level Research Jobs in Franklin D Roosevelt, NY

Entry Level Research Jobs in Franklin D Roosevelt, NY

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Entry Level Research Jobs in Franklin D Roosevelt, NY

Entry Level Civil Engineer Loureiro Engineering Associates, Inc.

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

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

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