Abrar Admin

Hawaii Pacific Neuroscience

Hawaii Pacific Neuroscience (HPN) is one of the largest and leading provider of neuroscience care and research in the state. Be part of the fastest growing and recognized as one of the most sought-after neuroscience clinical research site in US including an overnight phase 1 PK Unit Site specializing in phase 0, I,II,III studies with an average of 20 + studies at any one time. Join a winning team and be supported by world-class full-time neuroscience specialists including neurologists, physiatrists, geriatrician, sleep specialist supported by &gt; 50 full time dedicated happiest employees in Hawaii. Seeking Clinical Research Assistant at Clinical Research Center. Your responsibilities will be to perform clinical research in conjunction with multiple clinical research protocols and will be supervised by the Principal investigator You will play an important role as you will have direct contact with patients and create an atmosphere of trust and confidence while explaining procedures and educating them on the study. This position requires an extremely detail-oriented, well-organized individual who can multi-task and work in a fast-paced environment.Responsibilities Include:<ul><li>Reviewing patient records to determine patient eligibility for participating in research protocol.</li><li>Analyzing appropriate data for recruitment purposes and interview patients for protocol to determine patient commitment.</li><li>Responsible for completing all data entry requirements accurately including data entry of patient registration; entry of test order from requisition or pulling order from database; managing Standing Orders.</li><li>Collecting, organizing, cataloging, disseminating, and maintaining appropriate files of current patient data.</li><li>Assisting with monitoring audits/visits for clinical protocols.</li><li>Processing specimens, including labeling, centrifuging, splitting, and freezing specimens as required by test order.</li><li>Performing clerical duties when assigned such as data entry, inventory, stock supplies, and answer phones when needed.</li><li>Maintaining all appropriate phlebotomy logs in a timely manner and based on frequency, such as maintenance logs and temperature logs.</li><li>Completing training courses and keeping up to date with the certifications.</li><li>Assisting with regulatory, research or administrative compliance.</li><li>Assisting with preparation and delivery of required reports and other research documentation.</li><li>Having strong written and oral communication, interpersonal skills and attention to detail.</li><li>Working under minimal supervision and being goal oriented.</li></ul>Requirements: Bachelor&rsquo;s degree in scientific or healthcare field, 5 years of relevant experience with associate degree in scientific or healthcare field may substitute for a Bachelor&rsquo;s degree. Previous Clinical Research experience or LPN experience preferred Phlebotomy experienceCompetitive salary with full benefits including paid vacations, health, dental, 401K offered.Schedule: Monday - FridayInterested candidate to contact: Ashley BassJob Type: Full-timePay: $21.00 - $27.00 per hourBenefits:<ul><li>401(k)</li><li>Dental insurance</li><li>Employee discount</li><li>Flexible spending account</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Clinical Research Lab Assistant (Phlebotomist)

Job Overview We are seeking a dynamic and detail-oriented Clinical Research Coordinator to join our team and drive forward innovative clinical trials. In this pivotal role, you will coordinate all aspects of clinical research studies, ensuring compliance with regulatory standards, managing data collection, and maintaining seamless communication between research teams, participants, and regulatory bodies. Your energetic approach will help accelerate the development of new therapies and improve patient outcomes. This paid position offers an exciting opportunity to contribute to cutting-edge medical research in a collaborative environment dedicated to excellence.Duties<ul><li>Oversee the planning, implementation, and management of clinical trials in accordance with FDA regulations, ICH GCP guidelines, and institutional policies</li><li>Recruit, screen, and monitor study participants, ensuring adherence to protocol and safety standards</li><li>Review and verify all study documentation for accuracy, completeness, and compliance with regulatory requirements</li><li>Collect, record, and manage clinical data using electronic Medical Record (EMR) systems and adhere to CDISC standards for data formatting</li><li>Conduct patient assessments including vital signs, blood sampling (phlebotomy), and monitoring of clinical laboratory results</li><li>Supervise research staff and coordinate activities related to clinical trials management, including training on Good Clinical Practice (GCP) procedures</li><li>Ensure compliance with HIPAA regulations to protect patient privacy and confidentiality at all times</li></ul>Skills<ul><li>Proven supervising experience in clinical research settings with strong leadership capabilities</li><li>Extensive knowledge of clinical trials management processes from protocol development to data analysis</li><li>Proficiency in medical terminology, blood sampling techniques, and clinical laboratory procedures</li><li>Skilled in reviewing documentation such as consent forms, case report forms (CRFs), and regulatory submissions</li><li>Ability to monitor patients effectively while maintaining high standards of care and safety protocols</li><li>Experience with statistical software for data analysis and interpretation of trial results</li><li>Familiarity with FDA regulations, ICH GCP guidelines, HIPAA compliance, and CDISC standards for data management</li><li>Clinical laboratory experience including blood sampling techniques such as phlebotomy</li><li>Strong understanding of clinical development phases and research methodologies</li><li>Certification in GCP from a recognized issuer (such as ICH GCP certificate) or equivalent certification in Good Clinical Practice (GCP) applicable in California or other regions</li><li>Knowledge of EMR systems for efficient data entry and retrieval during trial conduct</li><li>Excellent analysis skills for interpreting complex clinical data sets accurately</li><li>Ability to manage multiple projects simultaneously while ensuring strict adherence to compliance management protocols</li></ul>Join us to be part of a passionate team dedicated to advancing medical science! Your expertise will directly impact the development of new treatments while providing invaluable support to patients participating in groundbreaking research. We value your commitment to excellence and look forward to welcoming a motivated professional eager to make a difference.Pay: $62,400.00 - $68,000.00 per yearBenefits:<ul><li>401(k)</li><li>401(k) matching</li><li>Dental insurance</li><li>Employee discount</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Professional development assistance</li><li>Retirement plan</li><li>Vision insurance</li></ul>Work Location: In person

Clinical Research Coordinator

Join Hawaii Pacific Neuroscience and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Hawaii Pacific Neuroscience

About Company

Clinical Research Lab Assistant (Phlebotomist)

Clinical Research Coordinator