Clinical Research Regulatory Coordinator I University of Alabama at BirminghamClinical Research Regulatory Coordinator IUniversity, MS$18.85–$24.50 / hourResponsibilities also include assisting with documentation oversight (regulatory binders, eISFs, logs, etc.), ensuring all documents meet ICH-GCP, FDA, OHRP, and UAB policies, and compliance monitoring (must be knowledgeable of or willing to learn federal regulations, human subjects protections, HIPAA, and informed consent processes). Must possess great computer skills, have experience with Microsoft Office, be able to engage in group meetings and discussions, be able to actively work closely with others and under the leadership of Investigators and senior research coordinators in a variety of settings, and have a strong work ethic.
Clinical Research Coord 3, MCVI Research, FT, 8A-4:30P Baptist Health South Florida IncClinical Research Coord 3, MCVI Research, FT, 8A-4:30PMiami, FL$32.12–$41.76 / hourOur approach is rooted in a "grow our own" philosophy, designed to help our team members build meaningful, long-term careers with us, supported by benefits that make a real difference, including: Career growth and development opportunities, with clear pathways and ongoing support. Baptist Health is the region''s largest not-for-profit healthcare organization, with 12 hospitals, over 29,000 employees, 4,500 physicians and 200 outpatient centers, urgent care facilities and physician practices across Miami-Dade, Monroe, Broward and Palm Beach counties.
Clinical Research Associate Macpower Digital Assets Edge Private LimitedClinical Research AssociateResearch Triangle Park, NC$95–$105 / hourCommunicates and interacts with relevant study personnel, including developing and maintaining collaborative relationships to manage study issues and support milestone achievement; conveys project information; answers study questions in a timely manner while using discretion when to escalate to the study manager; troubleshoots and follows up on study progress; and reviews report data for completeness and accuracy. Prepares telephone contact reports, confirmation letters, site visit reports (PSV, SIV, IMV, and COV), and follow-up letters to accurately and completely document site status and activities.
RN Clinical Nurse II (Per Diem)- GI Surgery & Surgical Oncology Acute Care Unit UNC HealthRN Clinical Nurse II (Per Diem)- GI Surgery & Surgical Oncology Acute Care UnitChapel Hill, NC$33.88–$47.91 / hourOur patient populations require close post-operative observation, occasional remote cardiac telemetry, early aggressive mobilization, pulmonary hygiene, extensive physical therapies, IV, central line/PICC line care, administration of TPN, anticoagulation, oxygen therapy, pain management, blood product administration, intake/output and ostomy care. Our interdisciplinary team provides evidence-based and high-quality care primarily to adult post-surgical patients with weight loss issue, gastrointestinal (GI) cancers, and complex non-cancer GI-related illnesses.
Clinical Research Associate Allen SpoldenClinical Research AssociateNew York, New JerseyConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Associate II Allen SpoldenClinical Research Associate IIPansey, AlabamaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Associate 1 Allen SpoldenClinical Research Associate 1Seattle, WashingtonConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
Clinical Research Associate (All levels) - North East, USA Evestia ClinicalClinical Research Associate (All levels) - North East, USAFloridaEvestia Clinical is looking Clinical Research Associate (II or Senior), in the North East, to be responsible for ensuring that the rights and safety of clinical trial participants are protected and that the clinical data obtained are accurate, complete, and verifiable according to source. We partner with clients to provide expert guidance through complex clinical trials in specialized areas, including Rare Disease, Oncology, Neurology, and Immunology.
Clinical Research Associate (All levels) - South East, USA Evestia ClinicalClinical Research Associate (All levels) - South East, USAWashington State, WashingtonEvestia Clinical is looking Clinical Research Associate (II or Senior) in the North West to be responsible for ensuring that the rights and safety of clinical trial participants are protected and that the clinical data obtained are accurate, complete, and verifiable according to source. We partner with clients to provide expert guidance through complex clinical trials in specialized areas, including Rare Disease, Oncology, Neurology, and Immunology.
Senior Clinical Research Associate Ergomed Group LtdSenior Clinical Research AssociateRaleigh, NCAcross the Group, our teams turn the signals that clinical trials, safety systems and quality data generate into insight that helps bring safer treatments to patients around the world. Performs on-site or remote Pre-Study, Initiation, Interim, and Close-Out monitoring visit activities to ensure that facilities and staff at the investigational site continue to be adequate for the conduct of the study.
Clinical Research Assistant Temple UniversityClinical Research AssistantPhiladelphia, Pennsylvania$45,000The Clinical Research Assistant works under the direct supervision of the Principal Investigator and/or other Research Coordinators and will assist with specific research tasks associated with clinical research projects or clinical trials. With access to advanced resources, collaborative teams, and a strong commitment to excellence, Temple offers an ideal environment for Clinical Research Coordinators to grow their careers while shaping the future of medicine.
NewClinical Chemistry Pathology position at UPMC Presbyterian in Pittsburgh, PA UPMC Southwestern PAClinical Chemistry Pathology position at UPMC Presbyterian in Pittsburgh, PABrentwood, PAExperience working in a large hospital-based clinical chemistry laboratory that provides technical directorship in general chemistry, urinalysis, toxicology, therapeutic drug monitoring, immunopathology, and esoteric testing is beneficial, together with a proven academic track record of effective communication (written, verbal and presentation). The city is renowned for its cultural institutions, including the Carnegie Museums of Pittsburgh, Pittsburgh Parks Conservancy, Pittsburgh Zoo & Aquarium, Phipps Conservatory and Botanical Gardens, the National Aviary, and a diverse cultural district.
Clinical Program Manager, Oncology Research (NP or RN Required) - Tisch Cancer Center Mount Sinai Health SystemClinical Program Manager, Oncology Research (NP or RN Required) - Tisch Cancer CenterNew York, NY$115,494–$192,328 / yearMount Sinai advances health for all people, everywhere, by taking on the most complex health care challenges of our time - discovering and applying new scientific learning and knowledge; developing safer, more effective treatments; educating the next generation of medical leaders and innovators; and supporting local communities by delivering high-quality care to all who need it. We are consistently ranked by U.S. News & World Report's Best Hospitals, receiving high "Honor Roll" status, and are highly ranked: No. 1 in Geriatrics, top 5 in Cardiology/Heart Surgery, and top 20 in Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology.
Research Infusion Nurse I - Oncology Washington University in St LouisResearch Infusion Nurse I - OncologySt. Louis, MO$30.38–$52.83 / hourSkills: Chemotherapy Infusion, Clinical Trial Planning, Constructive Feedback, General Nursing, Group Problem Solving, Individualized Treatment Planning, Interpersonal Relationships, Nursing Practice, Oncology Nursing, Oncology Research, Patient Care, Patient Charting, Professional Etiquette, Protocol Implementation, Research Data Collection, Site Supervision. Coordinates with the treating team, investigational pharmacy, clinical pharmacists, infusion nursing, clinical research coordinators, protocol content administration team and other required departments to assist in constructing and executing an appropriate plan of care for each research patient.
Pediatric Nurse Practitioner or Physician Assistant, Research NemoursPediatric Nurse Practitioner or Physician Assistant, ResearchWilmington, DEFull timeThe incumbent will coordinate, implement and complete clinical research studies or clinical trials by assisting with IRB submissions, assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent, educating parents/participants, scheduling and conducting study procedures/examinations, collecting and recording study data, maintaining study records, interfacing with study sponsors, participation in sponsor study monitoring visits. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
NewAssociate Attorney - Tampa CAN Community HealthAssociate Attorney - TampaTampa, FL$112,804–$141,005 / yearThe practice includes significant work involving healthcare transactions, academic medicine, clinical research, and the use and commercialization of health data. The associate will advise healthcare stakeholders on a wide range of corporate, transactional, regulatory, and operational matters.
Sr. Clinical Research Associate, IQVIA IQVIASr. Clinical Research Associate, IQVIADurham, KansasEnsure 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.
Clinical Research Coordinator I - Emergency Medicine Nationwide Children's HospitalClinical Research Coordinator I - Emergency MedicineColumbus, OHFREQUENTLY: Bend/twist, Biohazard waste, Blood and/or Bodily Fluids, Chemicals/Medications, Communicable Diseases and/or Pathogens, Lifting / Carrying: 0-10 lbs, Lifting / Carrying: 11-20 lbs, Lifting / Carrying: 21-40 lbs, Machinery, Patient Equipment, Pushing / Pulling: 0-25 lbs, Pushing / Pulling: 26-40 lbs, Pushing / Pulling: 41-60 lbs, Pushing / Pulling: 61-100 lbs, Sitting, Standing, Walking. CONTINUOUSLY: Audible speech, Computer skills, Decision Making, Depth perception, Flexing/extending of neck, Hand use: grasping, gripping, turning, Hearing acuity, Interpreting Data, Peripheral vision, Problem solving, Repetitive hand/arm use, Seeing - Far/near.
Research Coordinator III - Academic Offices of Clinical Trials Houston MethodistResearch Coordinator III - Academic Offices of Clinical TrialsAt Houston Methodist, the Research Coordinator III position is responsible for coordinating the drive on multiple clinical research projects and/or for multiple Principal Investigators (PI), gathering patient data via methods specified in the study protocol and providing general administrative duties in support of the study. Houston Methodist also includes a research institute; a comprehensive residency program; international patient services; freestanding comprehensive care clinics, emergency care and imaging centers; and outpatient facilities.
Clinical Research Coordinator Medical Oncology Associates of San DiegoClinical Research CoordinatorSan Diego, CaliforniaThe Clinical Research Coordinator works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Additional duties and responsibilities: Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.