Clinical Research Monitor(CRA) LanceSoft IncClinical Research Monitor(CRA)Virtual, CO$70–$75 / hourEnjoy the convenience of working remotely while having the opportunity to travel extensively across the United States, supporting groundbreaking clinical trials. Responsibilities: Monitor the progress of clinical trials at site level or headquarters, ensuring compliance with protocols, SOPs, GCP, and regulatory requirements.
Senior Clinical Research Project Coordinator - Denver Medpace, Inc.Senior Clinical Research Project Coordinator - DenverDenver, ColoradoFull timeResponsibilities: Engage in clinical trial management on a day to day level; Work closely with the project CTM for timely delivery of tasks consistently with a high degree of accuracy; Compile and maintain project-specific status reports; Interact with the Sponsor, study sites, and internal associates; Provide oversight and quality control of our internal regulatory filing system; Manage study supplies; Create and maintain project timelines; and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Clinical Trials Post-Award Specialist (Research Services Post Award Principal Professional) University of ColoradoClinical Trials Post-Award Specialist (Research Services Post Award Principal Professional)Denver, CO$67,864–$90,937 / yearThe incumbent provides comprehensive post-award management from award setup through project closeout, including financial reconciliation, invoicing, clinical trial revenue management, study budget monitoring, payroll expense transfers, effort reporting, subaward administration, and financial reporting. The campus is a state of the art medical campus home to the University of Colorado Schools of Medicine, Nursing, Dentistry, Pharmacy, the Colorado School of Public Health; as well as the University of Colorado Hospital and Children''s Hospital Colorado both of which serve as major training sites for the Denver Health Residency in Emergency Medicine.
Clinical Team Lead (Oncology) Flourish ResearchClinical Team Lead (Oncology)Denver, ColoradoProvide pertinent communications (written and oral) of sufficient frequency to effectively disseminate information and/or to gain feedback regarding the team’s performance and any issues requiring intervention/management; Participate in the start-up and oversee and supervise the conduct and close out of studies assigned to the team; Provide quality control review of participant/patient charts prior to randomization or screen fail to ensure accuracy of status determination; Provide close oversight and review of data collection, data entry as well as protection of data integrity for all studies assigned to the team; Ensure data integrity for all work performed by assigned team members through close oversight and review of source document creation and utilization in the study, of data collection and timely data entry procedures, and by performing quality control reviews of completed work; Assist with oversight of team members to the degree necessary by reviewing/monitoring study-specific logs, internal queries, RealTime CTMS entries, monitoring visit reports/follow-up letters, and by interfacing with sponsor/CRO representatives; Ensure assigned team maintains sufficient supply of lab kits and other study specific supplies; oversee the maintenance of kit storage area to maintain valid kits and disposing of expired materials per sponsor and/or Company policy/protocol. Represent Flourish in a professional and courteous manner (verbal, written and in appearance) when interacting with staff, sponsors/CROs, IRBs, patients/subjects, nursing and medical staff members of various clinics, hospitals and physicians’ offices; Ensure the maintenance of confidentiality by team members of participant/patient information as appropriate and as bound by Confidentiality Agreements between Flourish Research and sponsors/CROs and other entities while abiding by HIPAA regulations; As needed, performs duties as specified in line with a Senior CRC; Coordinate multiple and complex protocols while providing guidance of day-to-day activities of the team; Follow and ensure compliance with SOPs by team members for assigned team; Assist in the review, development, and implementation of SOPs; Assists with evaluating and leading the conduct of studies including accurate and timely entry into EMR, EDC, CTMS, and other systems as required; Provides feedback to Site Director on team and organizational performance; May assist and provide input to Site Director with hiring, performance management, talent planning, and termination decisions; Educate, mentor and provide orientation and ongoing training for Clinical Research staff to ensure qualified personnel.
Clinical Research Patient Coordinator Rocky Mountain Cancer CentersClinical Research Patient CoordinatorBoulder, Colorado$60,000–$75,000 / yearOverview: Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Patient Coordinator/RN in Boulder. Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medical, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials and GCP concepts.
Clinical Research Coordinator/RN Rocky Mountain Cancer CentersClinical Research Coordinator/RNLongmont, Colorado$60,000–$75,000 / yearKnowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medical, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, clinical trials and GCP concepts. Overview: Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Clinical Research Coordinator/RN in Longmont.
Clinical Research Coordinator CenExelClinical Research CoordinatorEnglewood, ColoradoRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Clinical Research Coordinator (Open Rank) University of ColoradoClinical Research Coordinator (Open Rank)Aurora, CO$54,302–$72,765 / yearIf you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. Job Summary: As an important member of the IBD research team, the Clinical Research Coordinator (Intermediate or Senior) supports the implementation and coordination of clinical research programs conducted by Dr. Mark Gerich and colleagues at the University of Colorado.
Prin Clinical Research Spec Medtronic PlcPrin Clinical Research SpecLafayette, COThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Senior Clinical Research Associate IRESenior Clinical Research AssociateDenver, Colorado$110,520–$138,150 / yearPerform remote and on-sitemonitoring/co-monitoringvisits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. Senior Clinical Research Associate - Oncology Phase I - Denver, CO ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Sr. Clinical Operations Manager CPC Clinical ResearchSr. Clinical Operations ManagerAurora, CO$95,045–$118,806 / yearProvide expert advice in the design, writing and/or review of all project-related essential documents including protocols, project management plans, case report forms, statistical analysis plans, project management plans, ICF templates, study procedure manuals, source documents, site newsletters, study reports, resource tools, monitoring plans and report templates. Endpoint and Specialty Services Responsibilities: Define and monitor Endpoint and Specialty Services scope, timelines and deliverables from project initiation to closeout with assistance from study assigned Clinical Operations Manager and the Head of Endpoint and Specialty Services.
Open Rank Research Services Clinical Sciences Professional (Entry to Senior) University of ColoradoOpen Rank Research Services Clinical Sciences Professional (Entry to Senior)Aurora, CO$49,899–$66,865 / yearJob Summary: The Research Services Clinical Sciences (Open Rank - Intermediate to Senior) Professional provides essential support to the Pathology Shared Resource by coordinating the collection, processing, storage, and management of biospecimens for clinical and translational research. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively.
Senior Financial Analyst, Grants Administration (Clinical Trials Services) Denver Health and Hospital AuthoritySenior Financial Analyst, Grants Administration (Clinical Trials Services)Denver, ColoradoThe Senior Financial Analyst, Grants Administration is responsible for managing contracts, grants, cooperative agreements, confidentiality agreements, data use agreements, other outside funding activities, and assigned projects including sponsor and grant deliverables. Participates in the development of grant applications and grant budgets, coordination of grant proposal development and submission, and assisting scientists, investigators, program/project managers, and directors with grant award processing.
Clinical Informatics Analyst Medpace, Inc.Clinical Informatics AnalystDenver, ColoradoFull timeBachelor’s in informatics, computer science/engineering, biomedical engineering, health information, statistics, or related field; Analytical thinker with great attention to detail; Ability to prioritize multiple projects on a sprint schedule; Excellent verbal communication skills; Programming experience in R or Python; Work experience with clinical data; Experience building web applications is preferred (with either Shiny or Streamlit); and. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Vice Chair Of Clinical Operations University of ColoradoVice Chair Of Clinical OperationsAurora, CO$500,000–$650,000 / yearThe campus encompasses the University of Colorado health professional schools, more than 60 centers and institutes, and two nationally ranked independent hospitals- UCHealth University of Colorado Hospital and Children's Hospital Colorado - that treat more than two million adult and pediatric patients each year. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively.
NewClinical Research and Regulatory Affairs Specialist University of ColoradoClinical Research and Regulatory Affairs SpecialistDenver, CO$71,517–$95,833 / yearJob Summary: The Gates Institute at the University of Colorado Anschutz seeks a highly motivated, detail-oriented Clinical Research and Regulatory Affairs Specialist to support the product and clinical safety lifecycle starting at the preclinical development stage through first-in-human (FIH) Phase I clinical trials through safety monitoring & risk assessment, regulatory compliance & documentation, data integrity & quality control, and process optimization. Key Responsibilities: Regulatory Operations: Coordinate regulatory activities supporting investigator-initiated cell and gene therapy (CGT) programs from preclinical development through first-in-human (FIH) Phase I clinical trials, including preparation and submission of IND applications, protocol amendments, annual reports, and other regulatory documentation.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedCOTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceCOTogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Clinical Research Coordinator Quicksilver Scientific, IncClinical Research CoordinatorLouisville, COFull timeAs we continue to expand our scientific research initiatives, we're looking for a Clinical Research Coordinator who is organized, analytical, and excited to play a key role in bringing high-quality clinical research to life. What You'll DoAs our Clinical Research Coordinator, you'll oversee the planning, coordination, and execution of clinical research studies that support product innovation, scientific validation, and educational initiatives.
Clinical Nurse Manager - RN Required Healogics IncClinical Nurse Manager - RN RequiredLakewood, CO$87,200–$117,500 / yearOrganizes and prioritizes clinical responsibilities, provides clinical oversight to clinical staff, such as Registered Nurses (RNs); Licensed 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.