Club Grand Reopening - Fitness Manager 24 Hour Fitness USA IncClub Grand Reopening - Fitness ManagerPearl City, HI$21.74–$26.57 / hourGrow fitness revenue by effectively gaining, training and retaining personal training and group training clients personally as well as through the club staff, in particular the personal trainers and sales team. The FM leads by example with personal sales of fitness products and develops all team members at the club to effectively communicate and build value in fitness programs and services to guests and members.
Clinical Research Coordinator American Oncology NetworkClinical Research CoordinatorHot Springs, Arkansas$53,040–$93,267.20 / yearThe Clinical Research Coordinator is involved in multiple aspects of the research process under the general supervision of the Clinical Research Manager and the Research Director. Responsible for supporting study feasibility, regulatory submissions, and study initiation activities to ensure compliance with protocols, regulatory requirements, and institutional policies.
NewSenior Clinical Research Associate Be The MatchSenior Clinical Research AssociateMinneapolis, MNFull timeAdditionally, this position is responsible for coordinating and providing support for all aspects of the study including protocol and site management, development and management of study metrics, providing training and mentorship to junior team members, and demonstrates advanced knowledge of monitoring functions. • Performs and oversees study tracking (e.g., CTMS, start-up, milestone, closeout); generates, reviews, and distributes management reports from internal tracking systems proactively and at requested intervals.
Quality Assurance Coordinator (Clinical Research) CenExelQuality Assurance Coordinator (Clinical Research)Hollywood, FloridaGCP, and ICH guidelines; Able to take a flexible approach to shifting priorities; Able to manage multiple projects and responsibilities; Motivated to work consistently in a fast paced and rapidly changing environment; Must be detail oriented and have exceptional computer, organizational, and communication skills – both written and oral. Performs ongoing review of a percentage sampling of study inclusion/exclusion, study procedure records, and laboratory reports to ensure that they are conducted according to the protocol, applicable SOPs, ICH/GCP guidelines and federal regulations.
NewClinical Research Data Specialist I University of Southern CaliforniaClinical Research Data Specialist ILos Angeles, CaliforniaWhen extending an offer of employment, the University of Southern California considers factors such as (but not limited to) the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations. This position supports one of the nation's premier urologic oncology research programs by managing high-quality clinical research data that drive scientific discovery, translational research, and improvements in patient care.
Clinical Research QA Specialist - Pulmonary Cincinnati Children’s HospitalClinical Research QA Specialist - PulmonaryPrepare and execute monitoring plans both internally and at affiliate sites, including site visits to ensure protocol and regulatory compliance; data management tasks to ensure study data integrity; verify essential documents are accurate, complete, and maintained; and coordination of applicable follow-up activities. Monitoring - Develop comprehensive data safety monitoring plans for all clinical trial activities within the assigned department to ensure that trials are conducted in compliance with the protocol, SOPs, ICH GCP, federal, state, and local regulatory requirements.
Exercise Specialist, Fitness Healthworks WakeMed Health & HospitalsExercise Specialist, Fitness HealthworksRaleigh, North CarolinaLicensure: Certified Clinical Exercise Physiologist Required - Or Certified Exercise Physiologist Required - Or Certified Medical Exercise Specialist Required Education: Bachelor's Degree Required Experience: 1 Year Fitness or Other Clinical Exercise Required Overview: The Fitness & Wellness Exercise Specialist provides exercise programming, prescription, and exercise therapy for the individuals with medical conditions requiring participation in a clinical setting.
Medical Assistant (Clinical Research) CenExelMedical Assistant (Clinical Research)Hollywood, FloridaWith moderate oversight, the Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials.
Sports Safety Educator Hospital for Special SurgerySports Safety EducatorWest Palm Beach, FLThe Athlete Health Per Diem Educator will provide public health-based education to athletes, coaches, parents, teachers and administrators as part of the Athlete Health Program at Hospital for Special Surgery. Specific job responsibilities include (but are not limited to): Deliver educational workshops and neuromuscular training sessions for and other partner organizations under the direction of the HSS Athlete Health Program Manager.
Lead Clinical Research Associate Alira HealthLead Clinical Research AssociateBoston, MassachusettsLead CRAs work closely with US: Director of Clinical Monitoring, In-house CRAs, field CRAs, EU: Associate Director of Clinical Monitoring, CRAs, CTCs and Clinical Project Managers to ensure protocol compliance, address site questions, and assist with study recruitment, site training, and other site-related issues. Prepares consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status.
Virtual Social Worker RelodeVirtual Social WorkerIllinoisYou will be responsible for assessing patients behavioral health , developing/managing a personalized care plan tailored to their specific behavioral health needs, and coordinating their care across Our Companys and the Health Systems care team. You will be a part of an integrated team of clinical professionals including Nurse Practitioners and Clinical Exercise Physiologists working together to deliver a world-class patient experience.
Miami, FL- Clinical Research Coordinator Actalent IncMiami, FL- Clinical Research CoordinatorMiami, FL$25–$32 / hourIf you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options. You will need to perform effective communication about the clinical trial, spread study awareness in the community, and conduct patient-centered research activities.
Licensed Vocational Nurse - Clinical Research (Friday, Saturday, Sunday) CenExelLicensed Vocational Nurse - Clinical Research (Friday, Saturday, Sunday)Los Alamitos, CaliforniaProvides general nursing care to study participants as necessary; including, but not limited to monitoring of vitals, blood sugar, vital signs, lab tests, etc. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology.
Clinical Research Physician - Internal Medicine (Part time) Alcanza Clinical ResearchClinical Research Physician - Internal Medicine (Part time)Kansas City, MOEssential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes. The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
Clinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) Preferred West Cancer CenterClinical Research Coordinator- Phase II-III - Full-Time - Wolf River - Registered Nurse (RN) PreferredGermantown, TNThe Clinical Research Coordinator plays a vital role in managing oncology patients participating in pharmaceutical-sponsored clinical trials. If you are a detail-oriented clinical research professional looking to make a difference in oncology care, apply today to become a Clinical Research Coordinator at West Cancer Center.
NewAssociate Clinical Research Coordinator IREAssociate Clinical Research CoordinatorDowners Grove, Illinois$38,728–$48,410 / yearAssociate Clinical Research Coordinator - Lisle, IL (Onsite, multiple locations) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Complete training on Clinical Trial Management System and maintain skills to update the database, complete participant reimbursement, capture referral source of participants, and create call lists to promote recruitment.
Clinical Research Registered Nurse Alcanza Clinical Research LLCClinical Research Registered NurseOrlando, FLRequesting and tracking medical record requests; Updating and maintaining logs, chart filings; Maintaining & ordering study specific supplies; Scheduling subjects for study visits and conducts appointment reminders; Building/updating source as needed; Conducting monitoring visits and resolves issues as needed in a timely manner; Ensuring study related reports and patient results are reviewed by investigator in a timely manner; o Filing SAE/Deviation reports to Sponsor and IRB as needed; o Documenting and reporting adverse events; o Reporting non-compliance to appropriate staff in timely manner; o Maintaining positive and effective communication with clients and team members; o Always practicing ALCOAC principles with all documentation; Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study; Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc. Responsibilities may include but are not limited to: Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: Screening of patients for study enrollment; Patient consents; Patient follow-up visits; Documenting in source clinic charts; Entering data in EDC and answers queries; Obtaining vital signs and ECGs; May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up; Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc.
Clinical Research Assistant B University of PennsylvaniaClinical Research Assistant BPhiladelphia, PA$19.47–$19.81 / hourLong-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning.
Houston, TX FT- Clinical Research Coordinator Actalent IncHouston, TX FT- Clinical Research CoordinatorHouston, TX$25–$35 / hourWe are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Clinical Research Coordinator II - Psychiatry Tufts MedicineClinical Research Coordinator II - PsychiatryBoston, MA$47,924.24–$59,894.75 / yearClinical Research Coordinator II - Psychiatry: This position will assist the Principal Investigator (PI) in the planning, implementation, and coordination of clinical research studies focused on neuropsychiatric and neurodegenerative disorders, including studies involving cognitive and psychiatric assessment, biomarker collection, digital health technologies, EEG, and home-based noninvasive brain stimulation interventions, including tDCS and tACS. The Clinical Research Coordinator II will support participant recruitment, study operations, data collection, regulatory compliance, and participant retention across clinic-based and remote research settings, including administration of cognitive, behavioral, functional, and patient-reported outcome measures, as well as support for device setup, remote monitoring, adherence tracking, and troubleshooting.