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We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida.
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Assist with Otsuka's clinical trials program, including registrational, post-marketing and Investigator-Sponsored Trials (ISTs), health economic outcomes research, other specific medical collaborations; provide clinical expertise and feedback regarding operational management of clinical trials to ensure optimal site selection and performance.
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Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up.
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Minimum 4+ years’ experience in programming clinical trials in EDC in systems such as Veeva CDMS, RAVE, Inform, Zelta, Medrio, etc. You will work with Takeda study teams to develop eCRF specifications, build and/or oversee implementation of Case Report Forms (eCRFs) for clinical trials in EDC. The EDC Engineer will manage and oversee EDC system configuration, dictionaries, and user administration.
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Familiarity with research activities, including involvement in clinical trials, CAR-T cell therapy, and Stem Cell Transplantation. Participate in research activities, including clinical trials, and assist with the coordination of innovative therapies such as CAR-T cell therapy and Stem Cell Transplantation.
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Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills. Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role.
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ResponsibilitiesA day in the life of a Clinical Research Nurse at Hackensack Meridian Health may include:Assists the principal investigator in the preparation of proposed clinical trials by reviewing trial protocol, contacting each department who will provide resources during study and ensuring appropriate departments are notified and given a copy of proposed trial, scientific merit and accrual potential.
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They offer a range of services, including analytical and bioanalytical testing, drug discovery, preclinical studies, and late phase clinical trials. Collaboration: Work closely with cross-functional teams to support drug discovery, preclinical studies, and late-phase clinical trials.
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Collaborates with the Dana-Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific materials. Clinical:Coordinates study enrollment, protocol treatment, and completion of study requirements for patients participating in clinical trials.
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Located just 30 minutes from the beach, TidalHealth offers the widest array of specialty and subspecialty services such as neurosurgery, cardiothoracic surgery, joint replacement, emergency/trauma care, comprehensive cancer care, wound care and clinical trials and research.
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Minimum of 2 years of clinical experience as an RN, with a preference for experience in oncology nursing. Competency in performing and assisting with various medical procedures, including Chest Tube Set-up/Care, CPAP/BiPAP, Procedure Sedation, Trach Care, Blood/Blood Products Administration, Cooling/Warming Blanket, Drains, Feeding Tubes, Fistula Management, PCA Pumps, PICC/Central Lines, Port-Cath/Vascular Device Access/Care, Syringe Pumps, and Wound Vac.
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Multidisciplinary programs in Neuromuscular Medicine (EMG/NCV lab), Tuberous Sclerosis Complex Clinic, Ketogenic Diet Clinic, Neurofibromatosis Clinic, CMT Center of Excellence, PPMD-certified muscular dystrophy clinic and a close tie to the MDA.High quality academic and clinical program with ongoing clinical trials.
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Ability to participate in Graduate Medical Education and clinical research trials. Open to J1/H1B visa sponsorship. Onsite laboratory, including serology, imaging (X-Ray, MRI, Bone Density & Ultrasound), Health Psychology and Physical Therapy.
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Assist with completion of initial IRB submissions, annual continuing reviews, amendments, and reliance agreements for clinical trials• Prepare FDA submissions (1572, IND, IDE, HUD etc.) Ensure patient safety is a top priority in conducting clinical trials.
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Meets requirements of Clinical Trials Chemotherapy Nurse 50% Abides by requirements in accordance with the Oncology Nursing Society's Manual for Clinical Trials Nursing. Follow policies and procedures for clinical trials.
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clinical trials jobs Title: coordinator Company: University Of California
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