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Reporting to the Senior Director, Clinical Trials Office, the Associate Director, Clinical Trials Operations is responsible for the overall management and oversight of the assigned Clinical Research Disease group managers.
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Working closely with the VP and CCA leadership, the Clinical Operations Manager designs, implements and manages projects, workstreams, and specialized programs within the Advanced Practice Clinician (APC) Collaborative.
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The Oncology Clinical Trials Operations Pharmacist is principally involved with order verification and dispensing of investigational agents, and serving as a resource for Oncology Clinical Trials, Pharmacy, and MGH Cancer Center staff.
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With the assistance of the Laboratory Director and input from each lab supervisor is responsible for developing the annual Clinical Laboratory Operational and Capital budgets. Under the direction of the Administrative Director of Laboratory Services, the Clinical Laboratory Operations Manager is primarily responsible for departmental operations to assure maximum efficiency.
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Assists with recruiting patients for clinical trials. The Clinical Research Coordinator I role is tasked with coordinating clinical research studies focused on better understanding neural mechanisms involved in anesthesia, Alzheimer's disease (AD), and sleep.
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The Clinical Research Coordinator will work under the supervision of the Principal Investigator and Program Manager. Job Description - Clinical Research Coordinator II (3269300) Clinical Research Coordinator II - ( 3269300.
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Clinical experience in one following specialties or similar specialties such as: Nursing (RN/BSN/MSN), Physician Assistant (PC), CV Sonography (RDCS/RDS), Cardiovascular Technician (RCIS/CVT/RTR/RCES/CST.
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Works closely with the Clinical Director, Associate Director, and Administrative Manager for Procedural Services to ensure the highest competent nursing care is provided for all patients. The Clinical Nurse Manager (CNM) is accountable for excellence in patient care delivery, facilitating operational efficiencies, and compliance with hospital and regulatory policies and practices.
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The Research Informatics Operations (RIO) Director, Account Services for Clinical Trials Research will work closely with Dana-Farber clinical research stakeholders and functional leaders within I&A to identify, prioritize, and address the clinical research data informatics needs of DFCI.
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Provide on-going clinical support to participants and staff in specialized programs as needed, providing on-going staff support using modalities such as MI, TIC, CBT, hoarding, solution-focused, harm reduction.
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PhD or PharmD with relevant expertise in clinical pharmacology or pharmaceutical science is required. This position will work in close collaboration with different functions, including preclinical toxicology, preclinical pharmacokinetics, translational medicine, clinical, operations, and regulatory affairs.
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Location: Boston Clinical Trials | Roslindale, MA. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.
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The CRC will work within the Neuroimaging of Mind-Body Interaction and Treatment Laboratory ( The objective of the lab is to investigate the interaction between the brain (mind) and body using fMRI, EEG, MEG, and clinical assessments, and translate the findings into clinical practice.
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Has a demonstrated understanding of clinical data capture/management systems, clinical databases, data flow, and related infrastructure, with experience in/around EDC, EHR, e COA, IRT, CDR, MDR, SCE and adjacent systems.
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Thorough knowledge and understanding of standards development processes, focused on clinical data with a strong knowledge of CDISC, HL7, OMOP, ICH, ISO standards and an understanding of global privacy regulations.
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Title: clinical trials Company: Parexel in Newton, MA
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