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Greater than 1 year applicable experience as a trained Histotechnician in a high complexity Histology Laboratory OR one year of Lab Support Assistant experience in a high complexity Histology laboratory followed by on the job training and demonstrated competency or other clinical experience in a hospital/healthcare clinic.
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Working in a fast-paced, high volume, dynamic environment, the Clinical Authorization Specialist will bring clinical expertise to the prior authorization and appeals processes and serve as a liaison and patient advocate between Dana Farber Cancer Institute and various health plans.
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The Mass General Hospital Division of Palliative Care & Geriatric Medicine is seeking a competent and compassionate Clinical Nurse (RN) to join the Geriatric Medicine Service. The Clinical Nurse collaborates with the Nursing Director, Medical Director, NP Team Lead, and other members of the patient care team to achieve optimal patient outcomes and practices in accordance with established institutional and departmental policies & procedures and standards of practice.
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West Newton Healthcare is seeking a Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor. Currently seeking an exceptional Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor to join our team in our West Newton Healthcare facility.
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Are you passionate about your Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor career, then look no further, come and join our great team here at West Newton Healthcare! Are you passionate about your Clinical Manager Licensed Practical Nurse (LPN) Nurse Supervisor career, then look no further, come and join our great team here at West Newton Healthcare.
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Confirm archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents. Understanding of industry standard technologies to support Clinical Development needs (e.g., CTMS, SAS, R or Python, Data Warehouses, SharePoint.
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Strong knowledge of biomarker technologies and methodologies, including genomics, proteomics, imaging, and flow cytometry, as applied to clinical research. Qualifications:Ph. D. or equivalent degree in Molecular Biology, Biochemistry, Pharmacology, or related field with a minimum of 8 years of relevant experience in clinical biomarker research within the biopharmaceutical industry.
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Head up the development team starting at the time of CTA/IND or proof of concept depending on the program, including all functions: clinical, regulatory, biostatistics, program management, clinical operations, tech ops/CMC, clinical pharmacology, research, and preclinical development, to design and execute clinical development plans for assigned projects.
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Lead or Co-lead all quantitative pharmacology activities to support both regulatory filings and internal decision-making (e.g., Exposure-Response, QTc prolongation risk assessment, population PK/PD analysis) by working closely with internal colleagues (i.e. DMPK, toxicology, biology, clinical, statistics) and external vendors to advance programs from Phase I to late-stage development.
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Examples: physicians, clinical nurses, phlebotomist, medical assistants, PFT tech, and x-ray tech. Reporting directly to the Practice Manager and Senior Director of Nursing, the Team Nurse position is responsible for performing the duties of a RN/LPN in an outpatient primary care or family medicine practice and serves as a clinical resource for the medical practice.
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Job Title: Environmental Health and Safety Specialist II (Onsite)
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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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Significant experience with EDC platforms and database design, including Medidata Rave and Oracle Clinical Inform. Reporting to the VP of Biometrics, the Director/Sr. Director, Clinical Data Management is responsible for all clinical data management activities related to the effective planning and timely delivery of complete, high quality and reliable clinical trial data.
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The Real World Evidence (RWE) lead provides clinical leadership for evidence generation activities, supporting the integration of RWE into Sarepta key strategic initiatives. The role functions in a company matrix team environment interacting with several key stakeholder groups including; Clinical Development, Pharmacovigilance, Regulatory Affairs, Quality Assurance, Manufacturing, Commercial, Medical Affairs, Research and Legal.
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The Principal Scientist, Computational Biology leads the development and deployment of computational methods for NGS-based clinical diagnostic assays in our clinical labs. Working as part of a large multidisciplinary team, this role distills the latest advances in computational methods, genomics, and oncology to develop innovative, best-in-class clinical diagnostic tools.
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histology clinical jobs in Cambridge, MA
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