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The Clinical Data Analyst partners cross functionally to identify risk to data integrity throughout the data flow to drive quality collection for non-EDC data sources (fluid & tissue labs, digital, imaging, wearables) in Dyne's clinical studies.
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The company has approved medicines that treat the underlying causes of multiple chronic, life-shortening genetic diseases — cystic fibrosis, sickle cell disease and transfusion-dependent beta thalassemia — and continues to advance clinical and research programs in these diseases.
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Understanding of the healthcare domain and clinical, epidemiologic, and genomic data is a plus. Our research team oversees study data related activities and quality improvement activities to improve the way translational research is conducted and clinical care is delivered.
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For hospital, routes to billing charge entry errors and/or account edits preventing completion of coding and/or billing. Reviews and validates the accuracy of data in the Admission, Discharge Transfer (ADT) fields following HIM coding procedures and processes.
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Demonstrated proficient knowledge in music therapy clinical practice, musical skills, child development and the impact of healthcare on neurodevelopmental outcomes. This Music Therapist, Oncology will:Provide music therapy to support the developmental, rehabilitative, psychological, socioemotional, and psychoeducational needs of BCH patients and families from various demographic and multicultural backgrounds.
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PCI is proud to serve pharmaceutical, biotechnology, medical device, and clinical research industries nationwide by providing calibration, commissioning and consulting solutions. PCI is an FCX Performance Company and a Subsidiary of Applied Industrial Technologies (NYSE: AIT); a leading industrial distributor that offers more than 6.5 million parts to serve the needs of MRO and OEM customers in virtually every industry.
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The Registered Nurse in the OR is directly responsible to the Clinical manager but may be supervised by the Resource Nurse. Reviews with Pre-op RN the preoperative checklist ensuring all requirements are met before escorting patients to OR.Coordinates care of the patient with the surgeon, anesthesiologist and other personnel as required.
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This client is a growing international full-service CDMO/CRO within the biotechnology space looking to aggressively expand its footprint in the US. The company has a strong base of API/Small Molecule, Biologics, Clinical Research, Bioanalytical Sciences, DMPK, Cell and Gene Therapy and other capability centers across the US. This business has developed a fantastic brand in the US through exceptional service which drives repeat business.
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Analyze LIS data to confirm customer volumes, test menus and validation of project implementation and cost savings results. Collect and analyze before and after data points to ensure cost savings goals are met and customer sign-off in a timely manner.
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Habitat for Humanity: Builds affordable housing to empower families and strengthen communities through volunteer-driven construction projects.
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The position involves collaboration with protein science, in-vivo biology, single-cell sequencing, bioinformatics, translational and clinical teams to execute and advance HiFiBiO’s drug discovery and translational research.
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Communicate opening balances with AVP, Controller and Assistant Controller – highlighting significant transactions to ensure timely posting to general ledger or following up on unusual activity to identify transactions needing a journal entry.
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Data generated by epidemiological studies is critical evidence needed to support clinical development (planning for Phase 3 efficacy trial, including a series of studies to determine incidence and risk groups to inform Phase 3 methodology and identify trial sites), to obtain optimum Vaccine Technical Committee recommendations, schedules, and public payer option, and to develop studies for post-licensure vaccine effectiveness which are pivotal to fulfil Pfizer’s regulatory commitments.
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Oversight and/or development of sample testing plan and delivery of high-quality biomarker data packages to inform clinical development and regulatory strategy. Deep knowledge of immuno-oncology biology, biomarker strategies and application to clinical trials.
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The selected candidate will be tasked with drafting, reviewing and finalizing CMC content and modules for INDs and CTAs, and later, should our clinical trials be successful will also help prepare NDA and MAA related content for the FDA, EMA and other regulatory bodies as needed.
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clinical entry jobs Title: data in Boston, MA
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