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Proven track record of leading biomarker programs from conception through validation and implementation in clinical trials. As a Senior Scientist in Clinical Biomarkers, you will be a key player in their research efforts to develop therapies that combat neuromuscular disease.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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May be responsible for scheduling numerous complex research protocols, involving extensive interaction with those associated with in-house studies, grant-funded studies and industry-sponsored clinical trials.
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As the fastest growing behavioral health practice group in the country, now is the perfect time to join our clinical team! We perform essential, yet non-billable clinical and administrative functions that comprise the infrastructure needed to maintain a successful, busy practice so that you can focus on your clinical work.
$100,000 - $135,000 a yearExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Executes foundational quality systems activities (e.g., change control, deviations and investigations, incident notification and escalation, CAPA, etc) for Clinical Research, Pharmacovigilance and Medical are effective and appropriately resourced and supported.
$205,100 a yearExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Collaborate closely with cross-functional teams, including clinical development, non-clinical development, DMPK, regulatory affairs, and clinical operations, to ensure alignment and integration of clinical pharmacology principles throughout the drug development process.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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May include direct line management of Clinical Operations staff. Multi-dimensional Clinical Operations background with capability of devising plans for operational challenges such as site activation, subject enrollment, monitoring oversight, protocol deviation management, data cleaning, etc.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assists Director, Clinical Monitoring in resourcing field CRAs for planned and ongoing clinical trials. We support our clients with a full spectrum of patient-centric data and tech-enabled services including Transaction Advisory, Management Consulting, Real-World Evidence, Advanced Analytics, Patient Engagement, Product Development, Regulatory, Clinical, and Market Access.
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Meet regularly with your Regional Clinical Director. Care is at the center of everything we do at BHW. Our dedicated clinical team works directly with children, adolescents, families, and their network of professionals to achieve meaningful outcomes through evidence-based therapies and techniques.
$89,250 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Design and develop data capturing tools: Electronic Data Capture (EDC) Systems (Eg: iMedidata Rave and IBM Clinical) eCOA, IRT; Manage electronic Trial Master File (eTMF) QC review eg: Veeva Vault; Lead the Audit and Inspection/Submission Readiness activities like documentation of QC and preparing Storyboards (Eg: FDA/EMA Submissions.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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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, eCOA, IRT, CDR, MDR, SCE and adjacent systems.
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The Town of Brookline Council on Aging is seeking applicants for the position of Clinical Social Worker II. The Brookline Council on Aging works with town agencies and the community to provide comprehensive services and enhance the quality of life for Brookline seniors age 60 and over.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Be responsible for protocol design of clinical pharmacology trials, study planning, review, data analysis / interpretation, and reporting of individual studies implemented to support clinical pharmacology components of project plans.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Knowledge of Good Clinical Practices and regulatory requirements for the conduct of high-quality oncology clinical trials is required. This person will work closely with the clinical project scientist team and Clinical Leader in Late Development, in collaboration with other functional disciplines, including GCO, Data Management, Statistics, Regulatory, QMMC, and GMS to ensure flawless and integrated execution of study start-up planning, oversight, and reporting of clinical studies in Oncology.
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Previous experience with clinical trials and/or research coordination and personnel management required. The Senior Research Regulatory Coordinator (RC) works under the direction of the CCI Executive Director, Research Operations Director and Principal Investigator(s) to complete the regulatory requirements of clinical research projects.
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The Clinical Finance Office seeks a Dental Financial Coordinator to oversee the workflow of dental clinical finances related to state Medicaid/Medicare programs, including MassHealth and other identified programs administered by Dentaquest and Skygen/Scion.
Full-timeExpandApply NowActive JobUpdated 6 days ago
Title: clinical trials Company: Parexel in Newton, MA
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