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Role Title: Clinical Associate. Ability to multi-task and use multiple systems, including our EMR to provide medical information and patient support/follow up after the clinical visit.
$22.12 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Purpose The Associate Scientific Director provides medical and scientific strategic and operational input into core medical affairs activities such as: health-care professional and provider interactions (HCP’s, Patients and Payers); generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives (medical education, data, guidelines, and value proposition); safeguarding patient safety (risk minimization activities and safety surveillance activities.
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Banner Casa Grande Medical Center is a 141-bed acute-care hospital located midway between Phoenix and Tucson, AZ. The facility boasts the neighborhood convenience of a community hospital while leveraging the clinical expertise of one of the nation’s leading health systems.
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Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results.
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Actively develops leadership of entry level nurse manager(s) while leading clinical improvement initiatives. We are looking for an Associate Director to help lead this amazing team of patient care professionals working in a fast-paced environment.
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Job Title: Regulatory Studio - Associate Director, Precision Medicine & Digital Health. Worked on drug trials that use a biomarker to select patients into the trial, include but not limited to, understand clinical trial assay (CTA) requirements with diagnostic partners, sample testing/shipping regulations in different countries, and CDx development requirements.
$55 an hourExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol amendments in compliance with HA deadlines. Experience with clinical trial assays (CTA) in drug clinical trials in communicating between Diagnostic sponsor and Drug sponsor.
ExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Job Title: Associate Director, Clinical Safety MD Job Schedule: Candidate can work % remote for duration of assignment. - years of Pharmacovigilance (PV)/clinical safety experience in pharmaceutical drugs either from relevant work experience within the industry or related healthcare work.
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For Associate Director level with Ph. D. approximately 5+ years experience with demonstrated progression clinical pharmacology and Pharmacometrics experience. The Clinical Pharmacology and Pharmacometrics (CP&P) team at BMS is responsible for the pharmacology and pharmacometric support for all pipeline assets throughout the clinical development lifecycle.
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The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs.
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Lead statistical programming activities for multiple clinical trials within a program or an indication /disease area, or development program. The Statistical Programming community at Novartis comprises of approximately 350 (internal) statistical programmers and belongs to the Advanced Quantitative Sciences (AQS) organization which also includes more than 450 biostatisticians, pharmacometricians and data scientists supporting the entire portfolio of clinical projects across the Research, Development and Commercial spectrum.
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Job Title: Associate Director - Clinical Safety ScientistJob Schedule: Candidate must be local and able to go into office 1-2 days a week. Collaborates with PSL/Clinical Safety Physician(s) and cross-functional team to develop safety strategy, key safety messages, and review and author safety sections of Common Technical Document (CTD.
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Position is onsite at the client a minimum 2-3 days every two weeksIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
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Communicate changes in patient's clinical condition with Physicians, Nursing Supervisor/Manager, and co-workers as appropriate. Qualifications Graduated from an accredited Bachelors of Science in Nursing as Registered Nurse / RN or Associate Degree in Nursing or Nursing Diploma program as a Registered Nurse / RN. Current state licensure as Registered Nurse / RN. BCLS certification is required.
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Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines.
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clinical associate jobs in Morris Plains, NJ
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