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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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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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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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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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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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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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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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One of our largest CPG clients in Florham Park, NJ is looking for a team of Senior Associate Analytical Scientists to join their analytical department for a long-term remediation project. They will be responsible for supporting analytical method development, validation, method transfer, clinical sample testing, validation sample testing, and characterization of developmental formulas for sun care and other derma topical formulations.
$53 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Common Job Titles: We frequently fill positions such as Research Scientist, Clinical Research Associate, Quality Assurance Specialist, Regulatory Affairs Manager, Pharmaceutical Sales Representative, and more.
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The Associate Director will be primarily responsible for the business, operational, and compliance aspects of Oncology drug discovery, development, and marketed products at Gilead. Works collaboratively with Statistical Programmers, Biostatisticians, Clinical Research, Clinical Data Managers and other Clinical, Global Drug Safety, Regulatory and Project Management colleagues to meet project deliverables and timelines for statistical data analysis and reporting.
$225,060 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Minimum 6 years of experience working in the CRO matrix environment managing global development program as a Lead Clinical Research Associate (CRA)/Clinical Trial Lead (CTL) or Clinical Program Lead (CPL) preferred.
$84 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The R&D Sourcing and Contracting Associate will be responsible for assistance in the pre-clinical / research, clinical sourcing in support of Gilead’s global Phase I-IV clinical trials, and other ad hoc projects in the Vendor Outsourcing department.
$67 an hourExpandApply NowActive JobUpdated 16 days ago - UpvoteDownvoteShare Job
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Associate Degree required; Bachelor’s degree preferred. Atlantic Health System is seeking a Per Diem Respiratory Therapists for the Morris Plains Clinical Services Unit. The position will be working approximately 2-day shifts per week - 8:30 - 5pm Monday -Friday.
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Develop and implement or update policies, SOPs, guidelines, and associated internal communications related to non-promotional, medical/clinical programs, including congress activity, educational programs, use of publications and reprints, commercial medical interactions, advisory boards, ad hoc consulting, IITs, clinical trials, Mock FDA meetings, etc.
$254,150 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Clinical Trial Associate (CTA), Clinical Operations - Contractor will support the clinical project team in the operational execution of clinical trials. Must possess basic knowledge of applicable clinical research regulatory requirements including, Good Clinical Practices (GCP.
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clinical associate jobs in Dover, NJ
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