- Genmab (NJ)
- …a fit? Then we would love to have you join us!The Global Regulatory Labeling, Policy and Intelligence Associate Director will primarily be responsible for leading ... portfolio of products. The lead may also be responsible for supporting various regulatory policy and/or intelligence deliverables. This role will be within Global … more
- Genmab (NJ)
- …us!The RoleThe Associate Director acts as a statistical expert supporting the clinical development of compounds as compound and/or indication lead for both early ... responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication LevelAct as lead and… more
- Genmab (NJ)
- …Medical Writing Manager to help us tell the story of our science through compelling clinical and regulatory documents. You'll be at the heart of a team that ... Global Medical Writing team, you will drive the development of high-quality clinical documents to support operational, medical, and regulatory activities across… more
- Genmab (NJ)
- …us!The Role:The Senior Statistical Manager acts as a biostatistician supporting the clinical development of compounds as compound lead, primarily up until proof of ... methodologies that may support innovation and improve efficienciesEngage with regulatory authorities on compound/indication level discussionsActs as a role… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Role OverviewThis position will be responsible for metrology support for cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with ... to cGMP requirements. This individual will support organization build and ramp-up of clinical production and facility approval of a state of the art cell therapy… more
- Legend Biotech USA, Inc. (Baton Rouge, LA)
- …team. Direct education for healthcare professionals treating oncology patients on clinical data, adverse event management, and mechanism of action for commercial ... Affairs strategies and tactics.Assist in the oversight of Legend Biotech sponsored clinical trial sites to include, but not limited to, site identification, patient… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …be responsible for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift ... requirements. This individual will support the organization in its build and ramp-up of clinical production and facility approval of a state of the art cell therapy… more
- Eisai, Inc (Salt Lake City, UT)
- …will have the primary role of demand generation by conveying complex clinical information to customers and key stakeholders consistent with the FDA-approved ... demand generation within assigned geography by effectively conveying complex clinical information to customers and key stakeholders.Develop, maintain, and execute… more
- Eisai, Inc (Nutley, NJ)
- …opportunities for evolution and differentiation.Collaborate with our Global Marketing, Clinical Development, and Government Affairs on the go-to-market strategy for ... project teams involving Marketing, Sales, Managed Markets/Market Access, Legal, Regulatory , Medical, PR, agencies, actively soliciting team expertise and input… more
- Genmab (NJ)
- …Manager will support the Data Management, Statistics, Drug Safety, Medical, Clinical Pharmacology and Biomarker functions with the above by developing and ... checks of data consistenciesSupports specification and pooling of data across clinical trials within the same project.Supports in-house production of analysis… more
- Eisai, Inc (Phoenix, AZ)
- …customer business, disease state, product prescribing information, approved promotional clinical trials, patient access to medication, and regulatory /compliance ... decision-makers through understanding of issues and opportunities in territory. Deliver clinical , efficacy, and safety messaging and information about product access… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …systems, and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment. This role will ... aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy.Knowledge of cGMP regulations and FDA/EU… more
- Mount Sinai Hospital (New York, NY)
- …resources. 5. Documents in an accurate and thorough manner in compliance with hospital , regulatory and legal requirements and standards of care. 6. Facilitates ... Job Description The Clinical Nurse is a Registered Professional Nurse who...patient care including teaching, rounding, coaching, and planning after hospital care and delegating to others as appropriate. 6.… more
- Mount Sinai Hospital (New York, NY)
- Job Description Job Title: Clinical Nurse-MedSurge-Stepdown-10W-Mount Sinai Hospital -PT/Days The Clinical Nurse is a Registered Professional Nurse who ... other resources. Documents in an accurate and thorough manner in compliance with hospital , regulatory and legal requirements and standards of care. Facilitates… more
- MLee Healthcare Staffing and Recruiting, Inc (Trabuco Canyon, CA)
- …laboratory personnel as necessary. Maintain all laboratory records in compliance with hospital policies and regulatory requirements. Clinical Laboratory ... Clinical Laboratory Scientist-CLS Hospital Based Position Competitive salary, comprehensive benefits, and career development opportunities. Sign-On Bonus… more
- Mount Sinai Hospital (New York, NY)
- Job Description The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies ... under the supervision of the Principal Investigator or senior clinical research staff. This individual obtains informed consent, collects, maintains and organizes… more
- Children's National Hospital (Washington, DC)
- …day-to-day research program operations following Standard Operating Procedures (SOPs), Good Clinical Practices (GCP) and regulatory guidelines, company goals, ... The Clinical Research Program Manager will serve as a...issues, develops systems to track multiple projects including all regulatory files, investigator and IRB information, patient recruitment activity… more
- Mount Sinai Hospital (New York, NY)
- …the resolution of potential safety hazards and validation of compliance with hospital and departmental policies and procedures and regulatory agency standards. ... Directors to ensure communication about progress, changes and compliance with all hospital policies and procedures and regulatory agency standards. 12.… more
- Mount Sinai Hospital (New York, NY)
- …team members on patient recruitment, data collection, participant tracking, maintaining regulatory documents, and medical chart abstraction. You will be one of ... and detail-oriented. The study involves quite a lot of regulatory paperwork, and an eye for detail and skill...study data from medical records. Work cooperatively with other clinical and research staff members. Be flexible; schedule may… more
- Monadnock Community Hospital (Peterborough, NH)
- …compassionate and respectful care. Adherence to Policies and Regulations: Comply with hospital policies, procedures, and regulatory guidelines to maintain a safe ... The position of the Clinical Coordinator was developed to facilitate the functioning...the guidelines of accepted nursing practice, medical direction, and hospital policies, procedures, and standards. The RN utilizes the… more
