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Licensed Clinical Social Worker LCSWWhat We Offer: No Admin Tasks! Job Requirements: Willingness to travel up to 45 minutes Full Vaccination and Booster Status may be required in some facilities Ability to communicate effectively in English, both verbally and in writing License Requirements: Possession of any of the following licenses in the state in which you've applied is required Licensed Clinical Social Worker LCSWSCT welcomes individuals with a variety of licensure types to join our exceptional team.
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Innova Solutions has a client that is immediately hiring for a Clinical Trials Disclosure Specialist Position type: Full-time Contract Duration: 12 months Location: Giralda Farms (or) Lawrenceville, NJ As a Clinical Trials Disclosure Specialist, you will: The Clinical Trial Disclosure Senior Specialist will provide the operational support of: Redaction of clinical trial documents in accordance with evolving global regulations.
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Represent clients in court proceedings, including hearings, trials, arbitrations, and appeals. Innovative Driven is currently seeking a Commercial Litigation Associate Attorney to join a dynamic and busy law practice in a New Jersey law firm.
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Experience in supporting post-approval studies/ clinical trials, including observational studies, PMR/PASS/PAES type of studies, disease/treatment registry type of studies, investigator-initiated studies/trials, and assessments of electronic health records like claims databases and preparation of health technology assessment (HTA) dossiers.
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Provides oversight of all statistical programming activities performed by contractors in different oncology trials as well as submission-related activities, e.g., integrated summary of safety (ISS) and integrated summary of efficacy (ISE.
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Lead statistical programming activities for multiple clinical trials within a program or an indication/disease area, or development program. In-depth understanding of clinical trials methodology, regulatory requirements, and Good Clinical Practice (GCP.
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Participation in clinical trials can be a very rewarding experience. Participation in clinical trials can be a very rewarding experience. Not only do you get free access to cutting-edge medical treatment, but you are also contributing to science all whilst getting paid.
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If you are physically/mentally ill or healthy, get paid to trial new treatments and medications. Compensation can be up to several thousand dollars depending on the trial. Children with Autism. No experience or education required.
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Identify and assist, as needed, in initiation and closure of investigator-sponsored clinical trials (ISS). Proactively identify potential research sites and assist as needed in facilitation of company sponsored clinical trials.
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Interact with Medical Directors, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.
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Fresh PhD or MS with 2+ years' experience in statistics or biostatistics or related scientific field with clinical trials and/or RWE in pharmaceutical industry or healthcare experience. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
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The position is responsible for implementation and management of system to manage quality throughout all stages of clinical trials and will report to the Vice President of Clinical Operations within the Chief Medical Officer (CMO) organization.
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Join Owen Health Care as a Part-Time/Full-Time Respite Worker and make a meaningful impact from the comfort of your home in Union County! As a Part-Time/Full-Time Respite Worker at Owen Health Care Inc. , you will play a vital role in enhancing the quality of life for families with children who have disabilities.
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This position is responsible for managing Interactive Response Technology (IRT)-related activities across multiple clinical trials and / or at the vendor level according to Good Clinical and Manufacturing Practices (GCP. GMP), and Daiichi Sankyo standard practices.
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Support assessment on opportunity to capitalize on non-traditional options (e.g., historical data, synthetic data, cross-sponsor shared control arms IMI EU-PEARL, adaptive designs, pragmatic trials, decentralization, etc.
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trials job Title: worker Company: Cincinnati Hospital Medical Center in Madison, NJ
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