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Document Preparation: Draft, review, and file legal documents related to trust and estate matters, such as wills, trusts, powers of attorney, advance directives, and probate petitions. Court Filings: Prepare and file documents with probate courts and other relevant agencies, ensuring compliance with court rules and deadlines.
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Set-up, organize, and maintain clinical study documentation (e.g. Trial Master File documents, clinical study site documents, email correspondence, training materials, etc.) Pharming is seeking to hire a Clinical Trial Assistant (CTA) to bring general administrative support to the Clinical Operations Department and assistance to Project Manager(s), Clinical Project Coordinator(s) and Department Manager/Director(s) on the various tasks associated with conducting clinical trials.
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Manager, Production Master Scheduler #REC Cranford, NJ. You will own the production related ERP Master Data, taking into account batch sizes, work centers, sequences, and other production related inputs.
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The Candidate: Bachelor of Science in Analytical Chemistry/Pharmaceutics with equivalent industry experience Master of Science in Analytical Chemistry/Pharmaceutics preferred or more years of applicable industry experience in support of pharmaceutical product development Expertise in Instrumentation techniques: HPLC, GC, FTIR, UV, KF, and other wet chemistry testing.
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Resolves problems causing payer denial or failed Medicare edits as they involve the charge master. Educates HMH departments and physicians with respect to the use and maintenance of the charge master and charging philosophy.
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Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
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Develop and file, in tandem with the General Counsel and the Compliance Office, mandatory insurance regulatory filings related to ERM, including but not limited to the Enterprise Risk Report and the Own Risk and Solvency Assessment (ORSA) Summary Report.
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Prepare and file immigrant petitions and applications including PERM, I-130, PERM based I-140 petitions, National Interest Waive (NIW), EB1A, B & C -based petitions and I-485 applications to adjust status.
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Our College of Nursing offers a Bachelor of Science in Nursing (BSN) degree program at 23 locations and online post-licensure degree programs and certificates including RN to BSN, RN to MSN, a Master of Science in Nursing (MSN) with six Specialty Tracks, and a Doctor of Nursing Practice (DNP.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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This position is a member of the Cell Therapy Development and Operations (CTDO) organization, which supplies autologous and allogeneic cell therapies for first-in-human and pivotal clinical trials.
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Preferred certifications are Project Management Institute’s (PMI) Project Management Professional (PMP) certification, Lean, Six Sigma, ITIL, COBIT, Certified Scrum Master (CSM), Certified Scrum Product Owner (CSPO), Certified SAFe Scrum Master (SSM), Advanced Project Manager Certification (APMC.
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Certifications/Licenses Required Knowledge, Skills, and Abilities Equipment Utilized Physical Demands and Work Environment Overview The Master of Business & Science degree (MBS) is a degree combining the science curriculum from a traditional science master’s degree with a specialized set of business+ courses – including business, policy, and law.
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Responsibilities and Requirements: Organize clinical trial data (e.g., integrate EDC datasets to analyze data, generate descriptive summaries, etc.) This role will require someone who is creative & resourceful in researching and "grabbing " R packages from the open-sources and at least 3-5 years of clinical trial development experience.
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While performing the duties of this job, the employee is regularly required to stand, walk and use hands and arms to operate general office equipment (PC, telephone, file cabinets, copier, fax machine and printer.
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trials trial master file jobs Title: trial master in Edison, NJ
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