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Design Project Manager Salary in Florham Park, NJ

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Agile Project Manager

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Applications Manager

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Applications Project Manager

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Architect Project Manager

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Assistant Project Manager

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Associate Project Manager

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Business Project Manager

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Capital Project Manager

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Clinical Project Manager

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Customer Project Manager

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Digital Project Manager

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Electrical Project Manager

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Facilities Project Manager

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Finance Project Manager

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General Project Manager

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Global Project Manager

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Healthcare Project Manager

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Implementation Project Manager

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Infrastructure Project Manager

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International Project Manager

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Marketing Project Manager

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Principal Project Manager

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Program Coordinator

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Project Assistant

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Project Control Manager

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Project Controls Manager

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Project Coordinator

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Project Integrator

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Project Management Consultant

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Project Manager

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Project Officer

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Project Specialist

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Security Project Manager

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Software Project Manager

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Support Project Manager

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Systems Project Manager

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Technical Project Manager

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Technology Project Manager

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Testing Project Manager

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Training Project Manager

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Utilities Project Manager

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Senior Trial Manager, Clinical Operations
Shionogi Inc., Florham Park
The Senior Trial Manager, Clinical Operations is responsible for conduct of global clinical studies.  With minimal oversight, manages CRO and vendor performance to ensure that clinical studies are completed in accordance with contract specifications and management’s expectations. RESPONSIBILITIES  Oversee and manage all operational aspects of phase I – IV global clinical trials in order to achieve a high quality product for the marketplace and business success for Shionogi Inc. Manage external partners, consultants, vendors and budget to ensure the timely and cost-effective implementation of clinical trials. Coordinate the assessment of CROs and preferred vendors for implementation of clinical development plan. Review contracts, work orders and invoices prior to submission to senior management for approval. Establish and maintain effective communication and collaboration with functional area peers including Pharmacovigilance, Drug Supply, Quality Assurance, Regulatory Affairs, Legal, Medical Writing, Biostatistics and Data Management to meet program objectives and support achievement of goals. Responsible for resource requirements (time, financial, manpower) within Clinical Research and management within agreed upon parameters. Responsible for completeness and accuracy of the study synopsis, protocol, case report and informed consent forms, clinical study reports, Annual Reports, and IB. Responsible for leading protocol and study specific clinical and operational meetings. Contribute to and support selection of all study-related vendors. Specific Duties Accountable for working closely with Shionogi Biometrics, Data Management, Pharmacovigilance and the CRO (when appropriate) to complete data management and bio-statistical analysis and oversee adherence to study timelines and data quality. Oversight includes the following areas: query resolution, logic edit checks, data line listing review, QA/QC of adverse events, and serious adverse event processing. Responsible for managing relationships with CROs and other vendors for all study activities including study start-up, close out, and completion of Trial Master File. Responsible for initial RFP obtainment and contributes to CRO/vendor selection Responsible for setting up, negotiating, and monitoring Task Order invoice payments for CRO (direct service and pass through costs); as well as oversee scope change negotiations. Responsible for negotiating site CTAs in conjunction with the Legal Department and CRO. Responsible for patient recruitment and retention plans Responsible for the set-up of all third party vendor specifications (ie. IWRS, eCRF, central laboratory/ECG, etc.) and on-time third party deliverables. Responsible for collecting, preparing and reviewing regulatory documentation for IRB submission prior to study start-up. Responsible for participating and presenting at Investigator Meetings. Responsible for program level budget forecasting and quarterly review. In conjunction with Drug Supply, responsible for assuring sufficient clinical drug supply is packaged, available and shipped to sites for study start up, and that sufficient supply are maintained during the study. Responsible for assuring accurate drug accountability/reconciliation for IP issued during the study to the site and at the end of the study. In conjunction with CRO responsible for assuring sufficient ancillary supplies are available and shipped for the study (i.e., templates, binders, forms, supplies, etc.). Responsible for preparing and/or presenting executive management slide decks. MINIMUM JOB REQUIREMENTS  BA/BS in life sciences or equivalent; or RN/BSN. Advanced degree or certification preferred At least 6 – 8 years of clinical research experience, with a minimum of 4 years having effectively led a project from inception to completion coupled with demonstrated ability to hold team members accountable with minimal oversight. Demonstrated expertise in daily oversight of CRO relationships and activities and a track record for completing trials on time and within budget. Knowledge of pharmacokinetics and pharmacodynamics with other supportive scientific and/or medical background. Experience and knowledge dealing with Phase 1 studies is an advantage. Significant knowledge of pharmaceutical industry, drug development and regulatory processes in order to maintain compliance with all applicable regulatory guidelines, GCP and Company SOPs and policies. Proficient computer skills and knowledge of standard office software. Ability to travel 10%-15% including possible international travel. PREFERRED SKILLS & EXPERIENCE  Previous experience as a Clinical Research Associate preferred, but not mandatory Strong written and verbal communication skills along with excellent interpersonal skills. Able to make effective presentations across functions and to senior management. Demonstrated ability to resolve multifaceted problems and lead multiple projects of diverse scope, analyze data and exercise sound judgment. High sense of urgency and ability to proactively identify critical path items and develop contingency plans to mitigate risk to budget, quality, and/or timelines. Work comfortably within a fast-paced and dynamic work environment and ability to embrace change. 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Other requirements, duties and responsibilities may change or be assigned at any time with or without notice.  You acknowledge and agree that information described herein may be disclosed to applicable regulatory authorities, alliance partners and/or third party service providers as necessary for Shionogi to fulfil its obligations under applicable laws, including but not limited to compliance with regulatory inspections and/or audits. EEO Shionogi Inc. is an equal opportunity/affirmative action employer. All qualified applicants will receive equal consideration for employment opportunities based on valid job requirements without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity, marital status, national origin, age, ancestry, citizenship, disability, genetic information, status as a disabled veteran, a recently separated veteran, Active Duty Wartime or Campaign Badge Veterans, and Armed Forces Service Medal Veterans, or any other characteristic protected by applicable law. It is the policy of Shionogi Inc. to undertake affirmative action in compliance with all federal, state, and local requirements to recruit a diverse pool of applicants and to ensure that our employment practices are, in fact, non-discriminatory.  Equal Opportunity Employer/Protected Veterans/Individuals with DisabilitiesThe contractor will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information. 41 CFR 60-1.35(c) Clinical Development
Design Apprentice
Incedo Inc., Florham Park
The CompanyIncedo Inc. is a New Jersey headquartered, data, analytics, design and technology solutions firm with offices all around the globe. We work across Wealth Management, Banking, Life Science, and Hi-Tech sectors. We are a global digital transformation expert empowering companies to realize sustainable business impact from their digital investments. We focus on select emerging technologies and build domain-specific solutions which will make the biggest difference to our clients' business.Description:As a Design Trainee, you'll work with a cross-functional, highly capable team of UX Designers, researchers, product managers, and engineers, inventing and iterating end-to-end product experiences. We are looking for designers who are passionate yet capable to analyze customer behaviors and identify opportunities while being able to articulate human-centered approaches in a fast-paced environment. We're a young and passionate team committed to creating a convenient, delightful and intelligent user experience. Job Description:You will be working with our US design team, involved in the end-to-end design process for various products (mobile and web) to serve the global market audience.You will have experience in defining and communicating design guidelines to maintain competitiveness.You will influence and work to bring teams together to drive towards a singular goal of making a product design successful.You will have a chance to collaborate with cross-functional teams to define, design and deliver forward-looking solutions.You will have a chance to experience cross-platform designs (Web/App) and develop your ideas with user research, prototypes, wireframes, storyboards and evaluate your success through usability testing.Collaborate with internal and external stakeholders to test ideas and to quickly iterate on products/featuresWhat you'll getProject experience and a portfolio case study reviewed by our hiring managers to leave with.Domain expertise in either Financial Services, Telecom, or HealthcareExperience working with global teams in India and North AmericaMentorship in a team with a rock-solid Design Process Requirements:Bachelor's/Master's degree in Human-Computer Interaction, UX Design, Interaction Design, or another program with outstanding fundamental design skills and genuine interest to venture into a career in digital design. OR a UX/UI Bootcamp program0-3 years of experience designing mobile sites, web applications, SaaS platforms, or enterprise software (internships count)Good understanding of the design philosophy and practical experience in user experience design and related fields.General understanding of research methodologies.Ability to move, adapt to change, and iterate quickly. Capable of working in collaborative teams to define use cases, and requirements and deliver the best experience for millions of customers.Experience with Figma is a must.Please provide your portfolio in addition to your resume. It can be an attached soft copy or a URL. Profiles without a portfolio included will not be considered.
Building Automation Project Manager
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Database Specialist Senior
Itcsoutions, Florham Park, NJ, US
Database Specialist with Mongo DB.Expertise in Mongo DB Handson,• Performance Tuning on systems built on MongoDB• Experience in large highly scalable and resilient systems using MongoDB.• Looking for real/deep technical expertise in Mongo space.• Looking for prior experience in designing/architecting/building a resilient and highly scalable Mongo infrastructure.• Translates to having played a hands-on role around Mongo clustersWe are a collaborative and fast-growing team working on exciting and innovative digital product offerings.• This role will be for a Senior Database Specialist with prior experience working on NoSQL databases including Mongo. Candidate will serve as a technical architect reviewing all the database design decisions as we look to build next generation Portfolio.• Management platform. This role will have end to end accountability during design, development, unit testing, supporting multiple test phases, deployment and also ownership of the databases after releasing to production.Key Responsibilities• As a Senior Database specifical, you will play a pivotal role in driving and shaping Pershing X Trading and Rebalancing’ data strategy as we start on exciting initiatives to build a highly scalable and incredibly resilient Portfolio Management system in Pershing X space. Working closely withthe team and your peers, will be responsible for• The Design and Delivery of data solutions using Mongo, with an emphasis on quality automation and continuous integration.• Supporting the development and implementation of a data strategy that enables current and future data processing, analytics and reporting requirements in alignment with the overall Pershing X’ data strategy and priorities.• Contributing to the development and implementation of appropriate practices, standards, governance and risk management processes for data deliveryEvaluation of different architectural and software solutions, understanding trade-offs and designing, delivering appropriate solutions. In the business-facing role, you will be working in a fast-paced environment and should be able to share ideas and fresh perspective based on your prior experience(s) Working to collaborate with peers and contribute to new technology discussions.• Building strong relationships with business stakeholders, collaborate on requirements, relationships and ensuring that the technology deliveries are aligned with business goals and strategy.• Writing reusable, testable and efficient code besides coming up with best practices for information security and data protection.Job Specific Competencies Technical Skills/System Knowledge( and associated skill level)• Bachelor's degree in computer science engineering or a related discipline, or equivalent work experience required.• A Minimum of 8 years of experience in software development required; Good understanding of financial markets with prior experience in building, supporting front[1]office trading systems is a plus.• Minimum 5 years of experience around building highly scalable systems using MongoDB.• Demonstrable experience building data pipelines in Python.• Experience building on the Public Cloud (preferably Azure or AWS)• Experience using cloud based PaaS data platforms such as Snowflake and Databricks.• Experience with modern opensource ETL/ELT and orchestration tools such as Airbyte or Airflow.• Experience with data modelling for both operational and analytical datastores• Experience with data lake concepts and strong understanding of data design patterns culminating into microservices development.• Experience in developing Data Pipelines to support near-real-time and event-driven messaging and data processing.• Expertise in Agile development• Experience in handling high volume data processing through concurrency and multi[1]threading techniques to build scalable, performant and resilient applications.• Collaborate cross-functionally with data engineers, business users, project managers and other engineers to achieve elegant solutions.