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📑 JOB DETAILS 1. Ensure thatclinical researchstudies are conducted in accordance with the protocol, standard operating procedures, goodclinicalpractice (GCP) guidelines, and other applicable regulatory requirements. 2. Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guideli ...

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📑 Avance Clinical is a Contract Research Organisation which offers specialised services supporting clinical drug development for the pharmaceutical and biotechnology industry.The Statistical Programming Team Manager is responsible for the oversight of statistical programming operations (including SAS programming and CDISC programming) and team, and f ...

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📑 We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years o ...

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📑 Role Title: Senior/ Principal BiostatisticianLocation: BangaloreNumber of open positions: 2Who are we?We’re Avance Clinical a Contract Research Organization. We offer specialized services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots da ...

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📑 Role Title: Senior/ Principal BiostatisticianLocation: Bangalore Number of open positions: 2 Who are we?We’re Avance Clinical a Contract Research Organization. We offer specialized services supporting drug development for the pharmaceutical and biotechnology industry. We have a rich history in this area with our founding roots dating back to the 19 ...

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📑 We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellenc ...

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📑 Avance Clinical is a Contract Research Organisation which offers specialised services supporting clinical drug development for the pharmaceutical and biotechnology industry.The Statistical Programming Team Manager is responsible for the oversight of statistical programming operations (including SAS programming and CDISC programming) and tea ...

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📑 We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years o ...

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📑 We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years o ...

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📑 We are expanding! We have many new ground-breaking global clinical trial projects in various phases and therapeutic areas across the globe and want your ideas and expertise to help us build and grow.Who are we?A leading global clinical research organization founded in Asia-Pacific driven by scientific expertise and operational excellence20+ years o ...

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📑 Avance Clinical is a Contract Research Organisation which offers specialised services supporting clinical drug development for the pharmaceutical and biotechnology industry.The Statistical Programming Team Manager is responsible for the oversight of statistical programming operations (including SAS programming and CDISC programming) and team, and f ...

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📑 Clinical Research CoordinatorAbout the jobRole DescriptionThis is a full-time hybrid role for a Clinical Research Coordinator with Client. The Clinical Research Coordinator will be responsible for day-to-day tasks related to clinical research, including informed consent, protocols, research, clinical research experience, and clinical trials. This r ...

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📑 JOB DETAILS 1)Research potential vendors 2)Compare and evaluate offers from suppliers 3)Negotiate contract terms of agreement and pricing 4)Track orders and ensure timely delivery 5)Review quality of purchased products 6)Enter order details (e.g. vendors, quantities, prices) into internal databases 7)Maintain updated records of purchased prod ...

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📑 Position Title : Executive / Assistant Manager - Clinical Operations (Clinical Research Associate)Location : Bangalore At VIATRIS™, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthie ...

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📑 Position Title : Executive / Assistant Manager - Clinical Operations (Clinical Research Associate)Location : Bangalore At VIATRIS™, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthie ...

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📑 Position Title : Executive / Assistant Manager - Clinical Operations (Clinical Research Associate)Location : BangaloreAt VIATRIS™, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwi ...

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📑 Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative ...

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📑 Job Title: Clinical Research Associate (CRA)Company: MS Clinical Research Pvt LtdAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the development of innovative ...

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📑 Job Description 1. Preparation of SOPs for Clinical Quality and Safety 2. Analysis of clinical quality indicators across Practo FFH and preparation of dashboard for review. 3. Periodically perform medical records audits, clinical processes for compliance. 4. Compilation of Clinical incident reports (Medical Code Red events), maintaining a ...

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📑 Job Title : Clinical Research Associate (CRA)Company : MS Clinical Research Pvt LtdAbout Us :MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to conducting high-quality clinical trials and contributing to the de ...

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📑 When our values align, there's no limit to what we can achieve. Clinical Trial Protocol Specialist The Clinical Trial Protocol Specialist will research, create, and edit clinical trial protocols as well as provide expert support for protocol development. Operates as a lead medical writer or as a Subject Matter Expert (SME) to support Medica ...

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📑 Department: EU Submissions Hub Are you ready to make a difference in the lives of millions of people living with a serious chronic disease? Join Novo Nordisk, a proud life-science company on a mission to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Tri ...

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📑 Senior/Lead Statistical Programmer Full-Time Bengaluru, Karnataka, India Hyderabad, Telangana, India Description Job Responsibilities: • Annotate Case Report Form ( following FDA/CDISC or sponsor guidelines. • Develop SDTM specifications and generate SDTM datasets using SAS. • Develop ADaM specifications and generate ADaM datas ...

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📑 JOB DESCRIPTION:Experience Level: 5+ years onlyBrief description of the jobAs a Clinical Statistician, you provide expert statistical input and contribute to development plans, design, protocol writing, statistical analysis and interpretation of results from clinical studies. You are accountable for timely availability of high-quality analysis resu ...

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📑 JOB DESCRIPTION:Experience Level: 5+ years onlyBrief description of the jobAs a Clinical Statistician, you provide expert statistical input and contribute to development plans, design, protocol writing, statistical analysis and interpretation of results from clinical studies. You are accountable for timely availability of high-quality analysis resu ...

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📑 Job Duties & Responsibilities Act as a Service Owner, ultimately responsible for the success of assigned services. This may include but is not limited to driving service development and expansion, providing updates to leadership, and acting as the primary liaison and expert for the service across the company. Work closely with the Business ...

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📑 Company Overview:iProcess is a leader in biospecimen collection studies, providing key contributions to the advancement of medical research. Our speciality in the procurement and handling of quality biospecimens underpins crucial developments in medical diagnostics and therapies. For more information about our dedicated approach to medical research ...

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📑 The position As Regulatory Professional, you will play a crucial role in driving, coordinating, and actively following up on multiple tasks with challenging timelines. Your responsibilities will include: Working closely with various submission teams across the organization and all countries in Europe Managing initial clinical trial applicatio ...

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📑 Visualisation - CT, MRI (C++, VTK, OpenCV, Medical Image Processing) Must Have - - C++ (QT, Boost, Design Patterns) - Data Analytics, Algorithms, Image Processing, Visualization Desirable - - Proven research record and high quality publications in image processing, visualization or related areas. - Experience with one or more of the fo ...

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📑 Department: Data Management Operations and Insights Are you passionate about analyzing data and providing valuable insights? Are you ready to join a dynamic team and make a difference in the healthcare industry? We are looking for a skilled Lead Clinical Programmer to join our Data Management Operations and Insights department at Novo Nordisk. ...

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📑 When our values align, there's no limit to what we can achieve. Job Purpose: The Clinical Operations Leader is responsible for coordinating the functional team members and their activities across all geographies, liaising with project leadership and the sponsor to ensure that the Clinical Operations deliverables (timeline, quality, productivi ...

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📑 Company Overview:iProcess is a leader in biospecimen collection studies, providing key contributions to the advancement of medical research. Our speciality in the procurement and handling of quality biospecimens underpins crucial developments in medical diagnostics and therapies. For more information about our dedicated approach to medical rese ...

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📑 JOB TITLE : Associate Director- Clinical Regulatory Writing CAREER LEVEL: E Lead the way for a new breed of solutions-oriented Regulators Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious enterprise-thinkers we proactively take a strategic approach earlier in the product lifecy ...

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📑 JOB TITLE : Associate Director- Clinical Regulatory Writing CAREER LEVEL: E Lead the way for a new breed of solutions-oriented Regulators Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious enterprise-thinkers we proactively take a strategic approach earlier in the product lifecy ...

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📑 Data Facilitation Programmer Department: Data Systems & Automation (DSA) Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an ...

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📑 DescriptionIntegrated Data Analytics and Reporting (IDAR)Position Title*: Statistical Programming LeadPosition Summary The Statistical Programming Lead is an experienced Statistical Programmer with advanced knowledge of statistical programming methods, languages and data structures and capabilities in leading analysis and reporting a ...

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📑 Essential FunctionsApply machine learning and AI techniques to analyze data and generate predictive insights.Develop and integrate advanced analytics models within Azure Synapse and Power BI dashboards.Collaborate with Business Analysts to translate business needs into data science projects.All other duties and responsibilities as assigned.Skills n ...

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📑 Primary Duties and Responsibilities Project Management Responsibilities: Act as a back-up for the designated tasks in the absence of the manager. Work as a liaison between manager and the team. Collaborate with manager to Identify the future tasks for Operations team and develop the plan. Maintain high level quality for all the tasks. ...

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📑 Primary Duties and Responsibilities Project Management Responsibilities: Act as a back-up for the designated tasks in the absence of the manager. Work as a liaison between manager and the team. Collaborate with manager to Identify the future tasks for Operations team and develop the plan. Maintain high level quality for all the tasks. ...

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📑 JOB TITLE : Associate Director- Clinical Regulatory Writing CAREER LEVEL: E Lead the way for a new breed of solutions-oriented Regulators Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious enterprise-thinkers we proactively tak ...

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📑 JOB TITLE : Associate Director- Clinical Regulatory Writing CAREER LEVEL: E Lead the way for a new breed of solutions-oriented Regulators Champion a new approach to Regulatory that supports quick decision-making and balanced risk-taking. Curious enterprise-thinkers we proactively tak ...

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📑 • Lead the conduct of analytics within the TriNetX platform in support of epidemiological investigations, clinical trial protocol feasibility, and planning for clinical trial implementation. • Ensure the training of users of the TriNetX platform for clinical trial planning. Work with Epidemiology leadership to quantify the use of the TriNetX platfo ...

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📑 Statistical Programmer - CREQ185924 Description JD: Bachelor's or Master's degree in statistics, biostatistics, computer science, or a related field. Minimum of 7-10 years of experience in statistical programming in the pharmaceutical, biotechnology, or clinical research industry. Implements statistical programming aspects of the protocol or clinic ...

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📑 Department: Data Systems & Automation (DSA) Are you passionate about what you are doing? Do you want to build excellence within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment? Are you best at what you do? If so, raise your hand as there is an exciting opportunity waiting for ...

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📑 Department: Data Management Operations and Insights Are you passionate about analyzing data and providing valuable insights? Are you ready to join a dynamic team and make a difference in the healthcare industry? We are looking for a skilled Lead Clinical Programmer to join our Data Management Operations and Insights department at Novo Nordisk. ...

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📑 Department : Global Safety. Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career objectives? Then we might have ...

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📑 Essential Functions Apply machine learning and AI techniques to analyze data and generate predictive insights. Develop and integrate advanced analytics models within Azure Synapse and Power BI dashboards. Collaborate with Business Analysts to translate business needs into data science projects. All other duties and responsibilities as a ...

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📑 Job Title: Business Development - GenomicsCompany: MS Clinical Research Pvt Ltd-BangaloreLocation: BangaloreAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to leveraging cutting-edge technologies and innovative methodolog ...

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📑 Job Title: Business Development - GenomicsCompany: MS Clinical Research Pvt Ltd-BangaloreLocation: BangaloreAbout Us:MS Clinical Research (MSCR) is a leading clinical research organization dedicated to advancing scientific discovery and improving healthcare outcomes. We are committed to leveraging cutting-edge technologies and innovative methodolog ...

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📑 Department: Study Data Tabulation Model Programming & Submission Does your motivation come from challenges and working in a dynamic environment? Do you thrive in a working environment where close collaboration with key stakeholders and strategic alignment is essential? Do you have a can-do attitude with continuous improvement as one of your career ...

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