Healthcare Salary in Karnataka - PayScale

Department :Centralised Monitoring Unit (CMU): BangaloreDoes 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 the right position for you. Apply now and join a growing team, working in an international environment.About the departmentThe Centralised Monitoring Unit (CMU): Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Functional programmers, statistical monitors). Medical reviewers actively involved in Risk based medical monitoring in collaboration with the medical specialists from Denmark, with focus on ensuring overall patient safety and wellbeing of all clinical trial participants, by ensuring compliance to protocol and identifying potential clinically significant outliers that requires medical attention and medical data cleaning. The Functional Programmers develop operational visualisations in data visualization tools to support the trial teams on proactive centralised monitoring and Statistical Monitors perform detection of unusual data patterns, systematic errors and potential lack of compliance or fraud across trials.Job Level: 6The Position:(Note: This is not a role within Pharmacovigilance)The Key Responsibilities in this position will be to perform Medical Review of all trial subjects of all assigned clinical trials within drug development portfolio across therapy areas and to ensure high quality consistent medical data. Medical Review is performed for all trial subjects to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and Standard Operating Procedure (SOPs). Medical Reviewer ensures high quality medical data through medical review of clinical trial data. Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s) and Medical Specialists during trial conduct. Report status of medical review to project as appropriate, following the project communication plan and blinding plan. Consult with Trial Managers and Medical Specialists as appropriate to ensure medical review issues are escalated in a timely manner.:Responsible for contribution to or participation in trial planning activities related to medical review.:Responsible for clarifying and if possible, resolving issues of medical concern and inconsistencies in clinical trial data with staff at investigational sites.:Responsible for presenting findings of Medical Review to relevant Medical Specialist to enable decision making. Responsible for documenting medical review in the sponsor TMF.:Ensure close collaboration with relevant study group members, especially the Data Manager , Trial Manager(s) and Medical Specialist during trial conduct.:Review and provide inputs to MMP as well as Medical Monitoring, Displays or other data listing required to perform Medical review. The input should ensure unambiguous monitoring requirements as well as medical monitoring displays and data listing to enable efficient medical review.Qualifications::Minimum as Graduate in Medicine or other relevant (MBBS and MD in pharmacology preferred, MBBS and MD in other clinical/paraclinical areas with relevant experience in clinical patient management/ clinical research).:2 + years of experience as Medical Reviewer is preferred.:Good knowledge of ICH (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use), GCP (Good clinical Practice).:Demonstrated computer skills (MS Office, MS Project, PowerPoint).:Excellent understanding of medical termin

Department :Centralised Monitoring Unit (CMU): BangaloreDoes 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 the right position for you. Apply now and join a growing team, working in an international environment.About the departmentThe Centralised Monitoring Unit (CMU): Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Functional programmers, statistical monitors). Medical reviewers actively involved in Risk based medical monitoring in collaboration with the medical specialists from Denmark, with focus on ensuring overall patient safety and wellbeing of all clinical trial participants, by ensuring compliance to protocol and identifying potential clinically significant outliers that requires medical attention and medical data cleaning. The Functional Programmers develop operational visualisations in data visualization tools to support the trial teams on proactive centralised monitoring and Statistical Monitors perform detection of unusual data patterns, systematic errors and potential lack of compliance or fraud across trials.The Position: (Note: This is not a role within Pharmacovigilance) The Key Responsibilities in this position will be to perform Medical Review of all trial subjects of all assigned clinical trials within drug development portfolio across therapy areas and to ensure high quality consistent medical data. Medical Review is performed for all trial subjects to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and Standard Operating Procedure (SOPs). Medical Reviewer ensures high quality medical data through medical review of clinical trial data. Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s) and Medical Specialists during trial conduct. Report status of medical review to project as appropriate, following the project communication plan and blinding plan. Consult with Trial Managers and Medical Specialists as appropriate to ensure medical review issues are escalated in a timely manner.:Responsible for contribution to or participation in trial planning activities related to medical review.:Responsible for clarifying and if possible, resolving issues of medical concern and inconsistencies in clinical trial data with staff at investigational sites.:Responsible for presenting findings of Medical Review to relevant Medical Specialist to enable decision making. Responsible for documenting medical review in the sponsor TMF.:Ensure close collaboration with relevant study group members, especially the Data Manager , Trial Manager(s) and Medical Specialist during trial conduct.:Review and provide inputs to MMP as well as Medical Monitoring, Displays or other data listing required to perform Medical review. The input should ensure unambiguous monitoring requirements as well as medical monitoring displays and data listing to enable efficient medical review. Qualifications::Minimum as Graduate in Medicine or other relevant (MBBS and MD in pharmacology preferred, MBBS and MD in other clinical/paraclinical areas with relevant experience in clinical patient management/ clinical research).:2 + years of experience as Medical Reviewer is preferred.:Good knowledge of ICH (International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use), GCP (Good clinical Practice).:Demonstrated computer skills (MS Office, MS Project, PowerPoint).:Excellent understanding of medical

Department : Commercial and Corporate Affairs, GBSAre you experienced in contract management within the healthcare or pharmaceutical industry? Are you adept at engaging and collaborating with different digital technology companies for the purpose of building partnerships by following good contract management procedures? If so, we have an exciting opportunity for you to join our team as a DH Partnership and Contract Manager at Novo Nordisk. Apply today for a life:changing career.About the departmentThe DH Partnership and Contract Manager position is part of the Commercial and Corporate Affairs : Global Business Services (GBS) unit at Novo Nordisk. The Commercial GBS unit is responsible for driving deliverables for multiple Corporate Vice President areas within Commercial Strategy and Corporate Affairs. In the Diabetes Therapeutic Area, we are a passionate team helping millions of people with diabetes achieve better health outcomes through innovative medicines and solutions. We drive and execute projects across a strong portfolio comprising both launch and life:cycle management brands.The positionAs a DH Partnership and Contract Manager at Novo Nordisk, you will be responsible for::Managing the creation, review, and approval of contracts with external partners and creating and managing Service Agreements, SOWs, and project agreements based on best practices and working with affiliates to ensure execution based on global contract.:Monitoring, maintaining, and updating contracts with external partners as necessary and Serving as the singular point of contact for matters concerning contracts in Digital Health Partnerships and Creating and maintaining agreement templates in the contract management system.:Drafting contracts in line with partnership team needs with relevant stakeholder input and managing the review and resolution of comments among internal stakeholders and external partners and working with affiliates to ensure execution based on global contracts.:Investigating and addressing any contract:related issues and Initiating approval and signature of contracts by internal stakeholders and external partners.:Ensuring timely execution of activities and/or payments defined in contracts and Ensuring compliance with all company policies, procedures, and standards, also Identifying opportunities for improvement of contract:related processes and platforms.QualificationsTo be successful in this role, you should have the following qualifications::A bachelor's degree in business or a related field.:6+ years of experience in project management, contract management, legal and compliance, or quality within the healthcare or pharmaceutical industry.:Previous experience working with and/or managing contracts.:A solid understanding of legal terminology.:Familiarity with quality:related processes and best practices.:Technical skills: MS Word, MS PowerPoint, MS Excel.Working at Novo NordiskNovo Nordisk is a leading global healthcare company with a 100:year legacy of driving change to defeat serious chronic diseases. Building on our strong legacy within diabetes, we are growing massively and expanding our commitment, reaching millions around.ContactTo submit your application, please upload your CV online (click on Apply and follow the instructions).Apply Now Deadline3rd April 2024We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve an

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The Product Owner is responsible for the definition and delivery of a part of a product from a customer and market requirement point of view - regarding content, prioritization, quality and customer excitement for a given cost and time frame.• Responsible for a part of the product through the product life cycle from the definition to the phase-out.• Provides the associated development teams with priorities and expertise regarding the product and ensures completeness and consistency of the derived requirements within the part of the product.• Responsible for definition and delivery of a part of a product from a customer and market requirement point of view, working with one or several development teams.Internal Interactions: Product Line Manager, Product Manager, Project Manager, Quality Manager, Development Team (e.g. Scrum Master, System Analyst, Architect, Developers, Testers), Usability Engineer, other stakeholders (e.g. Business Units),Technical Writers.External Interactions: Collaborative customers, Customers, Cardiologists, Sonographers, Hospital Administrators and IT Administrators etc.What are my tasks?• Elicit and collect stakeholder requests• Define and prioritize Market Requirements along with Product Managers.• Analyze Market Requirements (e.g. initiate and manage concepts for complex Market Requirements)• Derive, prioritize and communicate Software Requirements• Create Software Requirement Specifications (i.e. problem part) • Coach/ support development team's questions and resolve conflict regarding features and requirements• Analyze and decide complaints and charms • Achieve commitments with and motivate development teams, assist development teams in attaining maximum effective sustainable pace for development• Ensure quality by evaluating results of iterations and either approve/ accept or reject results based on DONEness criteria• Support effort estimations of development teams• Analyze change request entries and prioritize with other product backlog items• Coordinate cross-feature-area development with peers to facilitate prioritized product development• Deliver input for project management• Support roll-out of the system, presentation, workshops, training for sales and engineeringWhat do I need to know to qualify for this job?Qualification: A Bachelors / masters degree in engineering and / or MCA or equivalent.Work Experience: 12 to 15 yearsDesired Knowledge & Experience:• Healthcare market. Product knowhow and customer understanding• Sound knowledge of Clinical Workflows and Healthcare IT, especially in the area of Cardiology.• Healthcare Industry standards like DICOM, IHE and HL7• Good understanding of software systems categorized as Medical Device• Basic understanding of Legal regulations and standards applicable for medical devices, affecting safety aspects(i.e. FDA 21CFR820QSR, ISO 13485)• Exposure to agile methodology• Good programming skills & should have worked for a majority of time in software programming roles.• Thorough experience in Requirements Engineering, Usability Engineering and feature definition activities.• Product Lifecycle Management & Software development cycle experience• Integration with different 3rd party applications.What experience do I need to have?• Professional: Several years of experience in the medical device/ healthcare industry (e.g. as a Product Owner, System Engineer, System Analyst, Technology Lead, Lead Architect etc.), expertise in clinical and radiological workflows, experience in image processing. Several years of experience in IT product or solution business. Coming from a software development background is a must.• Project / Process: Several years of experience in requirements engineering and SW development. Ideally, IT integration experience. Experience in agile development projects, preferably in Product Owner role.• Leadership: Experience with managing internationally staffed teams, management and balancing of different stakeholder expectations, management of product definitions. Ideally several years experience in technical leadership role and communicating direction and coaching others.• Intercultural: Experience with international/ intercultural teams, conduction of workshops with international development partners and customers.What else do I need to be strong at?• Self driven and takes Initiatives• Decision making skills• Result orientation• Self motivated and provides motivation and inspiration to the team• Strong Analytical and Problem Solving Skills.• Strong team player and networking skills• Strong written and oral communication skills.• Strong interpersonal skills• Strong customer focusSalary: . Date posted: 04/03/2024 09:24 PM

At Siemens Healthineers, we believe that transformational changes will make it possible to turn today's challenges into opportunities. That is why it is our purpose to enable healthcare providers to increase value. We bring it together - medical devices, healthcare professionals, and patients.To achieve this we are looking for a enthusiastic developer with the below requirements:•Understanding and analyzing the requirements of the project.•Ability to suggest possible solutions for the given requirements•Realize the requirements and implement it with highest quality and on time.•Creation and implementation of unit, integration, sub-system and system level test cases.•Validation of the implemented featuresGeneral Experience & Skill Set•BE / B.Tech / MCA / ME / M.Tech with 3-7 years of experience•Strong OOPS programming skills•Experience with Healthcare will be an added advantage•Hands-on experience on developing enterprise level Cloud applications using web-services (WCF/WebAPI), Windows Azure programming and deployment, medical domain knowledge (DICOM etc), Unit-testing frameworks, Agile processes, Design patterns•Hands-on experience in modern web-development using .Net core, C#, Angular2+, Javascript, HTML5, CSS•Conversant with Continuous Delivery practices like - TDD, BDD and Pair programming•Ability to work as an individual contributor•Flair to learn new technologies and thrive in an agile environment•Conversant with typical software development processes / methodologies and exposure in working with multi-site global teams.Salary: . Date posted: 04/04/2024 02:10 PM

DESCRIPTIONAs part of the world's largest online store, Amazon's Restricted Products (RP) team protects Amazon customers from products that are illegal or otherwise restricted by Amazon policies. As a Risk Manager on the team, you'll help design, create and deploy internal tools and tech that keep Amazon a safe place to shop. You'll partner with multiple stakeholders to make sure that Amazon employees have the best user-facing tools and help us stay up-to-date with emerging threats and risks in the e-commerce space. Given the size of our store, you'll have a unique opportunity to operate at unmatched scale, making decisions that impact tens of millions of products and Amazon shoppers worldwide In this role you will: • Define operational strategies for intricate business and program needs, incorporating inputs and driving alignment across world wide teams. • Manage the delivery of complex initiatives across various teams, components of which include data analysis, operationalizing and scaling new processes, and catalog classification • Develop and maintain metrics and reporting to monitor risks, program health, and initiative progress • Conduct risk assessments of existing controls and recommend solutions to address identified risks such as developing region-specific abuse prevention processes, tools, and policies • Identifies potential areas of compliance vulnerability and risk; develops/implements corrective action plans for resolution of problematic issues, and provides general guidance on how to avoid or deal with similar situations in the futureAbout the teamThe Restricted Products Worldwide Compliance Health team acts as "the pulse of Restricted Products" by developing process to reduce risk on our catalog, driving risk metrics, standardization and simplification of process, across all teams in RP based on gaps or defects identified in a given process, re-evaluation of standard operating procedures and targeting new signals. WWCH team members are single threaded leaders with accountability to identify gaps and reduce risk on our catalog. The team prioritizes risk reduction and works with global program leads, to setup and standardize processes for risk reduction.We are open to hiring candidates to work out of one of the following locations:Bangalore, KA, INDBASIC QUALIFICATIONS• 2+ years experience in program or project management • Experience using data and metrics to drive improvements • Experience defining requirements, facilitating progress and identifying blockers. • Experience implementing repeatable processes and driving automation or standardization • Experience owning program strategy and end to end delivery • Experience with improving team efficiency and improving processes. • Bachelor's Degree or Equivalent ExperiencePREFERRED QUALIFICATIONS• Education or certification background such as; Six Sigma, Lean Techniques, or Project Management Professional (PMP) • Demonstrated experience and success in Operations oriented projects. • Demonstrated success working cross functionally with tech and non-tech teams • Ability to work independently and demonstrate sound judgment in ambiguous situations • Ability to define Program Management strategies; ability to deliver independently, with limited guidance and structure. • Experience working with multiple stakeholders. • Experience with commitment towards goals and outcomes and to ensure Customer Experience metrics are maintained • Experience in writing/ amending SQL queries will be an added advantageSalary: . Date posted: 03/19/2024 09:17 AM