1037 Argus Jobs - Page 11

Roles and Responsibility Coordinate regulatory submissions with cross-functional teams to ensure timely and accurate delivery. Develop and maintain relationships with regulatory authorities and stakeholders. Prepare and review regulatory documents, including applications, reports, and other submissions. Ensure compliance with regulatory requirements and guidelines. Collaborate with internal teams to resolve issues related to regulatory submissions. Maintain accurate records of regulatory submissions and interactions. Job Requirements Minimum 2 years of experience in regulatory submissions or a related field. Strong knowledge of regulatory requirements and guidelines. Excellent communication ...

Roles and Responsibility Conduct clinical trials to ensure compliance with regulatory requirements and company standards. Collaborate with cross-functional teams to design, implement, and monitor clinical trial protocols. Develop and maintain relationships with investigators, site staff, and other stakeholders to ensure successful study execution. Review and approve clinical trial protocols, informed consent forms, and other study-related documents. Ensure timely and accurate reporting of clinical trial data to relevant authorities. Participate in quality assurance activities to ensure high-quality deliverables. Job Requirements Minimum 2 years of experience in clinical trials, preferably in...

Roles and Responsibility Conduct thorough medical reviews of device-related documents to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to device safety and efficacy. Develop and maintain expertise in medical devices and equipment, including their design, development, and testing. Analyze data from various sources, such as clinical trials and patient reports, to inform device-related decisions. Provide guidance on best practices for medical review processes and procedures. Stay up-to-date with industry developments and emerging trends in medical devices and technology. Job Requirements Strong understanding of med...

Roles and Responsibility Conduct thorough medical reviews of patient data to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and implement effective strategies to improve medical review processes and outcomes. Provide expert guidance on medical review best practices to junior team members. Stay up-to-date with changing regulations and guidelines related to medical review. Participate in quality improvement initiatives to enhance medical review efficiency and effectiveness. Job Requirements Strong knowledge of medical terminology, anatomy, and physiology. Excellent analytical...

Roles and Responsibility Conduct thorough medical reviews of patient data to ensure accuracy and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and implement effective strategies to improve medical review processes and outcomes. Provide expert guidance on medical review best practices to junior team members. Stay up-to-date with changing regulations and guidelines related to medical review. Participate in quality improvement initiatives to enhance medical review efficiency and effectiveness. Job Requirements Strong knowledge of medical terminology, anatomy, and physiology. Excellent analytical...

Roles and Responsibility Conduct thorough medical reviews of device-related documents, including clinical trial protocols and study reports. Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards. Develop and maintain expertise in medical devices and equipment, staying up-to-date with new technologies and advancements. Provide guidance and support to junior staff members on medical review processes and procedures. Participate in quality improvement initiatives to enhance the efficiency and effectiveness of medical review activities. Communicate complex technical information effectively to non-technical stakeholders through written rep...

Roles and Responsibility Publish and submit regulatory documents to relevant authorities. Ensure compliance with regulatory requirements and guidelines. Coordinate with cross-functional teams to prepare and review regulatory submissions. Maintain accurate records of regulatory submissions and correspondence. Stay updated with changes in regulatory requirements and implement updates accordingly. Collaborate with internal stakeholders to ensure timely submission of regulatory documents. Job Requirements Minimum 3 years of experience in regulatory submissions or a related field. Strong knowledge of regulatory requirements and guidelines. Excellent communication and coordination skills. Ability ...

Roles and Responsibility Conduct thorough medical reviews of device data to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to device safety and efficacy. Develop and maintain comprehensive reports detailing findings and recommendations. Stay up-to-date with industry trends and developments in medical devices and technology. Provide training and guidance to junior staff members on medical review procedures. Participate in quality improvement initiatives to enhance processes and outcomes. Job Requirements Strong understanding of medical terminology and regulations governing medical devices. Excellent analytical and...

Roles and Responsibility Conduct thorough medical reviews of device-related documents to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve issues related to medical review. Develop and maintain expertise in medical review processes and procedures. Provide guidance and support to junior team members on medical review best practices. Stay up-to-date with changing regulations and guidelines related to medical review. Participate in quality improvement initiatives to enhance medical review processes. Job Requirements Strong understanding of medical terminology and regulatory requirements. Experience with medical review software and sy...

Roles and Responsibility Manage and publish regulatory submissions, ensuring compliance with relevant laws and regulations. Coordinate with cross-functional teams to ensure timely submission of regulatory documents. Develop and maintain relationships with regulatory authorities and other stakeholders. Stay updated on changes in regulatory requirements and implement necessary updates. Ensure accurate and high-quality content in all regulatory submissions. Collaborate with internal teams to resolve issues related to regulatory submissions. Job Requirements Strong knowledge of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independently...

Roles and Responsibility Conduct thorough medical reviews of device-related documents, including clinical trial protocols and study reports. Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards. Develop and maintain expertise in medical devices and equipment, staying up-to-date with new technologies and advancements. Provide guidance and support to junior staff members on medical review processes and procedures. Participate in quality improvement initiatives to enhance the efficiency and effectiveness of medical review activities. Communicate complex technical information effectively to non-technical stakeholders through written rep...

We are looking for a highly skilled Medical Reviewer to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. The ideal candidate will have 3-6 years of experience and be responsible for reviewing medical records and ensuring compliance with regulatory requirements. Roles and Responsibility Conduct thorough reviews of medical records, including patient histories and treatment plans. Ensure compliance with regulatory requirements, such as FDA guidelines and GCP protocols. Collaborate with cross-functional teams, including clinical operations and data management. Develop and maintain expertise in medical terminology, regulations, and ...

Requirement : This role is responsible for overall development, configuration and maintenance of Argus Safety Experience in Argus Console and Argus Administration activities Experience on configuration of reporting destinations, reporting rules and configuration of Advance Conditions and Advance Condition Sets based on project requirements Experience in Code Lists, Business Configuration, Access Management and System Configuration Experience in Configuration and providing support to periodic reports - DSUR,PADER,PBRER,CIOMS II Line Listings and X monthly SUSAR Line listings and other adhoc reports based on client needs. Experience in periodic reports in Argus Application ,PV Reports and Orac...

Job Description: Job Overview: We are seeking Quality Assurance testers to join our Digital team. In this role, you will be engaging with our Developers and Delivery Leads to perform manual testing across multiple online digital products and later create test suites to complete workflow with automation solutions. Your primary responsibility will be to understand requirements and acceptance criteria to develop test cases. You will also be responsible for leading UAT in collaboration with our Product Owners. Day-to-Day: Getting to familiarize with the features being rolled out in Production releases. Create & execute detailed, comprehensive, and well-structured test plans and test cases for en...

Job Description: About the Job: The Cybersecurity Risk Management team is part of Chief Security Office (CSO) and responsible for managing multiple teams that facilitate external audits, internal audits, analyze policy exceptions, conduct risk assessments, and run enforceable governance across processes. They work closely with the AT&T Technology Services (ATS) teams and Technology Risk Management (TRM) teams and other CSO teams to ensure the effective and efficient GRC processes. Below are the key responsibilities of the Senior Specialist – Audit Management (ISO 27001) position: Develop and maintain audit plans to ensure all activities supporting the annual internal and external ISO 27001 a...

Job Description: About the Job: The Cybersecurity Risk Management team is part of Chief Security Office (CSO) and responsible for managing multiple teams that facilitate external audits, internal audits, analyze policy exceptions, conduct risk assessments, and run enforceable governance across processes. They work closely with the AT&T Technology Services (ATS) teams and Technology Risk Management (TRM) teams and other CSO teams to ensure the effective and efficient GRC processes. Below are the key responsibilities of the Specialist – Audit Management (ISO 27001) position: Develop and maintain audit plans to ensure all activities supporting the annual internal and external ISO 27001 audits a...

Position Specification – Manager, Real Estate Debt Valuation Scope And Responsibilities Conduct valuations of real estate private credit as part of the quarterly or monthly valuation process. Assist with verifying the completeness of daily valuation process and escalate timely when additional review and approval is required. Perform reconciliations across valuation models, accounting records, and multiple data sources. Lead specific projects: Analyze and determine scope of work, gather data, and prepare / review valuation models, ensuring high quality and timely delivery. Prepare and present valuation results: Communicate findings clearly and concisely to team leaders and stakeholders. Analy...

About The Role About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire a...

About The Role About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire a...

About The Role Project Role : Tech Delivery Subject Matter Expert Project Role Description : Drive innovative practices into delivery, bring depth of expertise to a delivery engagement. Sought out as experts, enhance Accentures marketplace reputation. Bring emerging ideas to life by shaping Accenture and client strategy. Use deep technical expertise, business acumen and fluid communication skills, work directly with a client in a trusted advisor relationship to gather requirements to analyze, design and/or implement technology best practice business changes. Must have skills : Oracle Argus Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 year...

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Oracle Argus Good to have skills : NAMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will engage in the design, construction, and configuration of applications tailored to fulfill specific business processes and application requirements. Your typical day will involve collaborating with team members to understand project needs, developing innovative solutions, and ensuring that applications function seamlessl...

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Oracle Argus Good to have skills : NAMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will engage in the design, construction, and configuration of applications tailored to fulfill specific business processes and application requirements. Your typical day will involve collaborating with team members to understand project needs, developing innovative solutions, and ensuring that applications function seamlessl...

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Sr Analyst Qualifications: Bachelor of Pharmacy Years of Experience: 5 to 8 years About Accenture Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. Visit us at www.accenture.com What would you do You will be align...

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and de...

Argus is where smart people belong and where they can grow. We answer the challenge of illuminating markets and shaping new futures. What We’re Looking For Argus is a leading provider of insights, price indexes and consulting to the global energy industry. Companies in 140 countries as well as multilaterals like the International Energy Agency (IEA) use Argus data to index physical trade and as benchmarks in financial derivative markets as well as for analysis and planning purposes. We also have a burgeoning commodities markets consulting division that offers clients insights into the evolving markets and the opportunities that these changes present. This division uses industry best practice...