1037 Argus Jobs - Page 9

End to end Testing related activities including requirement analysis, Test data and test case creation, execution (IQ,OQ,PQ), review of test results and defect management. Knowledge working with PV systems like Argus safety Experience in testing PV processes, facilitating UAT and PQ execution Organizing, monitoring defect management process handling changes and conducting regression tests. Work in lieu of System Managers/Validation Responsible and QA for Testing document deliverables. Coordinate with Line of business across various locations around the world Ensure quality of deliverables are met and in alignment with the stakeholder expectations Help achieve Productivity, Quality, Timelines...

Job Summary: We are seeking an experienced and detail-oriented Argus Modeling experienced to join our team. The candidate will be responsible for providing financial analysis and modeling support using Argus software for our commercial real estate portfolio for Middle East Team. The ideal candidate should have a strong financial background, excellent analytical skills, and proficiency in working with Argus Enterprise software. Responsibilities: Develop accurate and comprehensive financial models using Argus Enterprise software for existing and potential commercial real estate investments. Support to the Middle East team and working directly with the onsite team. Conduct detailed cash flow an...

About The Role Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the worlds leading biopharma companies bring their vision to li...

Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally Main responsibilities: The overall purpose and main responsibilities are listed below: Responsible for project management support to the scientific writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases Initiate and amend submission based on c...

Main responsibilities: The overall purpose and main responsibilities are listed below: Responsible for project management support to the scientific writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases. Initiate and amend submission based on comments (as required). Support the writer with internal and external stakeholder communication. Track the delivery of activities (including managing issues and risks) and support follow up. Support required submission, compliance/ approval activities, and ensure compliance with publication processes and end-to-end publication management tools (e.g., iEnvision - previously,...

Salesforce is the global leader in customer relationship management (CRM) software, pioneering the shift to cloud computing and delivering innovative technologies to help companies revolutionize the way they interact with customers. As the fastest growing enterprise software company and recognized for innovation and workplace culture, Salesforce is seeking a Database Cloud Engineer to join the CRM Database Sustaining Engineering Team. **Role Overview:** As a Database Cloud Engineer at Salesforce, you will play a critical role in ensuring the reliability, scalability, and performance of the company's cloud database infrastructure. You will collaborate with various teams to architect and opera...

Contribute to the creation and maintenance of risk management plans & provides support for the effective implementation of Additional Risk Minimisation measures. Safety mailbox and communications management. Support Aggregate Report related activities. Maintenance of PV Awareness and other related Training content. Implementation of Pharmacovigilance Agreements. Individual Case Safety Report (ICSR) related activities, including literature screening, and submissions to local Health Authorities and Ethics Committees. Safety Data Quality activities e. g. PV System Master File maintenance, deviations/CAPA management, other quality control and oversight activities. Compilation of PV-related docum...

Hiring: PLSQL with Argus Expert Location: Bangalore (Hybrid 3 days office) Experience: 6 - 12 years Mandatory Skills: PLSQL, SQL, Oracle Argus Power BI (Good to have) Data Virtualization Tools (Denodo – Preferred) Key Responsibilities: Provide complex query and reporting support using SQL & PL/SQL. Write complex SQL queries for data extraction and analysis. Work with data virtualization tools (Denodo) for seamless data integration. Hands-on experience with Power BI administration & report scheduling. Gather business requirements and translate them into technical specifications. Develop and maintain custom Power BI reports & dashboards. Handle ServiceNow requests & incidents related to Power ...

Hiring for PLSQL with Argus Expert Location: Bangalore (Hybrid 3 days office) Experience: 6 - 12 years Mandatory Skills: PLSQL, SQL, Oracle Argus Power BI (Good to have) Data Virtualization Tools (Denodo Preferred) Note : Immediate to 15 days only who are serving Notice . Key Responsibilities: Provide complex query and reporting support using SQL & PL/SQL. Write complex SQL queries for data extraction and analysis. Work with data virtualization tools (Denodo) for seamless data integration. Hands-on experience with Power BI administration & report scheduling. Gather business requirements and translate them into technical specifications. Develop and maintain custom Power BI reports & dashboard...

*URGENT HIRING* Company Description Argus Consulting (India) is a software consulting service firm specializing in hi-tech technologies, including cloud-based solutions. We are committed to providing innovative, efficient, and secure technology solutions to our clients. Our expertise in cutting-edge technologies allows us to deliver tailored services that meet specific business needs. At Argus Consulting, our goal is to empower our clients through technology-driven growth and efficiency. Role Description This is a contract remote role for an Application Developer (PERL and Python). The Application Developer will be responsible for designing, developing, and maintaining software applications....

Roles and Responsibility Monitor medical enquiries and respond to customer inquiries professionally. Provide excellent customer service and ensure high customer satisfaction. Collaborate with internal teams to resolve medical queries and concerns. Develop and maintain knowledge of medical terminology and procedures. Analyze data and trends to identify areas for improvement in medical enquiry monitoring. Implement process improvements to increase efficiency and productivity. Job Requirements Strong communication and interpersonal skills are essential. Ability to work effectively in a fast-paced environment and prioritize tasks. Basic computer skills and proficiency in Microsoft Office are req...

Roles and Responsibility Coordinate and manage regulatory submissions, ensuring compliance with relevant laws and regulations. Develop and implement effective submission strategies to achieve business objectives. Collaborate with cross-functional teams to ensure timely and accurate submissions. Conduct thorough reviews of submissions to identify areas for improvement. Maintain accurate records of submissions and follow up on pending submissions. Stay updated with changes in regulatory requirements and guidelines. Job Requirements Strong knowledge of regulatory submissions and compliance. Excellent communication and project management skills. Ability to work in a fast-paced environment and me...

Roles and Responsibility Develop and implement effective medical monitoring strategies for clinical trials. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct regular reviews of medical data to identify trends and potential issues. Provide expert guidance on medical aspects of clinical development projects. Ensure timely reporting of medical information to stakeholders. Participate in quality improvement initiatives to enhance medical monitoring processes. Job Requirements Strong understanding of clinical development principles and regulations. Excellent analytical and problem-solving skills. Effective communication and collaboration skills. Ab...

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 study protocols. Provide medical guidance and support to trial participants and their families. Develop and maintain accurate records of patient data and study progress. Participate in quality control and quality assurance activities to ensure high-quality data. Stay updated with industry developments and advancements in medical research. Job Requirements Minimum 2-6 years of experience in clinical trials or related fields. Strong knowledge of clinical trial principles, regulations, and procedures. ...

Roles and Responsibility Publish regulatory submissions on time, ensuring accuracy and compliance with relevant regulations. Collaborate with cross-functional teams to prepare and review regulatory documents. Develop and maintain relationships with regulatory authorities and stakeholders. Stay updated with changes in regulatory requirements and implement necessary updates. Ensure all regulatory submissions meet required standards and quality criteria. Coordinate with internal teams to gather information and support for regulatory submissions. Job Requirements Strong knowledge of regulatory requirements and guidelines. Excellent communication and interpersonal skills. Ability to work independ...

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 and regulatory requirements. Excellent analyti...

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 on new technologies and trends. 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 reports and...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right Thing, Customer Success, Employee Success, and Speed. We're not just any public company – we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors. As a Work Anywhere company, we support your flexibility to work from home or in the office, so you can ...

Conduct thorough medical reviews of devices and their associated documentation. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Develop and maintain expertise in medical terminology and device regulations. Provide guidance on medical aspects of device development and implementation. Stay updated with changing trends and developments in medical technology. Participate in quality improvement initiatives to enhance review processes. Job Requirements Strong understanding of medical terminology and device regulations. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Effective communication and interperso...

Conduct clinical trials to ensure compliance with regulatory requirements and company protocols. Collaborate with cross-functional teams, including data management, biostatistics, and medical writing. Develop and implement study-specific procedures and protocols. Monitor and report adverse events during clinical trials. Ensure timely completion of studies within budget and quality standards. Participate in site monitoring visits and audits. Job Requirements Minimum 2 years of experience in clinical trial management or a related field. Strong knowledge of Good Clinical Practice (GCP) principles and regulations. Excellent communication and interpersonal skills. Ability to work independently an...

Develop and implement aggregate reporting solutions to meet business requirements. Collaborate with cross-functional teams to identify and prioritize reporting needs. Design and maintain complex reports using various reporting tools and technologies. Analyze data to identify trends and patterns, providing insights to stakeholders. Ensure data accuracy and integrity in all reports and dashboards. Provide training and support to end-users on reporting tools and technologies. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Proficiency in designing and developing complex reports using various reporting tools and technologies. Excellent analytical and pr...

Conduct thorough analysis of clinical trial data to identify potential safety concerns. Develop and implement effective safety protocols to mitigate risks associated with medical devices. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Perform risk assessments and provide recommendations for improving patient safety. Monitor and report adverse events related to medical devices. Stay updated with changing regulations and guidelines related to clinical safety. Job Requirements Strong understanding of clinical trials, safety protocols, and regulatory requirements. Experience working with medical devices and their applications. Excellent analytical and ...

Manage and analyze aggregate reporting data to provide insights and recommendations. Develop and implement effective reporting strategies to meet business needs. Collaborate with cross-functional teams to ensure accurate and timely reporting. Identify and resolve issues related to reporting data quality and integrity. Develop and maintain complex reports using various reporting tools and technologies. Provide expert guidance on reporting best practices and standards. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Proficiency in analyzing large datasets and providing actionable insights. Excellent communication and interpersonal skills, with the abi...

Develop and implement effective medical monitoring strategies for clinical trials. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct thorough reviews of medical data to identify trends and potential issues. Provide expert guidance on medical aspects of clinical development projects. Ensure timely reporting of adverse events and other critical information. Participate in quality control activities to maintain high standards of data accuracy. Job Requirements Strong understanding of clinical development principles and practices. Excellent analytical and problem-solving skills, with attention to detail. Effective communication and interpersonal s...

Develop and implement effective medical monitoring strategies for clinical trials. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct thorough reviews of medical data to identify trends and potential issues. Provide expert guidance on medical matters related to clinical development. Ensure timely reporting of adverse events and other safety concerns. Participate in quality control activities to maintain high standards of medical practice. Job Requirements Strong knowledge of clinical development principles and practices. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment. Effective communica...