1037 Argus Jobs - Page 10

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 mitigate risks associated with reporting processes. Develop and maintain relationships with stakeholders to ensure effective communication. Stay up-to-date with industry trends and best practices in aggregate reporting. Job Requirements Strong understanding of aggregate reporting principles and methodologies. Experience with data analysis and interpretation to inform business decisions. Excellent communication and interpersonal skills. Abil...

Roles and Responsibility Collaborate with cross-functional teams to ensure timely and successful clinical development projects. Develop and implement medical monitoring strategies to ensure patient safety and data quality. Conduct thorough reviews of clinical trial data to identify trends and areas for improvement. Provide expert guidance on medical aspects of clinical trials, including protocol development and study conduct. Ensure compliance with regulatory requirements and company policies. Participate in ongoing education and training to stay current with industry developments. Job Requirements Strong understanding of clinical development principles, including FDA regulations and GCP gui...

Roles and Responsibility Publish regulatory submissions according to company guidelines and timelines. Ensure compliance with regulatory requirements and industry standards. Collaborate with cross-functional teams to meet submission goals. Review and edit regulatory documents for accuracy and completeness. Maintain accurate records of submissions and publications. Stay updated with changing regulatory requirements and guidelines. Job Requirements Minimum 2 years of experience in regulatory submissions or a related field. Strong knowledge of regulatory requirements and industry standards. Excellent publishing and communication skills. Ability to work independently and as part of a team. Stron...

Roles and Responsibility 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. Proficient in analyzing large datasets and providing actionable insights. Excellent communication and interperso...

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 244 years of experience in clinical trials or related fields. Strong knowledge of clinical trial principles, regulations, and procedures. ...

As a Database Cloud Engineer at Salesforce, your role is crucial in ensuring the reliability, scalability, and performance of Salesforce's extensive cloud database infrastructure. You will contribute to powering one of the largest SaaS platforms globally. With a DevOps mindset and deep database expertise, you will architect and operate secure, resilient, and high-performance database environments on public cloud platforms like AWS and GCP. Collaboration across various teams will be essential to deliver cloud-native reliability solutions at a massive scale. Key Responsibilities: - Architect and operate resilient, secure, and performant database environments on public cloud platforms - Collabo...

We are currently seeking a Pharmacovigilance Reporting Associate to join our diverse and dynamic team. As a Pharmacovigilance Reporting Associate at ICON, you will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities. You will ensure compliance with regulatory requirements and contribute to the effective management of safety data to support patient safety and regulatory compliance. What You Will Be Doing: Preparing and reviewing safety reports, including periodic safety updates and individual case safety reports, ensuring accuracy and compliance with regulatory standards. Collecting and analyzing adverse event data ...

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, approvals, and other relevant documents. Stay up-to-date 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 effectively in a fast-paced...

Roles and Responsibility Coordinate and prepare regulatory submissions for timely and accurate filing. Develop and maintain relationships with regulatory authorities and stakeholders. Conduct thorough reviews of regulatory documents to ensure accuracy and completeness. Collaborate with cross-functional teams to meet regulatory requirements. Stay updated on changing regulatory requirements and implement necessary changes. Ensure compliance with all relevant laws and regulations. Job Requirements Strong knowledge of regulatory requirements and guidelines. Excellent communication and coordination skills. Ability to work independently and as part of a team. Strong analytical and problem-solving ...

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, approvals, and other related documents. Stay up-to-date 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 effectively in a fast-paced ...

Roles and Responsibility Develop high-quality medical writing content for various reports, including Aggregate Reports. Collaborate with cross-functional teams to ensure timely delivery of projects. Conduct thorough research and analysis to stay updated on the latest developments in Pharmacovigilance. Create engaging and informative content that meets client requirements. Edit and review content for accuracy, clarity, and consistency. Work closely with clients to understand their needs and deliver tailored solutions. Job Requirements Minimum 2 years of experience in medical writing, preferably in Pharmacovigilance or Aggregate Reports. Strong understanding of medical terminology, regulations...

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 customer complaints and concerns. Develop and maintain strong relationships with customers and stakeholders. Analyze customer feedback and suggest improvements to processes and procedures. Ensure compliance with company policies and procedures. Job Requirements Strong communication and interpersonal skills are essential. Ability to work in a fast-paced environment and meet deadlines is required. Excellent problem-solving and analytical skills are necessary. Strong attention to ...

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 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 medical information to stakeholders. Stay updated with changing regulations and guidelines related to medical monitoring. 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. Eff...

Roles and Responsibility Develop high-quality medical writing content for various reports, including aggregate reports on pharmacovigilance. Conduct thorough research and analysis to ensure accuracy and completeness of written content. Collaborate with cross-functional teams to gather information and insights for report development. Create engaging and informative content that meets the needs of stakeholders and audiences. Edit and review content for clarity, grammar, and style. Stay up-to-date with industry trends and developments in pharmacovigilance and aggregate reporting. Job Requirements Minimum 2 years of experience in medical writing, preferably in the IT Service & Consulting industr...

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 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 environ...

Roles and Responsibility Develop high-quality medical reports and documents for pharmaceutical companies. Conduct thorough research on various medical topics related to Pharmacovigilance. Collaborate with cross-functional teams to ensure timely delivery of projects. Analyze complex data sets to identify trends and patterns. Prepare presentations and visualizations to communicate findings to stakeholders. Stay updated with industry developments and regulatory requirements. Job Requirements Minimum 2 years of experience in medical writing, preferably in the IT Service & Consulting industry. Strong knowledge of Pharmacovigilance and Aggregate Reporting. Excellent writing and communication skill...

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 activities to ensure high-quality data and adherence to regulations. Stay updated with changing regulations and guidelines related to clinical trials. Job Requirements Minimum experience in clinical trials or a related field. Strong knowledge of Good Clinical Practice (GCP) principles and regulations. ...

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. Provide medical guidance and support to study participants and investigators. Review and approve clinical trial protocols, informed consent forms, and other study-related documents. Ensure timely completion of clinical trials within budget and according to quality standards. Participate in site monitoring visits and provide feedback on study progress. Job Requirements Minimum 2-3 years of experience in clinical trials or a related field. Strong knowledge of clinical trial r...

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 activities to ensure high-quality data and adherence to regulations. Stay updated with changing regulations and guidelines related to clinical trials. Job Requirements Minimum experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulations. Ex...

Roles and Responsibility Develop high-quality medical writing content for various reports, including aggregate reports on pharmacovigilance. Conduct thorough research and analysis to ensure accuracy and completeness of written content. Collaborate with cross-functional teams to gather information and insights for report development. Create engaging and informative content that meets the needs of stakeholders and audiences. Edit and review content for clarity, grammar, and style. Stay up-to-date with industry trends and developments in pharmacovigilance and aggregate reporting. Job Requirements Minimum 4 years of experience in medical writing, preferably in the IT Service & Consulting industr...

Roles and Responsibility Monitor and analyze medical data to identify trends and patterns. Develop and implement effective medical monitoring systems and processes. Collaborate with cross-functional teams to ensure seamless communication and coordination. Provide exceptional customer service and support to clients and stakeholders. Stay updated with industry developments and advancements in medical technology. Identify and mitigate potential risks and issues in medical monitoring operations. Job Requirements Strong understanding of medical terminology and concepts. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment and prioritize tasks. E...

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 clinical trial data to ensure compliance with regulatory requirements. Analyze and interpret complex medical information to identify trends and patterns. Collaborate with cross-functional teams to develop and implement effective medical strategies. Develop and maintain detailed documentation of medical review processes and findings. Stay up-to-date with changing regulations and guidelines related to medical review. Provide expert guidance on medical matters to junior team members. Job Requirements Strong understanding of clinical research principles and practices. Proficient in data analysis and interpretation using statistical too...

Position Summary The Safety Specialist I is an integral part of the safety team at Precision and performs all aspects of the collection, processing, and reporting of individual cases safety reports (ICSR) for clinical trials and/or post-marketing safety programs. Essential functions of the job include but are not limited to: Process ICSRs according to Standard Operating Procedures (SOPs) and project/program- specific safety plans Triages ICSRs, evaluates ICSR data for completeness, accuracy, and regulatory report ability Enters data into Argus Safety Database Code events, medical history, concomitant medications and tests. Draft case narratives Assesses information to be queried and follows ...

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 products and services. Analyze customer feedback and suggest improvements. Maintain accurate records of customer interactions and transactions. Job Requirements Strong communication and interpersonal skills are essential. Ability to work in a fast-paced environment and meet deadlines. Excellent problem-solving and analytical skills are required. Strong attention to detail and organizational skills are neces...