269 Psur Jobs - Page 4

Collaborate with cross-functional teams to ensure seamless clinical development processes. Develop and implement effective monitoring strategies to enhance patient outcomes. Conduct thorough data analysis and interpretation to inform medical decisions. Provide expert guidance on clinical trial design, methodology, and statistical analysis. Ensure compliance with regulatory requirements and industry standards. Foster strong relationships with stakeholders, including investigators, sponsors, and patients. Job Requirements Strong understanding of clinical development principles, practices, and regulations. Excellent analytical, problem-solving, and communication skills. Ability to work effectiv...

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...

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 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...

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 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 ...

We are looking for a highly skilled Regulatory Medical Writer with 1 to 6 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in regulatory affairs and medical writing, with excellent communication and analytical skills. Roles and Responsibility Develop high-quality regulatory documents, including clinical study reports, marketing authorizations, and other related materials. Collaborate with cross-functional teams, including regulatory affairs, product development, and clinical operations. Conduct thorough reviews of regulatory documents to ensure accuracy, completeness, and compliance with regulatory requirements. Stay up-to-date with changing r...

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 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 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 issues. Develop and maintain strong relationships with customers and stakeholders. Stay updated with industry trends and developments in medical services. Analyze data and metrics to improve medical enquiry monitoring processes. Job Requirements Strong knowledge of medical terminology and procedures. Excellent communication and interpersonal skills. Ability to work in a fast-paced environment and meet deadlines. Strong problem-solving and analytical skills. ...

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...

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...

Roles and Responsibility Develop and implement effective monitoring strategies to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and mitigate potential risks and issues. Conduct thorough reviews of clinical trial data to ensure accuracy and completeness. Provide expert guidance on medical aspects of clinical development projects. Ensure timely and effective communication with stakeholders regarding project progress and updates. Identify areas for process improvement and implement changes to increase efficiency. Job Requirements Strong understanding of clinical development principles and regulations. Excellent analytical and problem-solving...

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...