610 Case Processing Jobs - Page 10

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 Publish regulatory submissions to relevant authorities, ensuring compliance with required standards and regulations. Collaborate with cross-functional teams to prepare and review regulatory documents, including applications, reports, and other submissions. Develop and maintain relationships with regulatory bodies and respond to queries related to regulatory submissions. Stay updated on changes in regulatory requirements and implement necessary updates to ensure compliance. Review and edit regulatory documents for accuracy, completeness, and adherence to company policies. Coordinate with internal stakeholders to gather information and support for regulatory submission...

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 Develop high-quality medical content for various platforms, including reports and presentations. Conduct thorough research on medical topics and stay updated with the latest developments. Collaborate with cross-functional teams to ensure accurate and consistent messaging. Create engaging and informative content that meets the needs of diverse audiences. Edit and review content for clarity, grammar, and accuracy. Stay current with industry trends and best practices in medical writing. Job Requirements Strong understanding of medical terminology and concepts. Excellent writing and communication skills. Ability to work independently and as part of a team. Proficient in ...

Roles and Responsibility Conduct thorough reviews of medical records, including patient histories and treatment plans. Analyze data to identify trends and patterns that inform medical decisions. Collaborate with healthcare professionals to develop effective treatment plans. Develop and maintain accurate and up-to-date documentation of review findings. Stay current with industry developments and advancements in medical research. Provide training and guidance to junior staff members on medical review procedures. Job Requirements Strong knowledge of medical terminology and concepts. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment with mul...

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...

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 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 on new technologies and trends. Provide guidance and support to junior staff members, sharing knowledge and best practices. Participate in quality improvement initiatives, identifying areas for process enhancement and implementing changes. Maintain accurate records of all interactions with clients, including phone calls, emails, and written correspondence. Jo...

Roles and Responsibility Conduct thorough medical reviews of device-related documents, including clinical trial protocols and 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 prese...

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 Manage and oversee the collection, review, and reporting of clinical trial data. Develop and implement effective data management plans to ensure compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data-related issues. Conduct regular audits to ensure data quality and integrity. Provide training and support to staff on data management best practices. Ensure timely delivery of high-quality data products to stakeholders. Job Requirements Strong knowledge of clinical study protocols and regulations. Experience with data management systems and software. Excellent analytical and problem-solving skills. Ability to work ef...

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 ...

Skill required: Pharmacovigilance Services - Safety Writing 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 aligned with our Life Sciences R&D ...

About The Role Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 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...

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...

Project Role : Business Process Architect Project Role Description : Analyze and design new business processes to create the documentation that guides the implementation of new processes and technologies. Partner with the business to define product requirements and use cases to meet process and functional requirements. Participate in user and task analysis to represent business needs. Must have skills : SAP PP Production Planning & Control Discrete Industries Good to have skills : NAMinimum 12 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Business Process Architect, you will analyze and design new business processes to create the doc...