610 Case Processing Jobs - Page 9

Roles and Responsibility Manage and oversee clinical study data management activities, ensuring compliance with regulatory requirements. Develop and implement effective data management plans to ensure data quality and integrity. Collaborate with cross-functional teams to identify and resolve data-related issues. Conduct regular audits to ensure adherence to data management standards. Provide training and support to junior staff members on data management best practices. Ensure timely delivery of high-quality results while maintaining attention to detail. Job Requirements Strong understanding of clinical trial conduct, including protocol development and site monitoring. Experience with data m...

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...

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 Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review meetings with internal and external stakeholders. Job Requirements Strong knowledge of clinical trials, including design, conduct, and reporting. Excellent communication...

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 Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 4 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols, procedures, and study designs. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate in protocol development and review processes. Job Requirements Minimum 2 years of experience in clinical trials or a related field. Strong knowledge of clinical trial principles, practices, and regulation...

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 ...

Main responsibilities: Responsible for research and authoring of scientific response documents under the direction of the Global Medical Information (GMI) team in support of global and local medical information activities. Responsible for the execution of activities as required in alignment with GMI colleagues. Achieved through a combination of product knowledge, along with editing, writing, and document management proficiency. Essential Job duties and responsibilities: Conducts literature searches and reviews, and extracts/summarizes complex data from the scientific literature. Generates evidence-based, accurate, current, and fair-balanced summaries of data for the creation/maintenance of s...

We are looking for a highly skilled and experienced Clinical Trial Medical Advisor to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 32 years of experience in the IT Service & Consulting industry. Roles and Responsibility Collaborate with cross-functional teams to ensure successful clinical trial execution. Provide medical expertise and guidance on clinical trial protocols and procedures. Develop and maintain relationships with key stakeholders, including investigators, sponsors, and regulatory agencies. Conduct site feasibility assessments and provide recommendations for study locations. Ensure compliance with regulatory requirements and company policies. Participate ...

We are looking for a highly skilled and experienced Clinical Research Medical Advisor to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. The ideal candidate will have 2-49 years of experience. Roles and Responsibility Collaborate with cross-functional teams to design and implement clinical research studies. Provide medical expertise and guidance on study protocols, case report forms, and investigational reports. Develop and maintain relationships with investigators, site staff, and other stakeholders. Review and approve study-related documents, including protocols, informed consent forms, and case report forms. Ensure complian...

We are looking for a highly skilled Regulatory Medical Writer with 3 to 8 years of experience to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. Roles and Responsibility Develop high-quality regulatory documents, including clinical trial applications, marketing authorizations, and other related submissions. Collaborate with cross-functional teams to ensure compliance with regulatory requirements and company standards. Conduct thorough research and analysis of regulatory guidelines, laws, and regulations to inform document content. Create clear, concise, and well-structured documents that meet regulatory requirements. Review an...

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...

We are looking for a highly skilled Medical Writer with 3 to 8 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in medical writing and excellent communication skills. Roles and Responsibility Develop high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay updated with the latest developments in the field. Edit and review written content for clarity, grammar, and style. Ensure compliance with regulatory requirements and industry standards....

We are looking for a highly skilled Medical Writer with 2 to 5 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in medical writing and excellent communication skills. Roles and Responsibility Develop high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay up-to-date with industry developments. Edit and proofread written content for clarity, grammar, and punctuation. Meet deadlines and deliver high-quality work under tight timelines. Parti...

Roles and Responsibility Develop comprehensive, accurate, and engaging medical documents, including reports, articles, and presentations. Collaborate with cross-functional teams to ensure timely delivery of projects and meet deadlines. Conduct thorough research on various medical topics to stay updated with industry developments. Edit and proofread written content for clarity, grammar, and punctuation accuracy. Participate in brainstorming sessions to generate new ideas and concepts for content creation. Stay current with industry trends and advancements in medicine and healthcare. Job Requirements Minimum 5 years of experience in medical writing or a related field. Strong understanding of m...

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 Manage and oversee the collection, review, and reporting of clinical trial data. Develop and implement effective data management plans and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct quality control checks on data accuracy and integrity. Provide training and support to staff members on data management best practices. Ensure timely delivery of high-quality data products to stakeholders. Job Requirements Strong knowledge of Good Clinical Practice (GCP) principles and regulations. Experience with clinical trial databases and data management systems. Excellent analytical and problem-solving skills with at...

Roles and Responsibility Manage and oversee the collection, review, and reporting of clinical trial data. Develop and implement effective data management plans and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Conduct quality control checks on data accuracy 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 Good Clinical Practice (GCP) principles and regulations. Experience with clinical trial databases and data management systems. Excellent analytical and problem-solving skills with attention ...

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 cross-functional teams to develop and implement 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 expert guidance on medical matters related to project development. Job Requirements Strong understanding of medical terminology and concepts. Excellent analytical and problem-solving skills. Ability to work effectively in a fast-paced environment a...

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 high-quality written materials for various medical publications, including clinical trials and research studies. Collaborate with cross-functional teams to ensure accurate and timely delivery of written content. Conduct thorough research on medical topics and stay up-to-date with industry developments. Edit and proofread written content for clarity, grammar, and punctuation. Meet deadlines and deliver high-quality work under tight timelines. Participate in quality control processes to ensure consistency and accuracy in written materials. Job Requirements Strong knowledge of medical terminology and concepts, including anatomy, physiology, and pharmacology. Exc...