329 Inform Jobs - Page 6

Roles and Responsibility Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code that meets client specifications and industry standards. Troubleshoot and resolve technical issues related to Veeva EDC clinical programming. Provide training and support to clients on the use of Veeva EDC clinical programming tools. Participate in the development of best practices and standards for Veeva EDC clinical programming. Job Requirements Strong understanding of Veeva EDC clinical programming principles and methodologies. Experience working with var...

Roles and Responsibility Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain high-quality code that meets client specifications and industry standards. Troubleshoot and resolve technical issues related to Veeva EDC clinical programming. Provide training and support to clients on the use of Veeva EDC clinical programming tools. Stay up-to-date with industry trends and emerging technologies in Veeva EDC clinical programming. Job Requirements Strong knowledge of Veeva EDC clinical programming principles and practices. Experience working with IT Service &...

Roles and Responsibility Design, develop, and implement clinical trial data management systems using Veeva EDC. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Develop and maintain high-quality, accurate, and timely clinical trial data. Troubleshoot and resolve issues related to clinical data management and reporting. Ensure compliance with regulatory requirements and industry standards. Participate in project planning, execution, and delivery to meet business objectives. Job Requirements Strong knowledge of Veeva EDC and its applications in clinical trials. Experience working in the IT Service & Consulting industry, prefe...

We are looking for a skilled Veeva EDC Clinical Programmer with 2 to 7 years of experience to join our team in Mumbai. The ideal candidate will have a strong background in IT Service & Consulting, particularly in clinical programming using Veeva EDC. Roles and Responsibility Design, develop, and implement clinical trial data management systems using Veeva EDC. Collaborate with cross-functional teams to ensure seamless integration of clinical data into the development process. Develop and maintain high-quality, accurate, and timely clinical trial data. Troubleshoot and resolve issues related to clinical data management and reporting. Ensure compliance with regulatory requirements and industry...

We are looking for a skilled EDC Programmer to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 1-8 years of experience in the IT Service & Consulting industry. Roles and Responsibility Design, develop, and implement electronic data capture systems. Collaborate with cross-functional teams to identify business requirements and develop solutions. Develop and maintain technical documentation for EDC systems. Troubleshoot and resolve issues related to EDC system implementation. Ensure compliance with industry standards and regulations. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong understanding of electronic data captur...

We are looking for a skilled Clinical Data Manager to join our team at Gratitude India Manpower Consultants Pvt. Ltd., located in the IT Service & Consulting industry. The ideal candidate will have 1-5 years of experience and a strong background in clinical data management. Roles and Responsibility Manage and oversee the development, implementation, and maintenance of clinical databases. Ensure data quality, accuracy, and compliance with regulatory requirements. Collaborate with cross-functional teams to design and implement data-driven solutions. Develop and maintain data standards, guidelines, and best practices. Provide training and support to staff on data management systems. Identify an...

We are looking for a highly skilled and experienced Clinical Data Reconciliation Specialist to join our team at Gratitude India Manpower Consultants Pvt. Ltd., an IT Service & Consulting company based in [location to be specified]. The ideal candidate will have 4-6 years of experience in clinical data reconciliation. Roles and Responsibility Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies to meet project requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Analyze and report on data reconciliation results, identifying trends and areas for imp...

We are looking for a highly skilled and experienced Clinical Data Reconciliation Specialist to join our team at Gratitude India Manpower Consultants Pvt. Ltd., an IT Service & Consulting company based in [location to be specified]. The ideal candidate will have 3-4 years of experience in clinical data reconciliation. Roles and Responsibility Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies to meet project requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies. Analyze and report on data reconciliation results, identifying trends and areas for imp...

We are looking for a highly skilled and experienced Clinical Data Reconciliation Specialist to join our team at Gratitude India Manpower Consultants Pvt. Ltd., an IT Service & Consulting company based in [location to be specified]. The ideal candidate will have 5-10 years of experience in clinical data reconciliation. Roles and Responsibility Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies and procedures. Collaborate with cross-functional teams to identify and resolve data discrepancies. Analyze and interpret complex data sets to identify trends and patterns. Develop and maintain docume...

We are looking for a skilled Clinical Data Manager with expertise in Veeva EDC to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in the IT Service & Consulting industry and 2-7 years of experience. Roles and Responsibility Manage and oversee clinical 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 staff on data manageme...

We are looking for a skilled Clinical Data Manager with expertise in Veeva EDC to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in clinical data management and experience working with IT Service & Consulting companies. Roles and Responsibility Manage and oversee the development, implementation, and maintenance of clinical databases using Veeva EDC. Ensure data quality, integrity, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and prioritize data management needs. Develop and implement data management plans and procedures. Conduct regular audits and reviews of data management ...

We are looking for a skilled Clinical Data Manager with expertise in Veeva EDC to join our team at Gratitude India Manpower Consultants Pvt. Ltd. The ideal candidate will have a strong background in clinical data management and experience working with IT Service & Consulting companies. Roles and Responsibility Manage and oversee the development, implementation, and maintenance of clinical databases using Veeva EDC. Ensure data quality, integrity, and compliance with regulatory requirements. Collaborate with cross-functional teams to ensure seamless integration of clinical data into larger systems. Develop and implement data management plans, procedures, and standards. Conduct regular audits ...

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 development and implementation of clinical data management systems. Ensure compliance with regulatory requirements and industry standards for clinical data management. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and maintain data quality control processes to ensure accuracy and integrity of clinical data. Provide training and support to staff on clinical data management systems and procedures. Analyze and resolve complex data-related issues and discrepancies. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with Veeva EDC is highly desirable. ...

Roles and Responsibility Develop high-quality regulatory documents, including clinical trial applications, marketing authorizations, and periodic safety update reports. Collaborate with cross-functional teams, including regulatory, clinical, and product development, to ensure compliance with regulatory requirements. Conduct thorough reviews of regulatory documents to ensure accuracy, completeness, and adherence to company standards. Stay up-to-date with changing regulatory requirements and industry trends to improve document quality and compliance. Provide training and guidance to junior writers on regulatory affairs and medical writing best practices. Participate in the development of new r...

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 Manage and oversee the clinical data reconciliation process to ensure accuracy and quality. Develop and implement effective data reconciliation strategies to meet business objectives. Collaborate with cross-functional teams to identify and resolve data discrepancies. Analyze and report on data reconciliation metrics to stakeholders. Ensure compliance with regulatory requirements and company policies. Continuously monitor and improve the data reconciliation process to enhance efficiency. Job Requirements Strong understanding of clinical data management principles and practices. Experience with data reconciliation tools and technologies. Excellent analytical and proble...

Roles and Responsibility Design, develop, and implement electronic data capture systems. Collaborate with cross-functional teams to identify business requirements and develop solutions. Develop and maintain high-quality code using various programming languages. Troubleshoot and resolve technical issues efficiently. Participate in code reviews and contribute to improving overall code quality. Stay updated with industry trends and emerging technologies. Job Requirements Strong understanding of electronic data capture systems and their applications. Proficiency in programming languages such as Java or Python. Experience with database management systems and querying languages. Excellent problem-...

Roles and Responsibility Manage and oversee the development, implementation, and maintenance of clinical databases. Ensure data quality, accuracy, and compliance with regulatory requirements. Collaborate with cross-functional teams to design and implement data-driven solutions. Develop and maintain data standards, guidelines, and best practices. Provide training and support to staff on data management systems. Identify and mitigate risks associated with data management. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with clinical trial conduct and regulatory requirements. Excellent communication and interpersonal skills. Ability to work eff...

Roles and Responsibility Design, develop, and implement clinical data programming solutions using R/SQL. Collaborate with cross-functional teams to ensure accurate and timely delivery of projects. Develop and maintain complex databases and data systems. Write efficient and well-documented code. Troubleshoot and resolve technical issues related to clinical data programming. Participate in code reviews and contribute to improving overall code quality. Job Requirements Strong knowledge of R/SQL and its applications in clinical data programming. Experience working with large datasets and developing scalable solutions. Excellent problem-solving skills and attention to detail. Ability to work coll...

Roles and Responsibility Design, develop, and maintain clinical databases using R/SQL. Collaborate with cross-functional teams to ensure data quality and integrity. Develop and implement data validation and verification processes. Troubleshoot and resolve data-related issues efficiently. Ensure compliance with regulatory requirements and industry standards. Participate in the development of new systems and technologies. Job Requirements Strong knowledge of R/SQL and clinical data programming principles. Experience working with large datasets and complex data structures. Excellent problem-solving skills and attention to detail. Ability to work collaboratively in a team environment. Strong com...

About The Role Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Associate Manager Qualifications: BE/BTech/BSc Years of Experience: 10 to 14 years Language - Ability: English(Domestic) - Intermediate 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...

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 : Web Developer Project Role Description : Design, build and test web-based applications for various site components and edit site content. Document technical designs and specifications. Research and incorporate updated content for websites. Must have skills : Infor M3 Process Manufacturing & Distro Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time educationAbout The Role & Summary :We are seeking an experienced Team Lead with specialized expertise in Infor M3 Manufacturing and Distribution and additional knowledge on Finance Management and Migration to join our team for an ongoing migration project ...

Project Role : Technology Support Engineer Project Role Description : Resolve incidents and problems across multiple business system components and ensure operational stability. Create and implement Requests for Change (RFC) and update knowledge base articles to support effective troubleshooting. Collaborate with vendors and help service management teams with issue analysis and resolution. Must have skills : Infor Lawson, Infor M3 Administration, Infor S3 Lawson Administration Good to have skills : NAMinimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :Manage Infor S3 and M3 customer application environments, Troubleshoot and resolve a...