329 Inform Jobs - Page 5

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Sr Analyst Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 5 to 8 years 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 to life enabling them to improve outcomes by convergin...

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 Conduct thorough reviews of clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies and issues. Develop and maintain detailed reports of findings and recommendations for data improvements. Participate in developing and implementing process improvements to enhance data quality and efficiency. Provide training and support to junior staff members on data review procedures and best practices. Stay up-to-date with changing regulations and guidelines related to clinical data management. Job Requirements Strong understanding of clinical data manageme...

Roles and Responsibility Collaborate with cross-functional teams to develop and implement clinical trial protocols. Provide medical expertise and guidance on clinical research studies, including protocol development and review. Conduct site feasibility assessments and coordinate with investigators to ensure successful study execution. Develop and maintain relationships with key stakeholders, including sponsors, investigators, and regulatory agencies. Stay updated with changing regulations and guidelines governing clinical research, ensuring compliance and adherence to best practices. Participate in quality assurance activities to ensure high-quality deliverables. Job Requirements Strong unde...

Roles and Responsibility Manage and maintain accurate and up-to-date clinical trial data. Develop and implement effective data management plans and procedures. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Analyze and interpret complex data sets to inform business decisions. Develop and maintain reports and dashboards to track key performance indicators. Ensure data quality and integrity by implementing robust validation and verification processes. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with data analysis and interpretation tools and techniques. Excellent communication and collaboration s...

ZS Life Science R&D Technologist in Clinical development ZS life science R&D team partners with clients to discover and develop innovative medicines that improve patient's lives. Our work spans consulting, analytics and technology (services and platforms) projects across the several domains. We have 3500+ zs professionals that deliver R&D programs, $100MM+ invested in R&D data, analytics and technology assets and 100+ clients on R&D programs. Our Clinical/Drug Development division displays a substantial history of contributing to numerous client projects with significant results in drug development. The Drug Development R&D Technologists possess a deep understanding of technological solution...

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 GCP guidelines and regulatory requirements. Experience with data management systems, such...

Manage and resolve discrepancies in clinical trial data. Develop and implement effective data reconciliation processes. Collaborate with cross-functional teams to ensure accurate and timely resolution of data issues. Analyze and report on data trends and patterns to identify areas for improvement. Ensure compliance with regulatory requirements and industry standards. Provide training and support to junior team members on data reconciliation best practices. Job Requirements Strong understanding of clinical trial data management principles and practices. Experience with data reconciliation tools and technologies. Excellent analytical and problem-solving skills. Ability to work effectively in a...

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. Participate in code reviews and contribute to improving overall code quality. Stay up-to-date with industry trends and emerging technologies in Veeva EDC clinical programming. Job Requirements Strong understanding of Veeva EDC clinical programming principles and practices. Proficiency in developing complex programs using Veeva EDC tools and te...

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-solving skills and attent...

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, policies, and procedures. 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 effectively in a fast-paced enviro...

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Analyze large datasets to extract meaningful trends and patterns. Develop and maintain technical documentation of data systems and processes. Provide training and support to junior team members on R and SAS programming best practices. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with clinical trial data and statistical modeling techniques. Excellent analytical and problem-sol...

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 technical issues related to clinical data management. Job Requirements Strong knowledge of clinical data management principles and practices. Experience with Veeva EDC is highly desirable. Excellent ...

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 working with databases and querying languages like SQL. Excellent problem-solving skills and attenti...

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Conduct thorough data quality checks and ensure compliance with regulatory requirements. Provide expert-level support for data-related queries and issues. Stay up-to-date with industry trends and emerging technologies in clinical data analysis. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex statistical models. Excellent problem-solving skills and...

Conduct thorough reviews of clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies and issues. Develop and implement effective data management strategies to improve data quality and efficiency. Provide expert guidance on data interpretation, reporting, and visualization to stakeholders. Ensure timely completion of projects while maintaining high-quality standards. Participate in ongoing training and professional development to stay current with industry trends and best practices. Job Requirements Strong understanding of clinical trial design, protocols, and regulator...

Develop and maintain complex statistical models and databases using R and SAS programming languages. Analyze large datasets to identify trends and patterns, providing insights to stakeholders. Design and implement data visualizations to effectively communicate results. Collaborate with cross-functional teams to integrate data into business operations. Develop and maintain technical documentation of data systems and processes. Troubleshoot and resolve issues related to data quality and integrity. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and developing complex statistical models. Excellent analytical and problem-solving skil...

Conduct thorough reviews of clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies and issues. Develop and maintain detailed reports of findings and recommendations for data improvements. Participate in developing and implementing process improvements to enhance data quality and efficiency. Provide training and support to junior staff members on data review procedures and best practices. Stay up-to-date with changing regulations and guidelines related to clinical data management. Job Requirements Strong understanding of Good Clinical Practice (GCP) principles and reg...

Develop and maintain complex statistical models and databases for clinical trial data. Design and implement data visualization tools to effectively communicate insights to stakeholders. Collaborate with cross-functional teams to identify business needs and develop solutions. Conduct thorough data quality checks and ensure compliance with regulatory requirements. Provide expert-level support for data-related queries and issues. Stay up-to-date with industry trends and emerging technologies in clinical data analysis. Job Requirements Strong proficiency in R and SAS programming languages. Experience working with large datasets and complex statistical models. Excellent communication and problem-...

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-solving skills and attent...

Conduct thorough reviews of clinical trial data to ensure accuracy, completeness, and compliance with regulatory requirements. Collaborate with cross-functional teams to identify and resolve data discrepancies and issues. Develop and implement effective data management strategies to improve data quality and efficiency. Provide expert guidance on data interpretation and reporting to stakeholders. Stay up-to-date with changing regulations and guidelines related to clinical data management. Participate in ongoing training and professional development to enhance skills and knowledge. Job Requirements Strong understanding of clinical data management principles and practices. Proficient in using d...

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 Analyze and interpret complex clinical data to inform business decisions. Develop and maintain databases, spreadsheets, and reports using SAS and Veeva. Collaborate with cross-functional teams to design and implement data analysis solutions. Ensure data quality, integrity, and compliance with regulatory requirements. Provide technical support and training to junior team members on data analysis tools. Stay up-to-date with industry trends and emerging technologies in clinical data analysis. Job Requirements Strong proficiency in SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent pro...

Roles and Responsibility Manage and resolve discrepancies in clinical trial data. Collaborate with cross-functional teams to ensure accurate and timely data submission. Develop and implement effective data reconciliation processes. Analyze and report on data quality metrics to identify areas for improvement. Ensure compliance with regulatory requirements and industry standards. Provide training and support to junior team members on data reconciliation best practices. Job Requirements Strong understanding of clinical trial data management principles. Proficiency in data analysis and problem-solving skills. Excellent communication and interpersonal skills. Ability to work effectively in a fast...

Roles and Responsibility Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to ensure seamless integration of EDC systems. Develop and maintain technical documentation for EDC systems and applications. Troubleshoot and resolve issues related to EDC system performance and data quality. Provide training and support to end-users on EDC systems and applications. Participate in project planning, execution, and delivery to meet client requirements. Job Requirements Strong understanding of IT Service & Consulting principles and practices. Experience working with Veeva EDC clinical programming tools and technologies. Excellent...