554 Veeva Jobs - Page 10

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 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...

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...

About the job Our Team: Sanofi Business Operations (SBO) is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions. SBO strives to be a strategic and functional partner for tactical deliveries to Medical, HEVA, and Commercial organizations in Sanofi, Globally. Main responsibilities: The overall purpose and main responsibilities are listed below: Responsible for project management support and to ensure the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases. Initiate and amend su...

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...

Veeva CRM applications Azure Test Plans, JIRA, UAT, Testing Cycle, Charles, Debugger Fiddler or browser developer Testing Veeva CRM modules, CRM workflows and B2B integrations Salesforce CRM and cloud platforms Azure Selenium, Cucumber, Java, Groovy

About The Role About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire a...

About The Role About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire a...

About The Role About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire a...

About The Role About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Must have skills:R&D, Pharmacovigilance, regulatory Reporting Good to have skills:Core LS consulting Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire a...

About The Role About The Role Template Job Title - Life Sciences Commercial Analyst/ Consultant for S&C Global Network Management Level :Analyst/ Consultant Location:Bangalore/ Gurgaon/ Mumbai/ Hyderabad/ Pune/ Kolkata Must have skills: Must have experience working in one of the below-mentioned areas:Patient services | Multi-channel marketing and design | Customer relationship management (CRM) VEEVA/ Salesforce/ OCE | Medical Affairs Job Summary : As an Management consulting professional, you will support delivery of small to medium-size teams to deliver management consulting projects for global life science clients . Responsibilities may include strategy, implementation, process design and ...

About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functions such as Labo...

About The Role About The Role Job Title - Research & Development Consultant Life Sciences Management Level :09,11 Location:Bangalore/ Gurgaon/Hyderabad/Mumbai Job Summary : MBA from a Tier 1 institute or rich relevant industry experience 6+ years of progressive business and/or consulting experience; at least 1 year of experience in Life Sciences industry is mandatory Management consulting and general business consulting experience is a must Familiarity with assets OR tools in business consulting (R&D), such as issue trees, implementation frameworks, diagnosis tools like client questionnaire and analysis, operating model, business process mapping, and so on. Preferably worked with R&D functio...

About The Role About The Role Template Job Title - Life Sciences Commercial Analyst/ Consultant for S&C Global Network Management Level :Analyst/ Consultant Location:Bangalore/ Gurgaon/ Mumbai/ Hyderabad/ Pune/ Kolkata Must have skills: Must have experience working in one of the below-mentioned areas:Patient services | Multi-channel marketing and design | Customer relationship management (CRM) VEEVA/ Salesforce/ OCE | Medical Affairs Job Summary : As an Management consulting professional, you will support delivery of small to medium-size teams to deliver management consulting projects for global life science clients . Responsibilities may include strategy, implementation, process design and ...

Description Regulatory Consultant (CMC/ EU Market Exp) Syneos Healthis a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities Our Clinical Development model brings the customer and the patient to the center of everything that we do We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for Whether you join us in a Functional Service Provider partnership or a Full-Service environment, youll collaborate with passionate problem so...

About Amgen Amgen harnesses the best of biology and technology to fight the worlds toughest diseases, and make peoples lives easier, fuller and longer We discover, develop, manufacture and deliver innovative medicines to help millions of patients Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond whats known today About The Role The Digital Governance team supports the Global Regulatory Affairs and Strategy organization in the constant pursuit of Execution Excellence They do this by managing the tracking and documentation of Amgens global digital sites and projects for ...

Job Description: Amgen is a leading human therapeutics company in the biotechnology industry For more than 40 years, the company has tapped the power of scientific discovery and innovation to advance the practice of medicine As a Fortune 500 company serving millions of patients, Amgen continues to be an entrepreneurial, science-driven enterprise dedicated to helping people fight serious illness Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle...

About the job Project Specialists oversee and documents the creation and approval of documents required for events within their areas of responsibility within the OneCRM and PromoMat portal. They evaluate the type of event and organise the creation of the events information within the 1CRM portal that are within their scope, such as advisory board, consulting services, symposium, speaker training, scientific education program, stand-alone meeting, hospital-clinical staff meeting, third party sponsorships, etc. Project Specialists contribute their experience and knowledge in the form of recommendations to meet Sanofis purpose and goals, focusing on efficiency while always staying compliant at...

Our Team: Sanofi Business Operations (SBO) is designed to centralize processes and activities to support global medical business units and medical office. The Sanofi Business Operations is built to reduce reliance on external services providers and facilitate the development of internal expertise. The Sanofi Business Operations will leverage untapped combination of talent pool. Main responsibilities: The overall purpose and main responsibilities are listed below: Project Specialist will be responsible for processing contracts and related documents, connecting with stakeholders, and tracking ongoing work. Production (1) Support scientific events activities & external expert engagements (2) Pr...

Main responsibilities: Cross-Functional Collaboration: Act as a liaison between business partners, project sponsors, and project managers, ensuring alignment and accountability throughout the project lifecycle. Facilitate meetings with business partners, project managers, delivery leads providing direct updates on project status, production needs, and key next steps organized by country, indication or therapeutic area. Meeting Facilitation & Decision Documentation: Facilitate project meetings with content Operations/Omnichannel/GTMC teams, driving productive discussions, capturing key decisions, and updating action items accordingly. Project Assessment: Support business partners in assessing...

Main responsibilities: The overall purpose and main responsibilities are listed below: Project Specialist will be responsible for processing contracts and related documents, connecting with stakeholders, and tracking ongoing work. Production (1) Support scientific events activities & external expert engagements (2) Process contract and related documents within defined timelines (3) Check country specificities and handle queries received from country approver and/or external experts (4) Timely follow-ups with event leads, country approvers, and external experts Project Planning (1) Ensure delivery of ongoing projects as per agreed timelines (2) Ensure to follow defined/agreed quality paramete...