552 Veeva Jobs - Page 2

About The Role Project Role : Quality Engineer (Tester) Project Role Description : Enables full stack solutions through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Performs continuous testing for security, API, and regression suite. Creates automation strategy, automated scripts and supports data and environment configuration. Participates in code reviews, monitors, and reports defects to support continuous improvement activities for the end-to-end testing process. Must have skills : Oracle Argus Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years fu...

About The Role Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Veeva Vault Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Veeva Application Development SME, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure ...

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Veeva Vault Good to have skills : NA Minimum 3 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Veeva Vault Safety Application Senior Developer, you will be responsible for designing, building, and configuring applications to meet business process and application requirements using Veeva Vault modules. Your typical day will involve collaborating with cross-functional teams, analyzing business requirements, and developing solutions to meet those ...

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 functi...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : Veeva Vault Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Veeva Vault Safety Application Support Lead, you handling incoming incidents, tickets, change requests and problem tickets. Your typical day will involve collaborating with cross-functional teams, analyzing business requirements, and developing solutions to meet those requirements for change management and handling the team. It is expected that you wi...

About The Role Project Role : Quality Engineering Lead (Test Lead) Project Role Description : Leads a team of quality engineers through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Applies business and functional knowledge to develop end-to-end testing strategies through the use of quality processes and methodologies. Applies testing methodologies, principles and processes to define and implement key metrics to manage and assess the testing process including test execution and defect resolution. Must have skills : Functional Test Planning Good to have skills : NA Minimum 5 year(s) of experience is requir...

About The Role Project Role : Quality Engineering Lead (Test Lead) Project Role Description : Leads a team of quality engineers through multi-disciplinary team planning and ecosystem integration to accelerate delivery and drive quality across the application lifecycle. Applies business and functional knowledge to develop end-to-end testing strategies through the use of quality processes and methodologies. Applies testing methodologies, principles and processes to define and implement key metrics to manage and assess the testing process including test execution and defect resolution. Must have skills : Functional Test Planning Good to have skills : NA Minimum 3 year(s) of experience is requir...

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 ...

Develop and maintain databases, spreadsheets, and reports for tracking and analyzing clinical trial data.Collaborate with cross-functional teams to ensure accurate and timely delivery of high-quality results. Required Candidate profile Strong knowledge of SAS programming language and its applications in clinical trial data analysis. Experience with Veeva or similar systems is desirable.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong proficiency in SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Collaborate with cross-functional teams to ensure accurate and timely delivery of clinical data. Required Candidate profile Strong knowledge of Veeva EDC system and its applications in clinical trials. Experience in managing clinical data in a fast-paced environment. Excellent analytical and problem-solving

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Ensure compliance with regulatory requirements and industry standards for clinical data management Required Candidate profile Strong knowledge of Veeva EDC and clinical data management principles. Excellent analytical and problem-solving skills with attention to detail. Ability to work effectively in a team environment

Develop high-quality regulatory documents, including clinical trial applications and marketing authorizations.Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Required Candidate profile Minimum 2 years of experience in regulatory medical writing or a related field. Strong knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines.

Manage and oversee the development, implementation, and maintenance of clinical data management systems.Collaborate with cross-functional teams to ensure accurate and timely delivery of clinical data Required Candidate profile Strong knowledge of Veeva EDC system and its applications in clinical data management. Excellent analytical and problem-solving skills with attention to detail.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams to design Required Candidate profile Strong knowledge of SAS programming language and Veeva software. Experience working with large datasets and performing complex data analysis tasks. Excellent problem-solving skills

Role & responsibilities Reviews the asset files shared by the project owner. Performs thorough analysis of the content for completeness and accuracy and communicates with stakeholders. Performs coding as per the requirement shared. Enables interactivity on the target platform (VEEVA) Controls versioning of deliverables. Implements business rules for presentations in Veeva. Uploads content as per Veeva requirements. Performs peer review for unit and integration checks. Participates issue resolution and defect fixing. Understand and follow the End-to-End process of all digital content deliverables. Identifying redundant tasks and pushing for better ways of working. Ensure adherence to latest/r...

Manage and oversee the development, implementation, and maintenance of clinical data management systems. Ensure compliance with regulatory requirements and industry standards for clinical data management. Required Candidate profile Strong knowledge of Veeva EDC and clinical data management principles. Excellent analytical and problem-solving skills with attention to detail.

Analyze and interpret complex clinical trial data to inform business decisions.Develop and maintain databases, spreadsheets, and reports using SAS and Veeva.Collaborate with cross-functional teams Required Candidate profile Strong understanding of clinical trial design, protocols, and statistical analysis plans. Proficiency in programming languages such as SAS and Veeva. Experience with data management systems

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 Required Candidate profile Strong knowledge of Veeva EDC clinical programming principles and practices. Experience with EDC system implementation and maintenance. Excellent problem-solving skills and attention to detail.

Analyze and interpret complex clinical trial data using SAS. Develop and maintain databases, data systems, and computer models for clinical trial management. Collaborate with cross-functional teams. Required Candidate profile Strong proficiency in SAS programming language. Experience with Veeva or similar clinical trial management systems. Excellent analytical, problem-solving, and communication skills.

Manage and oversee the development, implementation, and maintenance of clinical data management systems. Collaborate with cross-functional teams to ensure accurate and timely delivery of clinical data. Required Candidate profile Strong knowledge of Veeva EDC system and its applications in clinical trials. Experience in managing clinical data from various sources, including electronic health records and laboratory results.

Design, develop, and implement Veeva EDC clinical programming solutions for clients. Collaborate with cross-functional teams to ensure seamless integration of Veeva EDC ystems. Required Candidate profile Strong understanding of Veeva EDC principles and technologies. Experience with clinical trial data management systems. Excellent problem-solving skills and attention to detail.

This is an exciting role and would entail you to • Oversee the end-to-end submission process of materials to the MLR review platform (Veeva Vault Promo Mats) • Understand and document client-mandated submission requirements and ensure these protocols are maintained with guidance from MLR/Submission managers • Create, uphold, and maintain submission checklists for assigned brands and ensure accurate and timely MLR submissions into Client systems • Maintain a comprehensive and accurate record of all current and upcoming submissions including the stage of review, job codes, references, and deadlines • Annotate any notes/comments relevant to MLR reviewers onto the submission file (As required, f...

As a Deputy Manager Regulatory Affairs at PolyPeptide Group, you will play a crucial role in bridging operational execution with strategic oversight, ensuring compliance with global regulatory requirements and contributing to the success of the company. **Key Responsibilities:** - **Drug Master File (DMF) Management** - Prepare, review, and submit DMFs in compliance with US (FDA), EU (ASMF and CEP), Canada, China, Korea, Brazil, and other emerging market regulations. - Maintain and update DMFs throughout their lifecycle, including change filings and regulatory correspondence. - **Regulatory Strategy & Compliance** - Develop and implement regulatory strategies for generic synthetic, semi-synt...

Description Associate RA ( Module 1, regulatory submission) 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 pro...