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📑 Role: Veeva Solutions ArchitectLocation: Palo Alto, CA - Onsite RequiredDuration: Long-Term Rolling ContractROLE AND RESPONSIBILITIES:Manage & Maintain Veeva Vault Clinical operations (CTMS, eTMF) & Vault RIMAnalyze, develop, and implement Regulatory processes that solve business problems and support business needs using the Vault RIM suite (Submis ...

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📑 Role: Veeva Solutions Architect Location: Palo Alto, CA - Onsite Required Duration: Long-Term Rolling Contract ROLE AND RESPONSIBILITIES: Manage & Maintain Veeva Vault Clinical operations (CTMS, eTMF) & Vault RIM Analyze, develop, and implement R ...

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📑 Regulatory Clinical Trials Veeva Consultant Onsite at Tarrytown, NY 10591 Full Time OR 12 Months Contract It's a Banking Client. Main Skills: Veeva vault platform Gxp and non Gxp Key responsibilities: Experience working with Regulatory and Quality area in Clinical trials.< ...

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📑 Regulatory Clinical Trials Veeva Consultant Onsite at Tarrytown, NY 10591 Full Time OR 12 Months Contract It's a Banking Client. Main Skills: Veeva vault platform Gxp and non Gxp Key responsibilitie ...

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📑 IMMEDIATE CONTRACT NEED! (16 MONTH CONTRACT). OPEN TO REMOTE IN U.S. (EST HIGHLY PREFERRED).Looking for someone with hands on experience supporting and implementing Veeva Vault RIM Registrations platform is required. Veeva certification desiredIn this role, you will partner with Regulatory Affairs business areas to understand technology needs and e ...

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📑 IMMEDIATE CONTRACT NEED! (16 MONTH CONTRACT). OPEN TO REMOTE IN U.S. (EST HIGHLY PREFERRED).Looking for someone with hands on experience supporting and implementing Veeva Vault RIM Registrations platform is required. Veeva certification desiredIn this role, you will partner with Regulatory Affairs business areas to understand technology needs and ...

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📑 Global system experience working with Regulatory Affairs Strategy, Intelligence, Regulatory Information Mgt & Operations, and/or Submission Publishing domains in support of market authorization. Experience working with Clinical Operations team in the Quality space to manage Audits, Inspections, Vendor Oversight, and issues management such ...

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📑 Global system experience working with Regulatory Affairs Strategy, Intelligence, Regulatory Information Mgt & Operations, and/or Submission Publishing domains in support of market authorization. Experience working with Clinical Operations team in the Quality space to manage Audits, Inspections, Vendor Oversight, and ...

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📑 IMMEDIATE CONTRACT NEED! (16 MONTH CONTRACT). OPEN TO REMOTE IN U.S. (EST HIGHLY PREFERRED).Looking for someone with hands on experience supporting and implementing Veeva Vault RIM Registrations platform is required. Veeva certification desiredIn this role, you will partner with Regulatory Affairs business a ...

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📑 HCLTech is looking for a highly talented and self- motivated Veeva Global Program Director to join it in advancing the technological world through innovation and creativity.Job Title: Veeva - Global Program DirectorPosition Type: Full TimeLocation: Cary, NC – USAContact: Vaishali Tomar -vaishali.t@hcl.comRole/ResponsibilitiesBullet point list of sp ...

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📑 Our client, a leader in the pharmaceutical industry, is seeking a Regulatory Information Management Specialist to join their team. This role will be responsible for supporting data entry/management of regulatory information, data quality/stewardship, document management and RIM processes.**This job is remote - USA** **W2 Only**Responsibilities: Exe ...

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📑 This position will report to the Director of Regulatory Operations and will be responsible for maintaining the regulatory archives in the Veeva Vault system and the internal shared drive. The Manager/Senior Manager will be working with a diverse team of professionals providing support to various regulatory filings and projects.Responsibilities: ...

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📑 Our client, a leader in the pharmaceutical industry, is seeking a Regulatory Information Management Specialist to join their team. This role will be responsible for supporting data entry/management of regulatory information, data quality/stewardship, document management and RIM processes.**This job is remote - USA** **W2 Only**<b ...

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📑 Job DescriptionJob DescriptionRegulatory Information Management Specialist needed for a 100% remote, 12+ month contract with our client. JOB DESCRIPTIONResponsible for supporting data entry/management of regulatory information, data quality/stewardship, document management and RIM processes. The incumbent will have a general working knowledge of Re ...

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📑 Job Title/Role : Veeva Vault Technical Lead ContractRemote workMandatory SkillsVeeva Vault RIMSResource should have Veeva Vault admin training and certification. Should have experience on Veeva Registration , Submission , Clienthival , Quality Docs or other Veeva Vaults. Excellent Understandin ...

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📑 Job Title/Role : Veeva Vault Technical Lead ContractRemote workMandatory SkillsVeeva Vault RIMSResource should have Veeva Vault admin training and certification. Should have experience on Veeva Registration , Submission , Cl ...

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📑 Come join our team for an excellent role! We are looking for a Veeva Vault - Product Consultant!! We are seeking a Lead Product Consultant with a specialization in Vault QMS to join our team as a Sr. Manager - Projects. With a focus on enhancing our quality management systemsthe ideal candidate will bring a wealth of experience ...

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📑 Refer a friend: Career Developers Inc, a well-established staffing agency/consulting firm, is celebrating 30 years in business. Previously in Ramsey, NJ for 25 years and now headquartered in sunny West Palm Beach, FL, we offer comprehensive commercial and government staffing services nationwide (GSA Contract holder). With a port ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Responsibilities: Collaborate with project team members to architect solutions per Business Requirements. Perform analysis and design (functional/non-functional) activities to create clinical/Regulatory solution landscapes for our Life Sciences Clients. Take complex concepts and articulate them to an audience of varying level ...

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📑 Bonus + Equity + 401(k) + Benefits + REMOTEThis Jobot Job is hosted by: Katie GriffithAre you a fit? Easy Apply now by clicking the Apply buttonand sending us your resume.Salary: $180,000 - $220,000 per yearA bit about us:We are a rapidly growing therapeutics company with an approved drug on the market, leveraging scientific advances in B-cel ...

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📑 Responsibilities: Collaborate with project team members to architect solutions per Business Requirements. Perform analysis and design (functional/non-functional) activities to create clinical/Regulatory solution landscapes for our Life Sciences Clients. Take complex concepts and articulate them to an audience of var ...

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📑 BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Responsibilities: Collaborate with project team members to architect solutions per Business Requirements. Perform analysis and design (functional/non-functional) activities to create clinical/Regulatory solution landscapes for our Life Sciences Clients. Take complex concepts a ...

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📑 • Ensure day-to-day 2nd level support of incident management - queue management, timely resolution of incidents• Act as subject matter expert and technology expert for the Publishing tool, DocuBridge by Lorenz; assess release notes with the process owner; Upgrade the system; solve related issues.• Provide support to project ...

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📑 • Ensure day-to-day 2nd level support of incident management - queue management, timely resolution of incidents• Act as subject matter expert and technology expert for the Publishing tool, DocuBridge by Lorenz; assess release notes with the process owner; Upgrade the system; solve related issues.<b ...

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📑 Job Title: Regulatory Affairs Associate IDuration: 12 MonthsLocation: Round Lake, IL 60073 – HybridHybrid - 3 days onsite, 2 remote• Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission typeso Creating timelines for regulatory filingso Providing and maintain templates for authoring.o O ...

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📑 Kelly Science & Clinical is seeking a Regulatory Affairs Ops Specialist near Round Lake, IL.Long term contract = ~1 year contract Shift: Monday - Friday 1stHybrid - 3 days onsite, 2 remoteCompensation: based on experience Responsibilities:Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submi ...

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📑 Title: Regulatory Affairs Ops SpecialistDuration: 12 MonthsLocation: Round Lake, IL, 60073Hybrid - 3 days onsite, 2 remoteDescription:• Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission types• Creating timelines for regulatory filings• Providing and maintaining templates for authori ...

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📑 Hybrid - 3 days onsite, 2 remote Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission types o Creating timelines for regulatory filings o Providing and maintain templates for authoring. o Overseeing authoring and reviewing of regulatory documents o QC submiss ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 **General Description:**As part of BeiGenes Global Technology Solutions team, the Senior Business Analyst, will be responsible for implementation and management of BeiGenes Veeva application to meet regulatory requirements and business needs.The ideal candidate should bring experience working in enterprise application environments in life sciences ...

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📑 Title: Manager, Site ComplianceAbout the role: Step into a crucial role within a large medical device company as the Manager of Site Compliance. We are in search of an experienced leader to lead all site Quality regulatory compliance activities, play a pivotal role in maintaining the effectiveness of the ...

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📑 Hybrid - 3 days onsite, 2 remote Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submission types o Creating timelines for regulatory filings o Providing and maintain templates for authoring. o Overseeing authoring and reviewing of regulat ...

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📑 Title: USA - Regulatory Affairs Ops Specialist I Location: Round Lake IL Hybrid - 3 days onsite, 2 remote Duration: 12 Months Pay Rate:$ 28.00/hr on W2 to $ 32.00/hr on W2 Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, Clientrom, and other electronic submission types Creating ti ...

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📑 Roles and Responsibilities:Partner with Product teams, Client Technology Services and other architects to design scalable, flexible and supportable technical systems that drive business value for Client Global Regulatory AffairsDrive alignment to Enterprise and pharmaceutical R&D technology strategy, patterns and standardsDesign, maintain and socia ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead. At the heart of Veeva are our values: Do the Right T ...

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📑 Title: Regulatory Affairs Ops SpecialistDuration: 12 MonthsLocation: Round Lake, IL, 60073Hybrid - 3 days onsite, 2 remoteDescription:• Managing the preparation of regulatory submissions f ...

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📑 Job Title: Regulatory Affairs Associate IDuration: 12 MonthsLocation: Round Lake, IL 60073 – HybridHybrid - 3 days onsite, 2 remote• Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, AdProm, and other electronic submiss ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth potential ahead.At the heart of Veeva are our values: Do the Right Thing, ...

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📑 Job DescriptionJob DescriptionThis is a fully remote position.About fme...fme Life Sciences focuses on Business Solution deployments leveraging Enterprise Content Services platforms for clients in the Life Sciences Industry. fme is increasingly regarded as a trusted vendor and partner by its clients, who range from small and emerging start-ups to l ...

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📑 Kelly Science & Clinical is seeking a Regulatory Affairs Ops Specialist near Round Lake, IL.Long term contract = ~1 year contract Shift: Monday - Friday 1stHybrid - 3 days onsite, 2 remoteCompensation: based on experience ...

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📑 Title: USA - Regulatory Affairs Ops Specialist I Location: Round Lake IL Hybrid - 3 days onsite, 2 remote Duration: 12 Months Pay Rate:$ 28.00/hr on W2 to $ 32.00/hr on W2 Managing the preparation of regulatory submissions for IND, ANDA, NDA, 510K, Clientrom, and other ...

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📑 Responsibilities: Maintain Regulatory document management and tracking systemsCreate/archive Clinical Trial and Marketing Application submissions/Health Authority correspondenceResponsible for maintaining the on-site US Certificate of Pharmaceutical Product (CPP) responsibilities, as well ...

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