📑 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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📑 Job Description: Veeva QualityDocs and GxP Training System AdministratorJob Title: Veeva Veeva QualityDocs and GxP Training System Administrator AdministratorThe Veeva QualityDocs and GxP Training System Administrator is responsible for the management of Veeva QualityDocs and GxP Training.</ ...
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📑 Title: Technical Project Coordinator Duration : 6+ Months.Location: Parsippany, NJ.Rate: OpenRequirementsJob Description :Strong Master Data and Customer Relationship Data Management Solution Architect to collaborate with both Veeva and the Analyti ...
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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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📑 Job Details:Job Title: Interactive Visual Aid (IVA) SpecialistLocation: Mettawa, IL (Hybrid, Onsite 3 days/week) or RemoteDuration: 12 Months (With Possible Extension)Position Type: Full-Time, ContractPosition Overview:The Digital ...
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📑 Job SummaryWe are looking for a Veeva CRM Subject Matter Consultant for our Life Sciences client. This role is key in implementing and optimizing Veeva CRM solutions within the organization's Sales Force Operations. It requires a deep understanding of the Veeva CRM platform, its capabilities, and how it can be leveraged to meet ...
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📑 Job Description: The incumbent supports activities for Veeva electronic Document Management System (EDMS) based on Veeva Vault - QualitDocs. In the role, the incumbent is primarily responsible for supporting the Veeva Vault - Quality Suite platform which may include supporting platform enhancements updates, and/or end- ...
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📑 Job Details: 2-4 years experience with Veeva Vault Platform and Clinical Vault applications Good Understanding of clinical studies and operational datasets Working experience of Data and Content Migration<br / ...
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📑 Position Details: Our client, a world-leading Pharmaceutical Company in Jacksonville, FL is currently looking for a Veeva Vault Administrator to join their expanding team.Job Title: Veeva Vault Administrator / REMOTE WORK Duration: 9 months contract, extendable up to 24 mont ...
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📑 Why Patients Need You All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all c ...
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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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📑 Agile Methodology Good to have -Clinical domain, Oracle Apex knowledge, DevOps, New Billing/ Strategic/ Non- Exclusive 2024 - PDC Release 4.2.1 & 4.3 (Veeva)Senior PM, Good to have -Clinical domain, Oracle Apex knowledge, DevOps, Additional requirement : New Billing/ ...
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📑 Who We Are: At Neurocrine Biosciences, we pride ourselves on having a strong, inclusive, and positive culture based on our shared purpose and values. We know what it takes to be great, and we are as passionate about our people as we are about our purpose - to relieve suffering for people with great needs, but few optio ...
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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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📑 Role: Validation Engineer, RIMLocation: Remote A High School Diploma with 6+ years of relative experience OR an Associates Degree with 5+ years of relative experience OR A Bachelor's Degree with 4+ years of relevant experience or a Master's Degree (M.S./MBA)with 2+ years of relevant exp ...
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📑 Title: Vendor Quality SpecialistLocation: Fully RemoteContract: 6 months with possibility of conversion Support the GLP/GMP vendor management program, including maintaining the Approved Supplier List, performing vendor risk assessments, audit planning, scheduling, pre-audit meeting schedul ...
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📑 Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countrie ...
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📑 CONTENT MANAGEMENT-CONTENT CENTRAL LIBRARIANPrinceton Pike, NJPay Rate is $46.95 per hour. Top 3-5 skills:1. Scientific background, familiarity with different medical reference types, and medical terminology. Experience managing reference/core ...
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📑 Responsibilities: Business Analyst with IT GxP process and Business Process implementation experience. This person will need to be able to work in a very fast-paced and dynamic environment. Experience working in the Biotech/Pharma Industry. Develop and optimize test scripts usi ...
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📑 The Role We are looking for Front-end Software Engineers who are eager to build in a dynamic, startup environment inside a stable, profitable company. Our teams are solving complex problems that impact the speed and effectiveness of the life sciences industry. In this role, you’ll jump right in, develop in rapid sprints, and find qui ...
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📑 Job Title- PRC Coordinator Duration- 08/30/2024 3 months-up-to 6 months.Cambridge ,MAJob Summary:This role is a contract role (Short-term assignment)---the assignment could be as short as 3 months-up-to 6 months.Job Summary: The US Commerc ...
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📑 Hybrid 50%The U.S. Omnichannel Strategy team leads omnichannel planning, execution, and measurement in close partnership with Brand, Agency, Business Insights and Production teams. In this role, you will be responsible for the management and execution of omnichannel engagement plans to support a Client brand. You will serve as a dedicated p ...
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📑 Job Description: Provide Data and Business analysis support to the Enterprise Master Data Management organization focusing on Customer Master.Data Analysis Support for Ex-US Next Gen Customer Master: Works independently on large volume data sets, data analysis and comparison be ...
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📑 Hybrid 50% The U.S. Omnichannel Strategy team leads omnichannel planning, execution, and measurement in close partnership with Brand, Agency, Business Insights and Production teams. In this role, you will be responsible for the management and execution of omnichannel engagement plans to support a Client brand. You ...
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📑 Job description : We are looking for Senior Manager with experience in Digital analytics in pharma / life science, which includes the oversight of promotional activities, measure and optimize various marketing measures, HCP eligibility, targeting measurement and impact analysis of digital and MCM campaigns. </p ...
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📑 Job Overview: We are seeking a highly motivated and experienced Manager/Senior Manager to join our CMC Quality Control department. This role will oversee our external stability programs, supporting both commercial and clinical programs across all modalities and molecules. The successful candidate will work closely with internal QC repres ...
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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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📑 *This position is onsite in Ridgefield, CT & remote*Currently seeking a Global Case Management Associate (GCM) to join our Patient Safety & Pharmacovigilance (PSPV) team located at our Ridgefield, CT facility. The GCM will provide case processing and auditing support.Duties & Responsibilities:< ...
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📑 This role is a contract role (Short-term assignment)---the assignment could be as short as 3 months-up-to 6 months.Job Summary: The US Commercial Regulatory Affairs Promotional Review Committee (PRC) Coordinator is responsible for facilitating the promotional review committee process of assigned products for ...
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📑 Position: Content Central Librarian 58123-1Location: Lawrence Township NJ 08648Duration: 12 months (possibility of extension for the right candidate depending on performance)Pay rate: $47.96/ hour on W2 Top 3-5 skills:< ...
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📑 Data Entry SpecialistKelly Services is seeking a diligent and detail-oriented individual to join our team as an SFE & Trade Contractor as a Data Entry Specialist. In this role, you will collaborate directly with the Sales Forces Effectiveness (SFE) Team and the Ax Trade Team, focusing on operational support for our Ax ...
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📑 5+ years Validation specialist or engineer within Pharma or Biopharma Experience executing and writing test protocols Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ)Comprehensive knowledge of production processesKnowledge of Capa and Deviations Experience with Trackwise ...
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📑 Title: USA - Regulatory Affairs Ops Specialist I Location: Round Lake IL Hybrid - 3 days onsite, 2 remote Duration: 12 Months Pay Rate:$ 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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