Senior Regulatory Analyst - Princeton - beBeeBusinessAnalysis

You will drive project management and business analysis activities for Life Sciences projects. · Lead end-to-end project management and business analysis activities for Life Sciences initiatives. · Plan, manage, and execute projects to meet agreed-upon scope, timelines, budgets, ...

The Quality Assurance Analyst I will serve as a Quality Reviewer responsible for reviewing complaint records to ensure accuracy completeness and compliance within regulated medical device pharmaceutical environment. · Review assess complaint records for accuracy completeness comp ...

+Sr. PM with 10-15 years of experience in Pharmaceutical Industry especially in area of Regulatory Affairs. · +Dedicated technical and business savvy Project Manager with a good detailed project planning skills and ability to manage from a project plan. · Regulatory Affairs exper ...

We are looking for a Lead System Analyst – Generative AI / Agentic AI to drive the analysis, design, and delivery of enterprise-grade AI solutions powered by LLMs and autonomous agents. · This role provides technical and functional leadership ensuring that GenAI and agentic syste ...

This role will involve reviewing and assessing complaint records for accuracy and compliance with regulatory requirements. The successful candidate will provide clear feedback to complaint owners and investigators. · ...

This position involves reviewing complaint records in accordance with internal procedures and regulatory requirements. · ...

This role manages global communications, system approvals, and user support for VEEVA VAULT PromoMats and related platforms.It ensures smooth operations across multiple systems, supports global user adoption, and partners with cross-functional teams to maintain compliance and eff ...

This role manages global communications, system approvals, and user support for Veeva Vault PromoMats and related platforms. · ...

Dice is seeking Quality Assurance Analyst for SGS Consulting in Princeton. · ...

The Quality Assurance Analyst I will serve as a Quality Reviewer, · responsible for reviewing and approving complaint records to ensure accuracy, · completeness, and compliance with internal procedures and applicable regulatory requirements. · This role supports complaint handlin ...

Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds... · ...

The incumbent position will work with a lead BA/PM in specific R&D areas to analyze processes, design processes, · defined/document high level business requirements and perform data analysis that will lead to finalization of strategy.. · Analyzing systems and process integration ...

Review and assess complaint records for accuracy and compliance with internal procedures. · ...

Project Manager/BA with experience in pharmaceutical company/CRO and business analyst along with project management. Strong understanding/knowledge on clinical research and development area with regulatory documentation and end to end clinical business and technical process. · 9- ...

We are seeking an experienced Compliance Lead to manage our audit readiness efforts in Princeton NJ or Rockville MD offices. · Lead efforts with regard to Audit readiness Periodic Reviews managing CAPA/Deviation goals & objectives. · Collaborate closely with Internal External Aud ...

The Junior Business Analyst – Salesforce will support the analysis, design, and delivery of Salesforce solutions with a focus on Health Cloud or Veeva CRM. · Elicit analyze and document business requirements from stakeholders Translate business requirements into detailed technica ...

+Job summary:The primary responsibilities of an Associate Director Medical Writer at client include, but are not limited to, leading key medical writing projects and activities across therapeutic areas and preparing (under minimal supervision) scientific and regulatory documents ...

+The company is looking for a Medical Writer III to work on medical writing projects and activities across therapeutic areas. The primary responsibilities include leading key medical writing projects and preparing scientific and regulatory documents related to the clinical develo ...

This role manages global communications, system approvals and user support for Veeva Vault PromoMats and related platforms. It ensures smooth operations across multiple systems supports global user adoption partners with cross-functional teams to maintain compliance efficiency in ...

This role manages global communications, system approvals and user support for Veeva Vault PromoMats and related platforms ensuring smooth operations across multiple systems supports global user adoption partners with cross-functional teams to maintain compliance efficiency in pr ...

+The Digital Marketing Specialist is a critical matrix team partner for the Brand and Omnichannel Planning teams. · ...