Top Analysis Reporting Jobs
As a Cybersecurity Analyst, you will support various security testing and compliance projects, acting as a subject matter expert. Responsibilities include vulnerability management, penetration testing, incident response, and providing technical support. You will collaborate on documents, conduct training, and engage with the cybersecurity community.
The Senior Deal Desk Analyst at Komodo Health is responsible for managing deal operations, ensuring alignment with strategic goals, and optimizing deal structures. This role involves collaborating with sales, legal, and finance teams, establishing pricing strategies, and enhancing deal execution efficiency.
The Associate Director of Data Management will lead DM activities for clinical studies, ensuring high-quality data management deliverables. Responsibilities include overseeing data quality, project timelines, and vendor interactions while participating in cross-functional teams and supporting regulatory submissions.
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The Data Entry Specialist will manage data entry processes, ensuring accuracy and compliance with regulations. Responsibilities include filling out permit applications, entering data into systems, maintaining logs, troubleshooting issues, and assisting with administrative tasks while supporting data exception reviews and customer requirements.
The Senior Compliance & Privacy Analyst will assess systems for FedRAMP compliance, manage continuous monitoring activities, maintain documentation, and collaborate with engineering teams to ensure compliance is met. Key responsibilities include vulnerability assessments, assisting in authorization packages, and developing Compliance Framework artifacts.
As a Requirements Analyst, you will collaborate with cross-functional teams to clarify business requirements, document them, and communicate essential needs between stakeholders and IT services. Responsibilities include eliciting business requirements, creating user stories, managing requirement changes, and maintaining documentation in tools like Microsoft SharePoint and Salesforce. You will play a key role in ensuring accuracy in project goal alignment and quality assurance of documentation.
The Scientist will lead the development, characterization, and scale-up of RNA manufacturing processes. Responsibilities include designing experiments, authoring regulatory documents, and collaborating with partners for technology transfer and lot release assessments, while ensuring compliance with GMP guidelines.
The Systems Analyst II will enhance health plan quality measures by analyzing business requirements and translating them into technical solutions. Responsibilities include developing IT systems, improving business efficiency, collaborating with analysts, and working on data architecture and ETL flows for HEDIS data management.
As a Principal Scientist - DMPK, you will lead ADME/PK studies to support drug discovery, mentor a DMPK team, collaborate with medicinal chemists, and provide expertise in data analysis and experimental design. You will also manage DMPK activities, contribute to IND submissions, and troubleshoot issues with bioanalytical methods.
The Scientist II/Senior Scientist will oversee AAV purification processes, managing both internal and external CDMO operations. Responsibilities include optimizing large-scale purification techniques, mentoring junior staff, conducting process characterization, and ensuring compliance with regulatory standards. The role requires strategic thinking and problem-solving to enhance process development.
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