Sme Salary at Aegis Global Corp BETA

Job Description The Regulatory Compliance and Communication team is responsible for responding to a variety of information/data requests from Vegetation Management. For each request the team is responsible for determining the nature of the request, the most appropriate way to structure a response, and the appropriate SME to partner with to develop the report. We are looking for someone with the ability to manage & track the intakes and be able to evaluate the requests, analyze & research, and provide a synthesized response. We need someone comfortable working in a fast-paced environment who can handle a high volume of requests at one time. Required Skills & Experience - 2+ years of professional experience in a Business/Data Analyst, Project Coordinator, or Document specialist-type role - Some utility professional experience - Excellent stakeholder/SME communication - Ability to understand a request, perform appropriate research and coordination, and formulate a response Nice to Have Sk

The Regulatory Compliance and Communication team is responsible for responding to a variety of information/data requests from Vegetation Management. For each request the team is responsible for determining the nature of the request, the most appropriate way to structure a response, and the appropriate SME to partner with to develop the report. We are looking for someone with the ability to manage & track the intakes and be able to evaluate the requests, analyze & research and provide a synthesized response. We need someone who is comfortable working in a quick pace environment and can handle a high volume of request at one time. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (includin

Accenture Flex offers you the flexibility of local fixed-duration project-based work powered by Accenture, a leading global professional services company. Accenture is consistently recognized on FORTUNE's 100 Best Companies to Work For and Diversity Inc's Top 50 Companies For Diversity lists. As an Accenture Flex employee, you will apply your skills and experience to help drive business transformation for leading organizations and communities. In addition to delivering innovative solutions for Accenture's clients, you will work with a highly skilled, diverse network of people across Accenture businesses who are using the latest emerging technologies to address today's biggest business challenges. You will receive competitive rewards and access to benefits programs and world-class learning resources. Accenture Flex employees work in their local metro area onsite at the project, significantly reducing and/or eliminating the demands to travel. Key Responsibilities: + Install, Deploy, conf

About the job Presto SME/Platform Administrator ***W2 only*** Position: Presto SME/Platform Administrator Work Authorization: All Work Authorizations Location: 100% Remote (Must Work CENTRAL TIME HRS) Contract: 12+ months Requirements: Minimum of 2-3 years of Azure experience with 10+ years of IT experience Must have Unix and Windows background Must have strong experience with all Azure cloud components including Storage Accounts, Presto, Azure Kubernetes Service (AKS) at admin capacity. Must have clear understanding of NSGs, Azure baseline security guidelines. Azure certification (preferred) Experience with Azure Synapse (preferred) Experience with PowerBI (preferred) Proven ability to work with large cross functional teams with good communication skills Key Requirements: Experience with the following Azure cloud components at admin capacity: Storage Accounts Azure Kubernetes Service (AKS) Presto Detailed knowledge of Presto platform (more than an admin, looking for a SME) Scripting e

**At Bayer were visionaries, driven to solve the worlds toughest challenges and striving for a world where 'Health for all Hunger for none is no longer a dream, but a real possibility. Were doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining impossible. There are so many reasons to join us. If youre hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, theres only one choice.** **Senior Production Specialist Cell Suspension for Injection** The Senior Production Specialist Cell Suspension for Injection is a subject matter expert (SME) responsible for clinical manufacturing of novel cell therapy drug substance and drug product within the Cell Therapy Module, CT-MOD. In this role you will Collaborate closely with biological development(BD) and Manufacturing Science and Technology (MSAT) for new prod

Senior Director of Pharmacovigilance (PV) – Summary: Company Overview: Clinical-stage biopharmaceutical company focused on rare diseases. Located in the San Francisco Bay Area, CA. Key Responsibilities: Evaluate and assess adverse event (AE) reports for safety issues. Manage PV vendors and ensure compliance. Act as Subject Matter Expert (SME) for Individual Case Safety Report (ICSR) processing. Ensure AE reporting complies with global regulations (FDA, EMA, ICH). Update and create SOPs; lead process improvement initiatives. Collaborate with departments and partners on drug safety data exchange. Lead training on AE and product complaints for internal teams and vendors. Qualifications: Education: Bachelor’s in science/health-related field; advanced degrees are a plus. Experience: 10+ years in Pharmacovigilance, Drug Safety, or Risk Management. Knowledge: Strong understanding of global PV regulations (e.g., US CFR, EMA, ICH). Technical Skills: Proficiency with safety databases (e.g., Orac

Senior Director of Pharmacovigilance (PV) – Summary: Company Overview: Clinical-stage biopharmaceutical company focused on rare diseases. Located in the San Francisco Bay Area, CA. Key Responsibilities: Evaluate and assess adverse event (AE) reports for safety issues. Manage PV vendors and ensure compliance. Act as Subject Matter Expert (SME) for Individual Case Safety Report (ICSR) processing. Ensure AE reporting complies with global regulations (FDA, EMA, ICH). Update and create SOPs; lead process improvement initiatives. Collaborate with departments and partners on drug safety data exchange. Lead training on AE and product complaints for internal teams and vendors. Qualifications: Education: Bachelor’s in science/health-related field; advanced degrees are a plus. Experience: 10+ years in Pharmacovigilance, Drug Safety, or Risk Management. Knowledge: Strong understanding of global PV regulations (e.g., US CFR, EMA, ICH). Technical Skills: Proficiency with safety databases (e.g., Orac

Senior Director of Pharmacovigilance (PV) – Summary: Company Overview: Clinical-stage biopharmaceutical company focused on rare diseases. Located in the San Francisco Bay Area, CA. Key Responsibilities: Evaluate and assess adverse event (AE) reports for safety issues. Manage PV vendors and ensure compliance. Act as Subject Matter Expert (SME) for Individual Case Safety Report (ICSR) processing. Ensure AE reporting complies with global regulations (FDA, EMA, ICH). Update and create SOPs; lead process improvement initiatives. Collaborate with departments and partners on drug safety data exchange. Lead training on AE and product complaints for internal teams and vendors. Qualifications: Education: Bachelor’s in science/health-related field; advanced degrees are a plus. Experience: 10+ years in Pharmacovigilance, Drug Safety, or Risk Management. Knowledge: Strong understanding of global PV regulations (e.g., US CFR, EMA, ICH). Technical Skills: Proficiency with safety databases (e.g., Orac