SAS EG Jobs

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SAS EG

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🔥 Bank Credit Risk Analyst Senior - Retail Banking

Posted about 3 hours ago

📍 United States

🧭 Full-Time

💸 120550.0 - 230400.0 USD per year

🔍 Retail Banking

🏢 Company: USAAJOBSWD

🔧 Requirements

6 years of experience in an analytical field or work focused on leading analytical projects, advanced analytics, risk assessments or bank credit risk data
Experience in financial analysis activities to support risk strategy.
Strong understanding of banking regulations, risk, and/or compliance.
Advanced presentation and communication skills.
Advanced knowledge of Microsoft Office products, particularly Excel, Word, and PowerPoint.
Advanced knowledge of data analysis tools including skills to develop analysis queries and procedures in SQL, SAS, or other business intelligence and analysis software applications for data segmentation, aggregation, and statistics (E.g., SPS or Visual Basic).
Knowledge of federal laws, rules, regulations, and applicable guidance to include: FCRA, Reg B, UDAAP/UDAP, OCC Heightened Standards, OCC CREDIT RISK GUIDANCE.

💡 Responsibilities

Applies industry leading practices and analytical skills to identify risks and opportunities within the handled portfolio and translates results into strategic solutions with the delivery of credit risk strategies.
Applies critical thinking skills to synthesize analyses, identify root causes, and develop clear and concise recommendations to drive credit risk strategy development and influence senior decision makers.
Partners to deliver Bank credit risk strategies across lines of defense by effectively developing and improving complex analytical frameworks, analyzing data and processes, and clearly communicating insights/recommendations to key partners and leadership.
Analyzes internal and external scores/data for use in identifying first party fraud.
Applies industry knowledge and driven benchmarking to advise credit strategy development.
Uses advanced and nuanced quantitative analysis based upon internal and external data sources to bring structure and clarity to ambiguous and exciting problems.
Develops, handles, and presents comprehensive risk and financial reporting in support of senior management and committee oversight of existing and emerging risks and escalates the quality and direction of credit performance to appropriate levels of management.
Designs and performs complex financial risk sensitivity analysis.
Builds and handles credit strategy infrastructure and ensures credit strategies are implemented as intended.
Applies expert programming and analytical techniques to analyze credit data.
Provides thought leadership, coaching, and mentoring to team members regarding analytics and risk management.
Collaborates with key partners to guide & facilitate teams in the development and implementation of key initiatives.
Applies analytically derived insights to develop strategic plans with significant impact to business results.
Coaches and mentors other analysts and acts as a leader with vision within the analyst community.
Ensures risks associated with business activities are optimally identified, measured, monitored, and controlled in accordance with risk and compliance policies and procedures.

Python SQL Data Analysis SAS EG Algorithms Data Structures REST API Regression testing Communication Skills Analytical Skills Microsoft Excel Problem Solving Attention to detail Presentation skills Written communication Compliance Reporting Risk Management Data visualization Financial analysis Analytical thinking Data modeling Data analytics Data management

Posted about 3 hours ago

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🔥 PL Product Management Assistant

Posted 1 day ago

📍 Argentina

🔍 Insurance

🏢 Company: Capgemini👥 10001-350000 IT Services and IT Consulting

🔧 Requirements

Experience in this field: Minimum: 1-3 years, Preferred: 4-6 years
Experience in Insurance Companies: Required (Personal Lines is preferred, but background in commercial or business lines is also accepted)
Bachelor's degree in related fields
Strong Microsoft Office skills, including Excel and Access
Basic programming skills for statistical purposes, preferably in SAS
Excellent verbal and written communication skills including ability to make effective presentations
Demonstrated ability to secure 'buy-in' and convince others regarding best approach
Goal oriented team player with a positive attitude
Excellent time management skills
Strong relationship building
Fluency in English

💡 Responsibilities

Analyze information using data correlation, and statistical analysis. Develop data and information structure.
Create and modify computer programs to extract information from company databases.
Prepare state indications and other analyses of loss experience, retention, and expense data.
Suggest enhancements to standard methodologies.
Perform primary field research, including customer, distribution, competitor, insurance department, and market surveys.
Work with State Offices to support rate proposal and marketing plan development.
Identify market segments and develop specialized pricing approaches.
Prepare exhibits for state filings and respond to requests from regulators for additional data.
Provide detailed requirements for systems implementation projects.
Measure and monitor performance of states, initiatives, and identified segments.

SQL Agile Data Analysis Microsoft Access Microsoft SQL Server Product Management SAS EG Analytical Skills Microsoft Excel Microsoft Office Presentation skills Time Management Written communication Verbal communication Data visualization Financial analysis Data modeling English communication

Posted 1 day ago

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🔥 Sr. Director, Clinical Pharmacologist

Posted 10 days ago

📍 US

🧭 Full-Time

🔍 Pharmaceuticals

🏢 Company: Centessa Pharmaceuticals, LLC

🔧 Requirements

PhD or equivalent in pharmacokinetics (PK)/pharmacodynamics (PD), pharmacology, pharmaceutical sciences, or a closely related discipline.
Minimum 5 years of pharmaceutical industry experience in clinical pharmacology overseeing development of small drug molecules (focus) and large molecules.
Strong experience of scientific and operational leadership of clinical pharmacology strategies/studies to support clinical development and regulatory submissions (CNS preferred). Deep understanding and experience in the utility of how model-informed drug development in CNS drug development is a plus.
Experience in authoring clinical study protocols, reports and regulatory documents such as INDs; experience in NDAs is also preferred.
Hands on experience conducting standard non-compartmental and compartmental PK analysis, PK/PD analyses for drug development projects to support decision making, dose selection and dosing regimen optimization and regulatory interactions. Advanced proficiency in using clinical pharmacology software tools including, but not limited to NONMEM, r, Phoenix, NMLE, and/or SAS preferred.
Knowledge of study protocols, clinical endpoints and PK/PD modeling for sleep disorders is highly desirable.
Working knowledge of US and EU regulatory requirements and guidelines.
Be able to work in a matrix team environment and influence the team with a data-driven approach.
Good interpersonal and communication skills with the ability to articulate complex ideas/findings to internal stakeholders to ensure clarity and understanding.

💡 Responsibilities

Lead clinical pharmacology activities for the assigned projects and accountable for the planning ad exaction of clinical pharmacology strategies.
Plan and direct clinical pharmacology studies in collaboration with internal and external partners, including collaboration with KOLs in neurology and sleep research.
Use PK/PD modeling and translational clinical outcome measures to support dose selection, efficacy, and safety assessment of drug candidates.
Oversee clinical pharmacology vendors and ensure accurate and efficient PK data collection.
Apply pharmacokinetic and pharmacodynamic modeling and simulation techniques to optimize study design, data analysis, and interpretation.
Advise and draft the relevant sections of the clinical study protocols, reports, and regulatory documents in compliance with relevant guidelines and standards.
Communicate and present clinical pharmacology findings and recommendations to internal and external stakeholders.
Interface cross-sectionally across all disciplines involved in drug development including nonclinical pharmacology/toxicology, ADME, clinical, regulatory, and CMC.
Maintain flexibility in working through virtual and in-person interactions to coordinate with global team members and vendors.
Author scientific publications and present at scientific conferences.
Provide effective vendor overnights to ensure high quality data delivery

Leadership Data Analysis SAS EG Communication Skills MS Office Data visualization

Posted 10 days ago

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🔥 Senior Clinical Data Manager

Posted 22 days ago

📍 UK, Spain, Poland, Slovakia, Romania, Hungary, Serbia

🧭 Full-Time

🔍 Data Management

🏢 Company: Precision for Medicine

🔧 Requirements

8+ years’ experience with strong Oncology and/or Orphan Drug therapeutic experience
Experience in a clinical, scientific or healthcare discipline
Dictionary medical coding (MedDRA and WHODrug)
Experience in utilizing various clinical database management systems
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook

💡 Responsibilities

Manage all aspects of the clinical trial data management process from study start up to post database lock for assigned projects
Oversee and/or perform database development and testing
Act as Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s)

Project Management SQL Data Analysis Data Mining ETL SAS EG Reporting Data entry Data visualization Stakeholder management Data modeling Data analytics Data management

Posted 22 days ago

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🔥 Senior Clinical Data Manager

Posted 22 days ago

📍 UK, Spain, Poland, Slovakia, Romania, Hungary, Serbia

🧭 Full-Time

🔍 Data Management

🏢 Company: Precision Medicine Group👥 1001-5000💰 $35,160,000 almost 4 years agoPharmaceutical Biotechnology Medical Precision Medicine Health Care

🔧 Requirements

8+ years’ experience with strong Oncology and/or Orphan Drug therapeutic experience
Experience in a clinical, scientific or healthcare discipline
Dictionary medical coding (MedDRA and WHODrug)
Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.…)
Experience in utilizing various clinical database management systems
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Professional use of the English language; both written and oral

💡 Responsibilities

Primary Data Management (DM) contact for assigned clinical project(s)
Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing
Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
Conduct database build UAT and maintain quality controlled database build documentation
Specify requirements for all edit check types
Responsible for creating, revising, appropriate versioning and maintaining data management documentation
Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed
Review and query clinical trial data according to the Data Management Plan
Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM
Run patient and study level status and metric reporting
Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency
Coordinate SAE/AE reconciliation
Liaises with third-party vendors such as external data and EDC vendors in a project manager capacity in support of timelines and data-related deliverables
May assist with SAS programming and quality control of SAS programs used in the Data Management department
Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders
May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project
Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
May attend strategy meetings, bid defense prep meetings, bid defenses, capability presentations, potential client engagement meetings
May review Request for Proposals (RFP), proposals, provide project estimates
Provide leadership for cross-functional and organization-wide initiatives, where applicable
Trains and ensures that all data management project team members have been sufficiently trained
Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues
May present software demonstrations/trainings, department/company training sessions, present at project meetings
Perform other duties as assigned

SQL ETL SAS EG Data entry Data modeling Data analytics Data management

Posted 22 days ago

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🔥 Senior Clinical Data Manager/Principal Clinical Data Manager

Posted about 1 month ago

📍 United States

🧭 Full-Time

💸 113000.0 - 152800.0 USD per year

🔍 Clinical Research

🏢 Company: Precision Medicine Group👥 1001-5000💰 $35,160,000 almost 4 years agoPharmaceutical Biotechnology Medical Precision Medicine Health Care

🔧 Requirements

8+ years’ experience for a Sr. Clinical Data Manager and 10+ years for a Principal Clinical Data Manager
Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook
Able to handle a variety of clinical research tasks
Excellent organizational and communication skills
Professional use of the English language; both written and oral
Experience in utilizing various clinical database management systems
Broad knowledge of drug, device and/or biologic development and effective data management practices
Strong representational skills, ability to communicate effectively orally and in writing
Strong leadership and interpersonal skills
Ability to undertake occasional travel

💡 Responsibilities

Manage all aspects of the clinical trial data management process from study start up to post database lock for assigned projects
Oversee and/or perform database development and testing
Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s)
Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing
Provide input, assesses and manage timelines
Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
Conduct database build UAT and maintain quality controlled database build documentation
May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc.
Responsible for creating, revising, appropriate versioning and maintaining data management documentation
Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed
Review and query clinical trial data according to the Data Management Plan
Perform line listing data review based on the guidance provided by the sponsor and/or Lead DM
Run patient and study level status and metric reporting
Perform medical coding of medical terms
Coordinate SAE/AE reconciliation
Liaises with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables
Identify and troubleshoot operational problems, issues, obstacles, and barriers for studies
Participate in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities
Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues

Leadership Project Management SQL Data Analysis Data Mining SAS EG Project Coordination Communication Skills Microsoft Office Agile methodologies Written communication Data entry Data visualization Data modeling Data analytics Data management

Posted about 1 month ago

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🔥 Biostatistics Senior Manager, Rare Disease

Posted 4 months ago

📍 United States of America

💸 157846.0 - 184097.0 USD per year

🔍 Clinical

🏢 Company: careers

🔧 Requirements

Doctorate degree and 2 years of industry experience OR Master’s degree and 4 years of industry experience OR Bachelor’s degree and 6 years of industry experience OR Associate’s degree and 10 years of industry experience OR High school diploma / GED and 12 years of industry experience
Life Cycle Drug Development Experience (Pre-clinical Development, Clinical Development, and Post-marketing)
Experience in Inflammation therapeutic area clinical development
Strong verbal and written communication combined with organizational skills and cross-cultural sensitivity
Statistical leadership and contribution to regulatory and reimbursement submissions. of regulatory guidelines.
Experience working effectively in a globally dispersed team environment with cross-cultural partners.

💡 Responsibilities

Support biostatistical activities for Clinical Development, Clinical Operations, Medical Affairs, and Business Development
Provide statistical expertise and leadership to ensure program objectives are in alignment with regulatory and commercial needs
Serve as primary author for statistical sections of protocol
Create accompanying statistical documents (e.g., statistical analysis plan and mocked shells)
Participate in development of EDC database and interactive response technology (IxRS) specifications
Collaborate with project management, regulatory, medical affairs, PV/safety, business development, and commercial functions
Implement innovative statistical techniques that will provide benefit to clinical development programs
Contribute to strategic planning and go/no go decision guidance
Review biostatistics and statistical programming tasks outsourced to vendors
Perform statistical analyses and create statistical text for clinical publications and other communications, perform SAS programming validation if needed
Support the preparation of regulatory submissions documents including summaries of clinical safety and efficacy of BLA/NDAs if needed
Ensure timeliness and quality of deliverables
Travel as needed to execute assigned responsibilities.

SQL Data Analysis SAS EG Data visualization

Posted 4 months ago

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🔥 Lead/Principal Statistical Programmer Consultant(Hematology, Clinical Trials) REMOTE@CANADA

Posted 4 months ago

📍 Canada

🧭 Contract

🔍 Clinical Trials, Hematology

🏢 Company: ClinChoice

🔧 Requirements

Bachelor’s degree in computer science, statistics, or related scientific disciplines with 8 years of clinical programming experience.
Master’s degree in CS, statistics, or related disciplines with 7 years of clinical programming experience.
Oncology/Hematology therapeutic area experience required.
ISS & ISE experience is required.
Working knowledge of ICH and Good Clinical Practices.
Strong communication and coordination skills.

💡 Responsibilities

Lead and support all programming activities per project strategies.
Develop Tables, Figures, Listings (TFLs) deliverables from SAS programs.
Customize outputs and graphics based on delivery specifications.
Support the programming deliveries of clinical studies.
Communicate and escalate risks associated with assigned studies.

Leadership Data Analysis SAS EG Communication Skills Analytical Skills Microsoft Excel

Posted 4 months ago

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🔥 Junior Research Associate, JRA

Posted 6 months ago

📍 Philippines, Mexico

🧭 Full-Time

🔍 Market Research

🏢 Company: Hireframe👥 101-250 Management Consulting Consulting Sales Professional Services

🔧 Requirements

Some prior market research experience, preferably with a research vendor company
Knowledge of research techniques through coursework, internships, or work experience
Familiarity with market research tools and statistical software (such as SPSS, SAS, Qualtrics, and/or Alchemer)
Proficiency in Excel, PowerPoint, and Outlook
Strong attention to detail, ability to prioritize tasks, and contribute to multiple projects simultaneously
Capable of working independently and within teams
Excellent interpersonal, problem-solving, and project management skills
Excellent verbal and written communication skills

💡 Responsibilities

Perform tasks and responsibilities required with thoroughness to produce high-quality, high-accuracy market research deliverables.
Load, test, and proofread all research surveys and content on staging before posting live to production.
Assure data accuracy and relevance to objectives at every step in the project process to ensure the data is both internally consistent and demonstrates face validity.
Design and program research instruments (utilizing multiple methodologies, both qualitative and quantitative within the community) to answer research and business questions.
Prioritize tasks, communicate effectively, and remain flexible to meet client needs.
Ensure all project components are executed within the scope contract and/or project proposal, and all timelines for met.
Assist with daily moderation of research activities in the communities and extract insights. Oversee data collection and ensure quotas are met and data quality is achieved.

Leadership Project Management Data Analysis SAS EG Project Coordination Cross-functional Team Leadership Communication Skills Analytical Skills Collaboration Microsoft Excel PowerPoint

Posted 6 months ago

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