SAS EG Job Salaries

Find salary information for remote positions requiring SAS EG skills. Make data-driven decisions about your career path.

SAS EG

Median high-range salary for jobs requiring SAS EG:

$168,448.5

This analysis is based on salary ranges collected from 2 job descriptions that match the search and allow working remotely. Choose a country to narrow down the search and view statistics exclusively for remote jobs available in that location.

The Median Salary Range is $135,423 - $168,448.5

25% of job descriptions advertised a maximum salary above $184,097.

Skills and Salary

Specific skills can have a substantial impact on salary ranges for jobs that align with these search preferences. Certain in-demand skills are highly valued by employers and can significantly boost compensation. These skills often reflect the unique requirements and challenges faced by professionals in these roles. Some of the most sought-after skills that correlate with higher salaries include SQL, Data Analysis and Data visualization. Mastering these skills can demonstrate expertise and make individuals more competitive in the job market. Employers often prioritize candidates who possess these skills, as they can contribute directly to the organization's success. The ability to effectively utilize these skills can lead to increased earning potential and career advancement opportunities.

SQL
100% jobs mention SQL as a required skill. The Median Salary Range for these jobs is $135,423 - $168,448.5
- 25% of job descriptions advertised a maximum salary above $184,097.
Data Analysis
100% jobs mention Data Analysis as a required skill. The Median Salary Range for these jobs is $135,423 - $168,448.5
- 25% of job descriptions advertised a maximum salary above $184,097.
Data visualization
100% jobs mention Data visualization as a required skill. The Median Salary Range for these jobs is $135,423 - $168,448.5
- 25% of job descriptions advertised a maximum salary above $184,097.
Leadership
50% jobs mention Leadership as a required skill. The Median Salary Range for these jobs is $113,000 - $152,800
Project Management
50% jobs mention Project Management as a required skill. The Median Salary Range for these jobs is $113,000 - $152,800
Data Mining
50% jobs mention Data Mining as a required skill. The Median Salary Range for these jobs is $113,000 - $152,800
Project Coordination
50% jobs mention Project Coordination as a required skill. The Median Salary Range for these jobs is $113,000 - $152,800
Communication Skills
50% jobs mention Communication Skills as a required skill. The Median Salary Range for these jobs is $113,000 - $152,800
Microsoft Office
50% jobs mention Microsoft Office as a required skill. The Median Salary Range for these jobs is $113,000 - $152,800

Industries and Salary

Industry plays a crucial role in determining salary ranges for jobs that align with these search preferences. Certain industries offer significantly higher compensation packages compared to others. Factors such as industry size, profitability, and market trends can influence salary levels within these sectors. It's important to consider industry-specific factors when evaluating potential career paths and salary expectations.

Clinical
50% jobs are in Clinical industry. The Median Salary Range for these jobs is $157,846 - $184,097

Disclaimer: This analysis is based on salary ranges advertised in job descriptions found on Remoote.app. While it provides valuable insights into potential compensation, it's important to understand that advertised salary ranges may not always reflect the actual salaries paid to employees. Furthermore, not all companies disclose salary ranges, which can impact the accuracy of this analysis. Several factors can influence the final compensation package, including:

Negotiation: Salary ranges often serve as a starting point for negotiation. Your experience, skills, and qualifications can influence the final offer you receive.
Benefits: Salaries are just one component of total compensation. Some companies may offer competitive benefits packages that include health insurance, paid time off, retirement plans, and other perks. The value of these benefits can significantly affect your overall compensation.
Cost of Living: The cost of living in a particular location can impact salary expectations. Some areas may require higher salaries to maintain a similar standard of living compared to others.

Jobs

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🔥 Senior Clinical Data Manager/Principal Clinical Data Manager

Posted 29 days ago

📍 United States

🧭 Full-Time

💸 113000.0 - 152800.0 USD per year

🏢 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

Primary Data Management (DM) contact (Lead DM role) for assigned clinical project(s) / program(s), ensuring that there is back-up, continuity, responsiveness, and that tasks are performed in a timely manner. May support another Lead DM as a back-up and/or team member. May include DM oversight of sponsor programs.
Oversee project data entry process including development of data entry guidelines, training, data entry quality and resourcing
May perform quality control of data entry
Provide input, assesses and manage timelines. Ensure that clinical data management deadlines are met with quality. Assess resource needs for assigned projects, as needed.
Develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders
May assist in building clinical databases
Conduct database build UAT and maintain quality controlled database build documentation. Oversee overall quality of the clinical database.
May specify requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. Oversee development of the edit check specifications and manual data review specifications
Responsible for creating, revising, appropriate versioning and maintaining data management documentation. Oversee completeness of data management documentation for the Trial Master File.
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
May require some travel
Perform other duties as assigned

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 29 days 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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