Senior Biometrics Informatics Consultant USDM Life Sciences - 3.0 Redwood City, CA Job Details Full-time $75 - $90 an hour 1 day ago Benefits Disability insurance Dental insurance 401(k) Paid time off Vision insurance Life insurance Qualifications Data systems development Requirements design GxP Clinical development Software implementation Git Enterprise solutions implementation Technical solutions implementation Bachelor's degree Pharmaceutical company experience Requirements analysis System requirements definition Standard operating procedures (SOPs) Statistical analysis tools

Full Job Description Job Title:

Senior Biometrics Informatics Consultant Job Function:

Compliance SME Location:

Redwood City, CA - Hybrid About

USDM USDM

Life Sciences is a premier consulting company with 20+ years of experience assisting heavily regulated biotech, medical device, and pharmaceutical companies with their GxP technologies to accelerate growth. Our deep domain knowledge and technology expertise in life sciences business processes are what set us apart. From strategy to implementation and adoption, we have delivered thousands of GxP projects globally. As part of the USDM team, you have the opportunity to work with cutting-edge technologies through our many partnerships with companies like Microsoft, Google, Oracle, DocuSign, Box, and many more. From molecule to market, you will help connect technology, people, and data in new ways to generate real-time insights to improve business outcomes for USDM's clients. Are you ready to make an impact and drive real digital transformation in life sciences? Founded in Santa Barbara in 1999, USDM has grown to a progressive, global company with 300+ remote employees and offices throughout the US, Canada, and Germany. Nature and Scope of Job Work with Clinical Data Management, Statistical Programming, Biostatistics, and Clinical Pharmacology to envision, evaluate vendors, purchase, configure or build, and validate a new Statistical Computing Environment (SCE) that enables our Client to scale support for its growing clinical portfolio. Primary Responsibilities Lead requirements gathering and vendor evaluation for a new Statistical Computing Environment. Develop the current-state system and interface map and create the vendor-selection scorecard. Coordinate pilots, vendor selection, and purchasing activities. Lead solution configuration, implementation, and validation with internal teams and vendors. Serve as the technical lead and subject-matter expert throughout implementation and handover. Additional Responsibilities Performs other related duties and assignments as required Qualifications Five or more years leading or supporting Statistical Computing Environment implementations in the drug-development industry. Experience leading vendor selection and implementation of validated systems in biotech or pharmaceutical environments. Strong knowledge of SAS and R programming practices in clinical development. Experience gathering requirements from Biostatistics, Statistical Programming, and Clinical Pharmacology teams. Experience working in GxP environments, including computer system validation and SOP-driven processes. Databricks experience. Clinical data standards experience. Git experience. Experience with AI-assisted SAS or R coding. Education & Certifications Bachelor's degree in Computer Science or Information Systems or related field. Master's Degree preferred Working Conditions The working conditions described here are representative of those that must be met by an employee to successfully perform the essential responsibilities and functions of the job and are not meant to be all-inclusive. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential responsibilities and functions of the job. Unless reasonable accommodations can be made, while performing this job the staff member shall: Prolonged periods of sitting or standing at a desk and working on a computer in an environmentally controlled home office environment. Operate other office productivity machinery, such as a calculator, scanner, or printer. Frequently communicate with stakeholders via telephone, email, or instant message. Must be able to exchange accurate information in these situations. Equal Opportunity Statement USDM Life Sciences is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Disclaimer This job description is intended to describe the general nature and the level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. USDM Life Sciences reserves the right to amend and change responsibilities to meet business and organizational needs as necessary. Compensation Salary/Hourly Rate Range (W2):

USD 75.00 - 90.00

The base salary/hourly rate range represents the anticipated low and high end of the USDM's compensation range for this position. Actual salaries/hourly rates will vary and will be based on various factors, such as the candidate's qualifications, skills, competencies, and proficiency for the role. The compensation described above is subject to change and could be higher or lower than the range described based on market survey data or budget. Full-time employees are eligible for health, vision, and dental insurance, life insurance, short and long-term disability, hospital indemnity, accident, and critical care coverage. Both full and part-time employees, who are at least 21 years of age, are eligible to participate in USDM's 401k plan. Full and part-time employees may be eligible for paid time off. All employees are eligible for USDM's rewards and recognition program.