Principal Statistical Programmer - remote
Company: Precision Medicine Group
Location: San Diego
Posted on: May 15, 2022
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Job Description:
Why should you considering joining us? Because Precision for
Medicine is not your typical CRO. As a member of our thriving team,
opportunities to work with leading subject matter experts who
understand the rare disease patient mindset and experience will
surround you. We help translate science into success for rare
disease patients with a targeted, patient-centric approach over a
wide geographic area. We are specialists who tackle unusual
problems in our detailed approach throughout every phase. From the
beginning, we have nurtured a culture where patients' needs and the
needs of our valued clients come first. We focus in an environment
where the quality of our work is the best, and where our employees
can thrive, while still having fun and giving back to the patient
community.
We welcome your voice and opinions and provide you with the ability
to truly make an impact on investigational product development. Are
you ready to be part of a close-knit clinical trial team that is
passionate about saving the lives of patients every single day?
Then look no further, we'd like to help you take your career to the
next level. If the duties below sound like a fit, we'd love to hear
from you!
About You
You are passionate about health care solutions in rare disease and
oncology
You thrive in a fast paced environment while maintaining a high
level of quality
You love working on a team and providing collaborative input to
others, working well with data and project management
You are comfortable interpreting, communicating and presenting
statistical results to non-statisticians providing explanations and
answering the statistical or clinical questions to
non-statisticians in simple terms
You are a strong SAS programmer, experienced in supporting the
analysis of clinical trial data
You have excellent written and verbal communication skills
What To Expect Day To Day
Create specifications for derived/analysis datasets
Program analysis datasets, tables, figures, and listings to support
the analysis of clinical trials data using SAS
Generate SDTM domains, ADaM datasets, and Define.xml files
Provide programming support to supplemental or exploratory analyses
for regulatory agencies or any other internal and external ad-hoc
requests
Perform quality control for SAS programs and other study documents
(e.g., presentations and reports)
Document the quality control review process
Review output across programs to ensure consistency
Review, maintain, and approve study documents per standard
procedures
Program, test, and document global utility programs and tools in
accordance with standards and validation procedures
Provide technical oversight and leadership in the areas of analysis
and reporting
Participate in the development and/or maintenance of departmental
procedures and standards
Assist in creation of table mockups under supervision of
statisticians
Serve as the primary project team representative, delegating work
as appropriate
Train and mentor new programmers
Qualifications
Minimum Required: BS degree in Statistics, Mathematics or Computer
Science or in a related field
Other Required
Principal Statistical Programmer: Minimum 8 years
Biotechnology/Pharmaceutical/CRO industry experience as a clinical
trial Statistical Programmer
Senior Lead Statistical Programmer: Minimum 7 years
Biotechnology/Pharmaceutical/CRO industry experience as a clinical
trial Statistical Programmer
Senior Statistical Programmer: Minimum 5 years
Biotechnology/Pharmaceutical/CRO industry experience as a clinical
trial Statistical Programmer
Preferred
SAS Certified Advanced Programmer for SAS 9 or equivalent
proficiency
Base SAS -, SAS/STAT and SAS/ACCESS software
Advanced computer skills
Demonstrates extensive knowledge with industry standards, such as
the ICH guidelines, CDISC data structures, 21 CFR Part 11, and FDA
guidelines
Excellent organizational skills, time management, and ability to
coordinate workload and meet established deadlines
Excellent communication and interpersonal skills to effectively
interface with others
Proficient in SAS Macro Programming
Any data provided as a part of this application will be stored in
accordance with our Privacy Policy .
Precision Medicine Group is an Equal Opportunity Employer.
Employment decisions are made without regard to race, color, age,
religion, sex, sexual orientation, gender identity, national
origin, disability, veteran status or other characteristics
protected by law. - 2020 Precision Medicine Group, LLC
If you are an individual with a disability and require a reasonable
accommodation to complete any part of the application process, or
are limited in the ability or unable to access or use this online
application process and need an alternative method for applying,
you may contact Precision Medicine Group at
QuestionForHR@precisionmedicinegrp.com .
Keywords: Precision Medicine Group, San Diego , Principal Statistical Programmer - remote, IT / Software / Systems , San Diego, California
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