$80,000–$100,000 Per Year
Intern, Volunteer, Full-time
Statistics, Statistical Analysis System (SAS), Python Programming/Scripting Language, Analysis Skills, Clinical Data Interchange Standards Consortium (CDISC), SDTM, Biometrics, Biostatistics, Clinical Research, Clinical Trial, Clinical Trial Management, Cross-Functional, Statistical Programming Languages,
- Basic to intermediate proficiency in SAS programming is required (experience with Base SAS or SAS/STAT). Familiarity with R or Python is a plus. We provide ongoing training for the right candidate.
- Bachelor’s degree in Biostatistics, Epidemiology, Public Health (MPH), Statistics, Health Informatics, or a closely related biomedical/quantitative field.
- 0 to 2 years of experience in clinical research, pharmaceutical industry, or academic research environments (Relevant internships or graduate-level research projects are highly valued).
- Solid understanding of basic statistical concepts and epidemiological study designs.
- Familiarity with clinical trial terminology and data standards (CDISC/SDTM/ADaM) is preferred but not required (training will be provided).
- Exceptional attention to detail and strong analytical mindset.
- Excellent written and verbal communication skills for a remote team environment.
- Strong time-management skills with the ability to handle multiple task deadlines.
- Basic to intermediate proficiency in SAS programming is required (using BASE/SAS, SAS/STAT, SAS/GRAPH and SAS MACROS for assigned clinical projects(s). Familiarity with R or Python is a plus. We provide ongoing training for the right candidate.
- Programs quality checks for clinical study raw data and report the findings to Data Management
- Produces and delivers CDISC and regulatory compliant SDTM, and ADaM standard datasets
- Creates and validates tables, figures and listings (TFLs) in a timely and high-quality fashion, consistently meeting objectives of the study, and regulatory requirements
Provides input in the design and development of case report forms and clinical databases - Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets, ADaM datasets and TFLs
- Reviews or author SDTM and ADaM datasets specifications for datasets programming
Provides programming support for adhoc analysis - Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g., macros or graphical user interface applications)
- Manages timelines and schedules of specific phases of projects
Performance Bonus, Flexible Schedule, Work From Home, Flexible Spending Accounts
ClinPharma Clinical Research LLC is a well-established clinical company recognized for long-term expertise in clinical trial management and biometrics
We are currently seeking a motivated, remote SAS Programmer to join our elite Biostatistics team. In this pivotal role, you will collaborate with cross-functional experts to deliver high-quality statistical programming deliverables that directly drive clinical trial success. If you are looking for an exciting career where you can leverage your existing expertise while accelerating your professional growth, this is the perfect opportunity for you.
C
ClinPharma Clinical Research LLC