For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs.
Essential Functions:
Provide statistical programming and validation for life sciencesrelated projects including clinical trial datasets and tables, listings,
and figures.
Access and convert data to SAS datasets and other file types from
database management system and PC file formats (e.g., Microsoft
Excel, text files).
Work with external vendors to develop and/or monitor the content and
structure of SAS datasets and other files.
Work closely with statisticians and other statistical programmers to
generate and validate outputs to ensure accuracy and ensure the
quality and soundness of statistical programming algorithms.
Provide input to specifications of tabulation and analysis datasets,
validation plans, and other related documents
Other duties as assigned.
Necessary Skills and Abilities:
In-depth knowledge of statistical programming.
Excellent communication and interpersonal skills, with the ability to
work collaboratively in cross functional teams and with external
partners.
Ability to program in SAS and/or R preferred.
Educational Requirements:
Bachelor’s degree in Statistics, Computer Science, Mathematics, or a
related discipline, or a combination of other education with 1+ years
of relevant work experience.
Experience Requirements:
Experience with CDISC data structures, such as SDTM and ADaM.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Top Skills
What We Do
ProPharma is the premier Research Consulting Organization (RCO), delivering fully customizable consulting solutions to empower biotech, med device, and pharmaceutical organizations of all sizes to advance scientific breakthroughs confidently and introduce new therapies.
With over 20 years of expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma partners with clients across the complete product lifecycle through an advise-build-operate model. Our end-to-end suite of consulting solutions de-risk and accelerate high-profile drug and device programs, ultimately improving patient health and safety. Discover how ProPharma can help you inspire the future of science
