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Senior Statistical Programmer
2 months ago
Imagine how your expertise can change a patient's life. Our Clinical Affairs team generates extensive clinical evidence to demonstrate the effectiveness and safety of our innovations. As a Senior Statistical Programmer, you'll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need.
Key Responsibilities:- Develop, test, validate, document, maintain, and execute programs in SAS, serving as lead programmer.
- Provide programming expertise on one or more clinical trials in programming, documentation, validation, and review of summary tables, data listings, and graphs for inclusion in clinical reports or presentations.
- Lead in programming analysis datasets.
- Provide programming expertise on ad hoc data requests in collaboration with project statisticians.
- Develop program specifications and design documents in partnership with project statisticians.
- Ensure analysis data and programming code meet regulatory and company standards and are consistently structured to permit efficient programming, reporting, and review.
- Mentor, coach, and provide guidance to junior-level programmers.
- Collaborate with CDM to review draft CRFs, databases, and perform edit checks.
- Partner with clinical data management teams to ensure databases are defined consistently across clinical trials.
- Participate in the development of procedures, such as SOP development and standardization of output.
- Assist in compiling technical documents for internal and external audits.
- Bachelor's Degree in Statistics, Mathematics, Computer Science, or a related field, with 6 years of experience in statistical analysis.
- Master's Degree or equivalent in Statistics, Mathematics, Computer Science, or a related field, with 5 years of experience in statistical analysis.
- Ph.D. or equivalent in Statistics, Mathematics, Computer Science, or a related field, with 2 years of experience in statistical analysis.
- Proven expertise in MS Office Suite, including Word, PowerPoint, Access, and Excel.
- Excellent written and verbal communication skills and interpersonal relationship skills, including negotiating and relationship management skills.
- Keeps abreast of new developments in statistics and regulatory guidance.
- Extensive understanding and knowledge relevant to statistical programming.
- Proven expertise in SAS and Windows operating systems, with experience using other software packages, such as R, S-Plus.
- Extensive understanding and knowledge of regulatory guidelines, such as GCP, ICH, FDA, and ISO, relevant to pharmaceutical/medical device research settings.
- Excellent problem-solving, organizational, analytical, and critical thinking skills.
- Strong leadership skills and ability to influence change.
- Ability to provide training and coaching to lower-level employees.
- Experience in facilitating change, including collaboration with management and executive stakeholders.
- Strict attention to detail.
- Ability to interact professionally with all organizational levels.
- Ability to manage competing priorities in a fast-paced environment.
- Ability to work in a team environment, including serving as a consultant to management.
- Ability to interact with suppliers, vendors, and/or customers.
Edwards Lifesciences is an Equal Opportunity/Affirmative Action employer, including protected Veterans and individuals with disabilities. COVID Vaccination Requirement: Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement.