Job Summary:  

The Senior Clinical SAS Programmer is responsible for building computational programs to create SAS datasets and data listings from clinical study databases and external data sources. This role will determine desired specifications of use for data reviewing and cleaning via collaboration with cross-functional members from, Data Management, Drug Safety, and Clinical Development. This position requires high degree of independence, technical skills and ability to produce outputs.

Essential Duties & Responsibilities:

Assists data managers to ensure clinical study database quality. Assists data managers in edit checks, eCRF annotations, and data specifications. Creates SAS data listings and study data reports for clinical study data cleaning/validation. Creates clinical study/project tracking reports (e.g., enrollment summary report) Creates data listings for data reconciliation (e.g., AEs, SAEs, safety laboratory, medical coding) Assists developers to build an in-house analytical visualization tool (Trial Insight) for interactive data visualization and data automation. Assists functional leads to maintain and improve standards and processes. Keeps up to date on all study specific trainings and industry standards. Performs other study/project related duties as assigned.

Supervisory Responsibilities:

N/A

Knowledge & Other Qualifications:

Bachelor’s degree in computer sciences, biostatistics, statistics, mathematics, life sciences, or other related field with a minimum of four years of experience in the pharmaceutical, Biotechnology, or clinical research organization industry or a master’s degree with two or more years of experience Fluent in SAS data step programming including SAS macros. Knowledge of Clinical Data Management processes and systems preferred. Knowledge of computational programs (e.g., Power BI) for static and interactive data visualization Excellent attention and accuracy with details Excellent verbal communications and written skills Ability to work in team situations. Ability to handle multiple tasks and projects. Ability to work in a fully self-directed manner. Knowledge of ICH/GCP rules and regulations

Other Characteristics:

Ability to work independently and as part of a team and maintain high ethical standards of integrity and quality. Ability of having an innovative and dynamic approach to work. A self-starter able to work independently but comfortable working in a team environment. Ability to consistently exhibit Supernus Values in interactions with employees at all levels of the organization, vendors, customers, and others. Capable of performing other duties as assigned by Management. Authorized to legally work in the United States without visa sponsorship.

Physical Requirements/Work Environment/Travel Requirements:

Sedentary work. Exerting up to 10 pounds of force occasionally and/or carrying objects. Sedentary work involves sitting most of the time. The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer screen, iPad, or other electronic device; and extensive reading. The worker is not substantially exposed to adverse environmental conditions.

Compensation:

At Supernus, we offer a competitive compensation package that reflects your experiences and contributions.  The expected salary range for fully qualified candidates applying for this role is $90,000 to $110,000. This range is what the Company reasonably expects to offer for the position and is not reflective of the full compensation scale of the role. This range may be modified in the future. An individual’s salary within the range is based on multiple factors, which may include and are not limited to education, relevant experience, knowledge, length of industry experience and organizational needs.  

Base salary is one part of the overall compensation package, which includes the opportunity to participate in employee stock purchase programs and performance-based bonus programs.

 

Supernus Pharmaceuticals is an award-winning biopharmaceutical company with more than 30 years of experience in developing and commercializing products that treat central nervous system (CNS) diseases. At Supernus, we develop innovative products that help treat neurological and psychiatric conditions. We currently have 8 products in the market that are making a real impact on patient outcomes.

 

Supernus Pharmaceuticals is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, age or any other characteristic protected by law.