Department: Regulatory and Clinical Affairs

Job Title: SAS Programmer Analyst

Location: Andover, MA

TransMedics is a medical device company strategically positioned to improve outcomes for patients with end-stage organ failure. Today, these patients confront a serious shortage of organs compounded by clinical outcomes from organ transplantation that are often suboptimal, due to current methods of organ preservation. TransMedics Organ Care System (OCS) provides a life-support system for organs en route to transplant recipients. Continuously perfused with warm, oxygenated blood and maintained in a normal functioning state, the organs can travel further and arrive healthier. The receiving surgeon can assess the organ's functional status immediately prior to transplantation using monitoring equipment built into the device. In addition, the TransMedics OCS device represents a breakthrough advance due to the system's inherent ability to tap into the existing underutilized donor pool while improving clinical outcomes

The main purpose of this role is, as a member of the Regulatory and Clinical Affairs project team, to assist the team in delivering high quality SAS datasets, tables, listings and graphical reports to the project and management teams. This output is used to support regulatory submissions, publications and commercial activities. It will require you to be responsible for the quality of your own work and you will be expected to manage your own daily planning.

The ideal candidate will have 3-5 years of SAS programming experience within a Clinical setting and experience of working as part of a clinical project study team. Experience working with EDC databases as you will participate in setting up a new database.

Responsibilities:

• Performs complex design and programming tasks. Requires interfacing with inter-departmental project team members and management team.
• Write and debug statistical programming in SAS to check and process data, generate tables, analyses, graphs, and data listings with an emphasis on the most programmatically challenging sections of the analysis system.
• Insure that project-specific derived dataset specifications and analysis programming specifications are complete and accurate.
• Coordinate project-specific statistical programming resources including defining timelines for batches of data displays in conjunction with the team and reviewing programming code.
• Conceptualize, design, and implement programs and processes to standardize statistical programming across projects. Participate in setting up a new database.
• Participate in the design of logic checks, data collection guidelines, information flow, analysis plans, and reports for clinical studies.
• Learn standard coding classification systems used for coding of medical procedures, medications, and serious adverse events.
• Attend project meetings to present status reports on accrual, case eligibility, dropouts, exclusions, adverse events, safety, data quality, information timeliness, and problem data.
• Interact with Data Manager, Monitors, other team members and Management.

Join us, and help bring the gift of life to patients in need around the world. Along with an exceptional culture, we offer a competitive compensation and benefits package, an entrepreneurial environment, and the opportunity for employees to enhance their careers and achieve greater levels of responsibility as the company grows. TransMedics is an Equal Opportunity Employer. For more information please visit our website at www.transmedics.com.

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