Senior Statistical Programmer Remote (US)

About MMS

Are you looking to join a company where your contributions truly matter and where youll be part of a supportive innovative teamMMS is aaward-winning data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization recognized for our exceptional culture and industry best employee retention support the pharmaceutical biotech and medical device industries with our proven scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. follow MMS on LinkedIn.

Job Specific Skills :

• Mastery and trained ongenerating tables listings and graphs from clinical trial databases using SAS.
• Utilizes System Development Life Cycle (SDLC) for programming deliverables.
• Advanced user in SAS programming SAS Base and SAS Macros.
• Advanced knowledge of E-Submission Standards Guidelines and Regulations.
• Mastery and trained on SDTM standards including ability to write specifications.
• Advanced knowledge of ADaM standards including supporting specification writing.
• Proficient with MS Office applications.
• Advanced knowledge of ICH 21CRF Part 11 and ISO 9001 : 2000 requirements.
• Advanced experience with pooling of data sets for submissions.
• Advanced experience with BIMO outputs Reviewers Guides SDSP.
• Lead study or small programming project teams.

Job Requirements :

Required Experience :

Senior IC

Key Skills

Business Development,Customer Service,Attorney,CISSP,Data Analysis

Employment Type : Full-Time

Experience : years

Vacancy : 1