Senior Statistical Programmer - Remote (US)
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-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 rate. We 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. Visit or follow MMS on LinkedIn . Applicants must be legally authorized to work in the U.S. for any employer; we cannot sponsor visas (e.g., H-1B) or offer work authorization transfers at this time. Job Specific Skills:
- Mastery and trained on generating 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, define.xml, Reviewer's Guides, SDSP.
- Lead study or small programming project teams.
- Masters required for all Statistics roles.
- Minimum of 5 years’ experience in Statistical Programming or similar field required.
- Expert knowledge of scientific principles and concepts.
- Reputation as emerging leader in field with sustained performance and accomplishment.
- Proficiency with MS Office applications.
- Hands-on experience with clinical trial and pharmaceutical development preferred.
- Good communication skills and willingness to work with others to clearly understand needs and solve problems.
- Excellent problem-solving skills.
- Good organizational and communication skills.
- Familiarity with current ISO 9001 and ISO 27001 standards preferred.
- Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
- Basic understanding of CROs and scientific & clinical data/terminology, & the drug development process.
Recommended Jobs
Property Tax Appeal Attorney
Pay: $140,000.00 - $200,000.00 per year Why This Is a Great Opportunity Join a highly regarded New Jersey law firm with a nationally recognized property tax practice Handle sophistica…
Chargeback Analyst II
We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or deliveri…
Physical Therapist-Outpatient- 13 weeks contract Assignment in Newark, NY
JOB SUMMARY The PHYSICAL THERAPIST (P.T.)- Outpatient is a qualified professional who directs, supervises, evaluates, and provides physical therapy services to patients as prescribed by the attendin…
Pet Nanny / Dog Walker - Florham Park, NJ
We’re looking for reliable, animal-loving folks to provide dependable pet sitting and dog walking (in the client's home). This role is perfect for fellow Pet Parents who enjoy being outdoors and carin…
WFH Digital Marketing Specialist
**WFH Marketing Specialist** **(Philippines-Based, US Hours)** **Location:** Remote – Philippines **Schedule:** Full-time, 40 hours/week with overlap to U.S. Eastern Time **Reports To:** Director…
Seasonal Director - Nature
Overview: The Nature Director is responsible for overseeing, leading, planning and implementing the Nature department. The Nature Director supervises 2-5 Nature Specialists as well as teaches…
Marketing Director - Thought Collect
Thought Collect is a New Jersey based strategic & creative marketing agency that loves food and technology. In that order. We're looking for an exceptional Marketing Manager to add to our team as …
Clinical Care Technician - Medical & Surgical X C2 - Full Time Night
Job Title: Clinical Care Technician Location: Monmouth Medical Center Department Name: Medical & Surgical X Req #: 0000210212 Status: Hourly Shift: Night Pay Range: $20.11 - $25.43 p…
Assistant Store Manager
Our values start with our people, join a team that values you! Bring your talents to Ross, our leading off-price retail chain with over 2,200 stores, and a strong track record of success and growth…
Quality Assurance Specialist
Location: New Brunswick, NJ / Central New Jersey (Hybrid Daily Local Travel Required) Employment Type: Contract Role (1099) About Us Were a fast-growing startup operating in specialized altern…