A Biostatistics Manager or Director manages a team of statisticians and directs statistical analysis and reporting of health and biology-related data. Analysis may be used for product development at a pharmaceutical company, disease research at a hospital or health policy research at a public health organization. Directs the design of statistical analysis and reviews analysis and findings; may manage regulatory reporting for projects such as clinical trials.
$160,510 / year median in Washington, D.C. (District of Columbia)
Biostatistical Programming Manager Employer Amgen Location Washington D.C., District of Columbia Start date Jul 24, 2026 View more categories View less categories Discipline Information Technology , Science/R D , Biostatistics Required Education High School or equivalent Position Type Full time Hotbed Best Places to Work Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details Join Amgens Mission of Serving Patients At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do. Since 1980, weve helped pioneer the world of biotech in our fight against the worlds toughest diseases. With our focus on four therapeutic areas Oncology, Inflammation, General Medicine, and Rare Disease we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, youll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Biostatistical Programming Manager What you will do Lets do this. Lets change the world. In this vital role you will provide both strategic oversight and hands-on statistical programming support to enable high-quality and timely clinical trial deliverables. This role is part of the centrally managed Quality and Quick Response (QQR) Programming team and is responsible for supporting urgent and high-priority programming needs across development programs. The manager will serve as a technical programming expert who can rapidly respond to internal and external requests, support special projects, provide global quality oversight, and contribute directly to programming deliverables when needed. This role will primarily support programs within the Obesity Therapeutic Area and requires close collaboration with cross-functional teams to support fast-paced development activities and evolving business priorities. Responsibilities Provide rapid response statistical programming support for urgent internal and external requests Serve as a lead programmer for studies and projects, such as Data Access Plan (DAP) activities, unblinding efforts, and special projects Deliver hands-on programming support for SDTM, ADaM, Tables, Listings, and Figures (TFLs), and other study and regulatory submission deliverables as needed Oversee the execution and quality of projects managed by our FSP partners per Amgen Global Statistical Programming (GSP) Quality Oversight Plan (QOP) Ensure that FSP and in-house programming deliverables meet quality, compliance, timeline, and productivity expectations Mitigate at-risk projects by providing technical expertise, programming support, and operational guidance Contribute to training material development and delivery to internal teams and FSP partners Provide guidance and technical consultancy to study programming team on Amgen processes, tools, and utilities Lead/contribute to GSP continuous improvement iniatives and support cross-functional initiatives including inspection readiness, process improvement, innovation, and training activities Contribute to programming team performance metrics development, data collection, and reporting Review project documentation such as specifications, issue logs, deliverable status for accuracy and completeness What we expect of you We are all different, yet we all use our unique contributions to serve patients. The dynamic professional we seek is a manager with these qualifications.
Basic Qualifications:
Doctorate degree OR Masters degree and 2 years of statistical programming experience OR Bachelors degree and 4 years of statistical programming experience OR Associates degree and 8 years of statistical programming experience OR High school diploma / GED and 10 years of statistical programming experience
Preferred Qualifications:
Masters in Statistics, Mathematics, Computer Science, Life Sciences or another relevant scientific subject 6+ years of statistical programming in biopharmaceutical industry Regulatory submission experience Strong hands-on SAS programming expertise including SAS Base, Macro, SQL, SAS/Graph and Stat packages Experience with R programming for clinical trial analyses, data manipulation, reporting and visualization preferred Familiarity with additional programming languages and tools such as Python preferred Hands-on experience developing and validating SDTM, ADaM datasets, and TFLs Thorough understanding of clinical trial processes from data collection through analysis and reporting Ability to lead programmers in successful completion of all study programming activities and provide guidance on technical and process questions Strong understanding of data standards and compliance checks including Pinnacle 21 Experience providing quality oversight for outsourced and internal programming deliverables Ability to troubleshoot complex technical issues and turnaround at-risk projects Experience working in a globally dispersed team on Phase 1-4 clinical trials Experience supporting clinical development programs within the Obesity Therapeutic Area preferred Understanding of obesity clinical endpoints, data standards, and regulatory considerations is highly desirable Excellent oral and written English communication skills; strong collaboration, negotiation, and organizational skills What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, well support your journey every step of the way. The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $130,000 to $140,000. Actual salary will vary based on several factors including, but not limited to, relevant skills, experience, and qualifications. In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan Stock-based long-term incentives Award-winning time-off plans Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies. Apply now and make a lasting impact with the Amgen team. careers.amgen.com In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information. Company We are all different, yet we have this in common: our mission to serve patients. This sense of shared purpose is key to our becoming one of the world's leading biotechnology companies. It guides us as we continue to launch new medicines and reach millions of patients worldwide. We live the mission. We win together. We thrive on continual challenge. Our team of 22,000+ scientists and professionals worldwide bring distinct perspectives and experiences to all we do. We leverage our global talent to achieve together—to research, manufacture and deliver ever-better products and greater depth to our mission. At Amgen, there is a strong correlation between our high level of diversity and performance. Because addressing issues with a wider range of perspectives and approaches leads to more creative problem-solving. Together, we're transforming the promise of science and biotechnology into therapies that have the power to restore health. Connect with us to explore how you can Win, Live, and Thrive at Amgen.
Company info Website http:
//careers.amgen.com/ Phone 805-447-1000 Location Corporate Headquarters One Amgen Center Drive Thousand Oaks California 91320-1799 United States Share this job Facebook Twitter LinkedIn Apply now Send job Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Get job alerts Create a job alert and receive personalized job recommendations straight to your inbox. Create alert Similar jobs Senior Manager, Clinical Data Systems Florham Park, NJ Sr. Director, Biostatistics & Statistical Programming Malvern, PA Specialist, External Data Acquisition and Delivery Hyderabad, India