This unique position offers an ambitious candidate the opportunity to contribute and learn through direct exposure to a wide spectrum of biometrics activities in support of Clinical Development, Regulatory Agency submissions and Medical Affairs activities.  The incumbent will be responsible for planning and executing a range of biostatistical activities to support design and analyses of clinical studies and their related medical affairs tasks. These responsibilities may also include ad hoc analyses of existing databases, study design simulation, meta-analyses, and data mining. Tasks include planning, programming, and executing statistical analyses; contributing to content and review of clinical study protocols, statistical analysis plans, clinical study reports, presentations and manuscripts; and occasional instructing and reviewing third party statistical planning and analysis work.

This is a hybrid position, 3 days per week, based in Waltham, MA.

Responsibilities

• Experience in the development of protocol, statistical analysis plans, programming, and analyses of Phase I-IV clinical trials
• In-depth experience of R, Base SAS,SAS/STAT, and SAS/GRAPH
• Excellent analytical, problem solving and organization skills with the ability to work simultaneously in multiple tasks
• Flexible to changing priorities, detail-oriented, works well under pressure and able to take on unfamiliar tasks
• Ability to work in a collaborative environment, desire to learn and improve skills
• Ability to communicate statistical information to non-scientists, willingness to educate internal teams
• Experience with standard statistical methods including but not limited to parametric and non-parametric analysis, survival analyses, longitudinal data analysis, logistic regression, methods used in handling missing data, MMRM, GEE, multiple testing procedures, multivariate statistics, meta-analysis and categorical data analysis
• Ability to apply innovative statistical approaches to the design of studies (e.g., modeling and simulations, adaptive design and/or Bayesian approaches) 
• Ability to guide data management and programming in developing standards for building databases, edit checks, and statistical programming for data analyses.
• Experience in managing statistical and programming activities of CROs  
• Experience in planning and preparation of integrated summary documents- ISE, ISS

Qualifications

• At least 4years of experience in pharmaceutical, biotech, and/or CRO setting
• Ph.D. in Biostatistics, Statistics or Applied Mathematics
• Ability to understand and develop statistical and patient-based models, using the latest tools and methodologies
• Strong analytical skills and demonstrated experience in gathering, interpreting and analyzing data
• Strong statistical experience in clinical research and drug development
• Experience in US and/or Non-US submissions
• Strong communication and interpersonal skills; ability to interact with cross-functional teams

Travel Expectations:

• Overnight travel ~10%

About Us

Why join Team Alkermes?

Alkermes applies its deep neuroscience expertise to develop medicines designed to help people living with complex and difficult-to-treat psychiatric and neurological disorders. A fully-integrated, global biopharmaceutical company, headquartered in Ireland with U.S. locations in Massachusetts and Ohio, we are committed to pursuing great science, driven by deep compassion to make a real impact in the lives of patients. Alkermes has a portfolio of proprietary commercial products for the treatment of alcohol dependence, opioid dependence, schizophrenia and bipolar I disorder, and a pipeline of clinical and preclinical candidates in development for various neurological disorders, including narcolepsy.

Beyond our important mission of developing medicines to address unmet patient needs, we actively seek to foster a culture of diversity, inclusion and belonging throughout our business. We strive to ensure that all voices are respected and valued, recognizing that our diversity of thought, background and perspective makes us stronger. We are proud to have been recognized as an employer of choice by many national organizations, including being certified as a Great Place to Work in the U.S. in 2024, honored as a Healthiest Employer in both Ohio and Massachusetts in 2023, a Best Place for Working Parents in 2023, and to have received the Bell Seal at the Platinum level for Workplace Mental Health by Mental Health America for three consecutive years (2021-2023). 

Alkermes, Inc. is an equal employment opportunity employer and does not discriminate against any qualified applicant or employee because of race, creed, color, age, national origin, ancestry, religion, gender, sexual orientation, gender expression and identity, disability, genetic information, veteran status, military status, application for military service or any other characteristic protected by local, state or federal law.  Alkermes also complies with all work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.  Alkermes is an E-Verify employer.