<p>The Opportunity</p> <p>The Clinical Data Management team at Amylyx Pharmaceuticals is seeking an Associate Director, Clinical Data Programmer. This individual will work collaboratively cross-functionally to provide hands-on data management support, programming support and technical leadership to develop, maintain, validate the clinical database, and run computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. As an Associate Director of Clinical Data Programming, you will be required to program in the appropriate languages to create both textual and graphic displays that facilitate data cleaning and review.</p> <p>Responsibilities</p> <ul> <li>Lead the study-specific design, development, and validation of study clinical data capture systems, ensuring data integrity, CDISC compliance and CRO oversight. </li><li>Supports leading data management activities (i.e. DMP creation, CRF creation, edit checks creation, database lock), assisting with database setup, conduct and closeout phases. </li><li>Performs UAT of systems and ensures appropriate plans and documentation are in place. </li><li>Leads the development of SAS macros, data listings, summary tables and visualizations for supporting periodic and ad hoc data review. </li><li>Manages external vendor compliance and quality checks. </li><li>Supports Clinical Operations, Biostatistics and Data Management by providing data insight and solving technical data challenges. </li><li>Ensures databases adherences to SOPs, 21CRF Part 11, ICH-GCP and CDISC Standards (CDASH/SDTM) </li><li>Acts as a subject matter expert in leading technical initiatives and data management </li></ul> <p>Required Qualifications</p> <ul> <li>Bachelor's degree or higher in Life Science or related discipline </li><li>8+ years of experience in clinical data management </li><li>Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python </li><li>Proven experience in clinical trial programming and database management </li><li>Knowledge of Clinical Data Standards such as CDISC CDASH, and SDTM </li><li>Provide strong support to Data Management </li><li>Experience creating advanced interactive data visualizations from raw data using multi-languages and applications such as Using SAS, R, Python, RShiny, Power BI, Tableau, Spotfire etc. </li><li>Ability to manage multiple projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change. </li><li>Excellent written and verbal communication skills and organizational and documentation skills. </li></ul> <p>Work Location and Conditions</p> <ul> <li>At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee. </li><li>You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested, which may include travel by air, driving or public transportation. </li><li>You must have access to work in setting that meets all requirements of the role (including privacy, reliable internet access, phone, ability to communicate via video conference, etc.) at your remote locatio </li></ul>