Associate Director, Clinical Data Programmer

Amylyx Pharmaceuticals • Cambridge, MA

1d • Remote

About The Position

Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS). Our mission is powered by our people. Our core values – be audacious, be curious, be authentic, be engaged, and be accountable – creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine’s toughest problems, we encourage you to read the opportunity below and apply. The Opportunity 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.

Requirements

• Bachelor’s degree or higher in Life Science or related discipline
• 8+ years of experience in clinical data management
• Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python
• Proven experience in clinical trial programming and database management
• Knowledge of Clinical Data Standards such as CDISC CDASH, and SDTM
• Provide strong support to Data Management
• 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.
• Ability to manage multiple projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change.
• Excellent written and verbal communication skills and organizational and documentation skills.

Responsibilities

• Lead the study-specific design, development, and validation of study clinical data capture systems, ensuring data integrity, CDISC compliance and CRO oversight.
• Supports leading data management activities (i.e. DMP creation, CRF creation, edit checks creation, database lock), assisting with database setup, conduct and closeout phases.
• Performs UAT of systems and ensures appropriate plans and documentation are in place.
• Leads the development of SAS macros, data listings, summary tables and visualizations for supporting periodic and ad hoc data review.
• Manages external vendor compliance and quality checks.
• Supports Clinical Operations, Biostatistics and Data Management by providing data insight and solving technical data challenges.
• Ensures databases adherences to SOPs, 21CRF Part 11, ICH-GCP and CDISC Standards (CDASH/SDTM)
• Acts as a subject matter expert in leading technical initiatives and data management

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level