Statistical Programmer (SAS Programmer)

Join our innovative team at Integrated Resources Inc. as a Statistical Programmer (SAS Programmer). In this role, you will leverage your expertise in statistical programming to contribute to diverse projects within the pharmaceutical and healthcare sectors.Your responsibilities will include developing and validating SAS programs for data analysis, ensuring compliance with regulatory standards, and collaborating with cross-functional teams to deliver high-quality results.

At RAND Europe, a leading not-for-profit research institute with over 30 years of expertise, we conduct policy research aimed at addressing critical societal challenges. Our work for governments, international organizations, research councils, and charitable foundations is driven by our belief that thorough research can lead to informed answers that enhance community well-being, safety, and prosperity for the future. With offices in Cambridge, Brussels, and The Hague, we are proud to employ around 200 dedicated staff members.We are currently seeking a highly organized and detail-oriented Programme Support Officer to deliver exceptional support for numerous concurrent research proposals, projects, and frameworks managed by our expert research teams. This role will be based at our Cambridge office in the UK, requiring attendance twice a week.Key ResponsibilitiesLifecycle SupportManage the full project lifecycle from initial interest to final closure.Evaluate invitations to tender to ascertain regulatory and financial requirements for proposal submissions.Assist research teams in proposal development, including budget preparation and liaising with external stakeholders to gather necessary information and documentation, ensuring all required approvals are secured.Monitor project implementation to ensure milestones are achieved and objectives are met.Coordinate project closure activities, including final reporting, evaluation, and documentation.Financial ManagementReview and obtain approval for project budgets and proposals.Monitor, update, and maintain financial records for projects.Assist with variation requests, including changes to intercompany work authorizations.Corporate Governance, Quality Assurance, and ImprovementMaintain regulatory documents for all RAND Europe entities.Oversee governance for proposals and projects.Ensure entries in the lessons log are accurate and up to date.Develop, implement, and maintain processes and procedures related to functional and governance support.Contribute to continuous improvement of the Project and Finance Group's processes and practices.Support researchers in evaluating proposal and project effectiveness and impact.Adhere to all company policies and RAND Europe Management Systems.Ensure compliance with all IMS policies.Programme ManagementMaintain oversight of a portfolio of proposals, projects, and frameworks.Facilitate the transition of projects from proposal to execution and closure, ensuring effective completion at all stages.Track and report on project progress against milestones and objectives.

Are you passionate about infrastructure development and looking to take your career to the next level? AECOM is seeking an enthusiastic Associate Programme Manager to join our dynamic team in Cambridge. In this pivotal role, you will oversee and manage various infrastructure construction projects, ensuring they are executed on time, within budget, and to the highest quality standards.Your responsibilities will include collaborating with multidisciplinary teams, liaising with clients, and driving project success from inception through to completion. If you are a proactive individual with strong leadership skills and a desire to make a significant impact in the field of infrastructure, we want to hear from you!

Amylyx Pharmaceuticals is on a bold mission to revolutionize the treatment of diseases that have significant unmet needs. While others may see obstacles, we actively pursue opportunities with urgency, rigorous scientific methods, and a steadfast commitment to the communities we serve. As a clinical-stage company, we are currently targeting conditions such as post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS).Our mission is driven by our talented team, united by core values that include being audacious, curious, authentic, engaged, and accountable, fostering a culture of compassion. At Amylyx, we have assembled a highly experienced group dedicated to action, as the communities we serve cannot afford to wait. If you share our passion and are committed to addressing some of the most challenging problems in medicine, we invite you to explore this opportunity and apply.The OpportunityThe Clinical Data Management team at Amylyx Pharmaceuticals is in search of an Associate Director, Clinical Data Programmer. In this role, you will collaborate across functions to deliver hands-on data management support, programming expertise, and technical leadership. You will be responsible for developing, maintaining, and validating clinical databases, as well as executing computer programs to access, visualize, and report clinical trial data, adhering to clinical plans, ICH guidelines, and regulatory standards. As the Associate Director of Clinical Data Programming, proficiency in programming languages is essential for creating both textual and graphical representations that facilitate data cleaning and review.

Make an Impact at Lila Sciences As a pivotal member of our Physical Sciences division, you will spearhead the design and implementation of cutting-edge simulation methodologies aimed at modeling transport phenomena, kinetics, rare events, and reaction networks. Your innovative approaches will be integrated with artificial intelligence platforms to facilitate groundbreaking materials discovery. Your contributions will be essential in predicting, designing, and managing the behaviors of intricate materials and molecular systems, leveraging the power of agentic AI. Collaborating with our diverse teams, including experts in machine learning and materials science, you will help bridge theoretical research and practical experimentation. What You Will Create Enhance and develop molecular dynamics and Monte Carlo algorithms to effectively capture rare events, non-equilibrium processes, transport phenomena, and intricate reaction networks. Create scalable simulation workflows that merge statistical mechanics techniques with machine-learned interatomic potentials and agentic AI systems. Devise methods for synchronizing dynamic simulations with experimental observations to enable automated lab verification and discovery. Work collaboratively with computational scientists, machine learning specialists, and platform engineers to elevate the accuracy and scalability of simulation-driven material discoveries. Establish reproducible and modular software pipelines for statistical mechanics and dynamics simulations, optimized for high-performance computing and cloud environments. Qualifications for Success A PhD or equivalent research/industry experience in Physics, Chemistry, Chemical Engineering, Mechanical Engineering, Applied Mathematics, or related fields. A robust background in statistical mechanics, free energy calculations, reaction mapping, non-equilibrium dynamics, and rare-event sampling techniques. Proven expertise in molecular dynamics, Monte Carlo simulations, and/or kinetic simulation software frameworks (e.g., LAMMPS, GROMACS, OpenMM, HOOMD). Strong programming skills and experience in scientific computing (Python, C/C++, MPI, CUDA, etc.). Experience in executing and automating simulations on high-performance computing (HPC) and/or cloud platforms at scale. Bonus Qualifications A solid publication record showcasing the application of advanced statistical mechanics or dynamics simulations to molecular and materials systems, including molecular/biomolecular systems and solid-state materials and interfaces. Experience in integrating dynamics simulations with data-driven, AI-based, and/or agentic frameworks.