Job Vacancies

MaxisIT is seeking an experienced R&D Solutions Business Partner to drive strategic business development of Statistical Computing Environment (SCE) and tech-enabled statistical programming services among biostatistics and statistical programming decision-makers across pharmaceutical, life sciences, and medical device companies conducting clinical trials. This role acts a bridge between MaxisIT’s sales and customers’ biostatistics programming and IT teams.

We’re excited to announce an opportunity for a Team Leader Real World Data at the Danone Nutricia Research & Innovation (R&I) Center, located in Utrecht, the Netherlands. Our team operates at the dynamic intersection of life sciences, digital health, clinical operations, medical affairs, and biometric data science within our Global R&I Medical & Nutritional Sciences division.

The Associate Director is responsible for leading statistical programming efforts for a busy research center, collaborating with internal and external collaborators in the creation, implementation and maintenance of statistical programming infrastructure and deliverables. The Associate Director will lead the effort to continuously improve programming processes to conform to evolving industry standards and participate in the ongoing review and development of quality systems and processes.

Location: Boston, MA

Lead efforts in resolving day to day work related issues and problems, securing quality, improving efficiency and productivity of statistical and programming operations. Lead assigned projects by applying project management skills, statistical and programming techniques; achieve quality and on time delivery of deliverables, earn client’s trust and repeat business. May take on the role of a Lead Biostatistician for a developmental program with more than one or two trials, leading other Biostatisticians and coordinating activities with project/program overall.

The Senior SPA I is an independent statistical programmer analyst supporting the clinical reporting production programming and verification for client regulatory submissions and publications. Critical client project activities are reporting database development (SDTM and ADaM), statistical and clinical reporting, verification, and submissions support.