When our values align, there's no limit to what we can achieve. parexel fsp is seeking to hire multiple senior statistical programmers to join our team. the candidates could be based anywhere in argentina, mexico and colombia. the senior statistical programmer provides technical expertise for the conduct of clinical trials, acts as an internal subject matter expert in specific areas providing technical support and expert advice, and works independently to support various programing activities related to the analysis and reporting of clinical study data. in addition, the senior statistical programmer can fill the statistical programming lead role on projects, and liaise with sponsors, biostatistics leads, data management leads, and other functional areas as required. further, the senior statistical programmer will monitor quality, timelines, resource allocation, and productivity in relation to budgets. key accountabilities: project management: ability to fill statistical programming lead role on projects -input into and negotiate statistical programming timelines. ensure that timelines are adhered to. -coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget. -monitor project resourcing, project budgets, and identify changes in scope. coordinate project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation. review statistical analysis plans and mock-shells. review database set-up specifications. interact with sponsors and internal stakeholders with regard...
Do you know why we are one of only three cros to have received the leadership award for 11 consecutive years? because we appreciate our team, whose dedication and commitment to excellence is reflected in this award, and we work with heart, keeping the patient at the center of everything we do. join our team and develop your career with us by contributing your personal and professional talents and skills. together we will continue to do things that matter to people. parexel fsp is looking for a site monitor in spain (madrid or barcelona) to strengthen our clinical operations team. work from home and with the flexibility you want. our sms have less travel and less workload to maintain work-life balance. we offer long-term projects, world-class technology, and training tailored to your individual experience. as a sm, you will work independently and will be responsible for all activities required to set up and oversee a study, complete study status reports, and maintain study documentation. you will participate in the submission of protocols, consent documents for ethics / irb approval, and assist in the preparation of regulatory submissions as requested. you will have the opportunity to be a unique sponsor dedicated to one of the top 10 pharmaceutical companies in the world, working on oncology studies that deliver real impact. minimum requirements: bachelor's degree in a life science or related discipline. minimum of 3 years' experience in independent site monitoring - all types of visits. understanding of ich gcp compliance. excellent time management and social skills. highl...
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