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STATISTICAL PROGRAMMER II - FSP

When our values align, there's no limit to what we can achieve. parexel fsp is seeking to hire multiple statistical programmers ii to join our team. the candidates could be based anywhere in argentina, mexico and colombia. the statistical programmer ii provides technical expertise for the conduct of clinical trials, and works with minimal supervision to support various programming activities related to the analysis and reporting of clinical study data. in addition, the statistical programmer ii may fill the statistical programming lead role (or part of that role) on small, non-complex projects. project management: assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation. statistical programming for assigned projects: deliver best value and high quality service. check own work in an ongoing way to ensure first-time quality. use efficient programming techniques to produce derived datasets (e.g. sdtm, adam), tables, figures, and data listings of any complexity and qc low-medium complexity derived datasets, tables, figures, and data listings. assist in the production/qc of derived dataset specifications and other process supporting documents and submission documentation. training: maintain and expand local and international regulatory knowledge within the clinical industry. develop knowledge of sas and processes/procedures within other parexel functional areas. provide relevant training and mentorship to staff and project teams as appropriate. general: maintain all supporting docum...


(UBO-789) | REGULATORY AFFAIRS ASSOCIATE

As part of parexel consulting, you will create and maximize value for clients throughout the product lifecycle. you will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical device companies large and small. in return, you will be provided with interesting opportunities for growth and development and exposed to a variety of challenging assignments, product types, geographic regions, and therapeutic areas. plus, as member of parexel consulting, you will enjoy all the advantages of working remotely, combined with access to the mentorship from a team of highly experienced regulatory professionals at the height of their careers. join our team, and you will design solutions for the complexities of an ever-changing global marketplace. - full time - travel: yes - glassdoor reviews and company rating **success profile**: check out the top traits we're looking for and see if you have the right mix. - detail-oriented - proactive - problem-solver - results-driven - organized - multi-tasker **rewards**: - **global impact**: we are one truly global team working together to propel each client´s journey ahead faster. - **balance**: we value work-life balance. we try and keep regular hours and an emphasis on life outside the office. - **freedom**: the ability to innovate, ask “what if” and try new solutions without fear of failure. - **variety**: opportunities to work on multiple accounts ...


CLINICAL OPERATIONS ASSISTANT | W296

Join parexel’s team of changemakers as we help advance healthcare throughout the globe, all while keeping the patient at the heart of everything we do. **job title** clinical operations specialist at parexel, we are a leading clinical research organization (cro) company specializing in delivering life - changing medicines to patients. we are seeking clinical operations assistants to join our latin american team. as a clinical operations assistant, you will be joining a fast-paced, driven environment that is helping to make life-changing difference to patients. the role of the clinical operations assistant (coa) is to support clinical research associates and assigned project team with administrative tasks, site payments, management of site supplies, trial master file related tasks, and limited site facing tasks to support the efficiency, accuracy, and quality of the trials. through the collaboration, and diversity, of teams the clinical operations assistant is provided with multiple opportunities to excel and discover where your skills can take you. **what you will do**: - tracking, scanning, filing, entry and return of case report forms to clients for assigned projects. - managing documents in the electronic document management system - may have limited contact with investigator sites in context of supporting cras. **who we are looking for**: your study site experience and strong english and ms office skills will have prepared you for this fast-paced position. you have the flexibility to perform multiple tasks and ability to prioritize these to achieve proje...


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