800 million! Thats the number of lives we impact around the world through innovative products and cutting-Edge medical science, novartis is among the worlds leading pharmaceutical companies, always seeking to bring innovative products to patients quickly and effectively. As a global company, resources and learning opportunities at novartis are also plentiful, involving both global and local cross-Functional careers. As part of novartis brazil, you will have great opportunities to develop and impact the success of our business, contributing to the same purpose of reimagining medicine to improve and extend peoples more information about novartis access (Informação Confidencial) and (Informação Confidencial) your responsibilities:at novartis we want everyone to be able to be their best version, both in the work environment and in their personal lives. Therefore, we are continually evolving our way of clinical trial project consultant position is eligible for the hybrid working model (face-To-Face and virtual). At novartis, teams have the autonomy to decide the best flexible working format, balancing team collaboration, team impact on novartis business, and employee well-Being. Further details regarding working model will be explained throughout the selection responsibilities include, but are not limited to:Leads and coordinates the execution of a clinical trial from study start-Up (including protocol, icf and ecrf development) through database release/study closeout and inspection readiness to ensure timely delivery of quality study leadership to the teams in the setting of site selection, realistic recruitment targets, budget management and delivery milestones as the single point of accountability for detailed study start-Up and monitoring plans and for delivery to the agreed with functional lines and directly with cro line functions to resolve or triage site level issues. The study manager will drive decision making and work closely with the clinical study team lead to provide input to operational staff fulfill their responsibilities by being co-Responsible for implementation and complying with standards (sops) and best practices for clinical operations/clinical data review activities of assigned studies/programs, including sharing lessons learned. Diversity & inclusion / eeo what youll bring to the role:Health degree is in the regulatory framework of a clinical experience monitoring clinical of gcp regulations, project management, and new methodologies, experience in effective crisis management and risk level of english is to receive:competitive salary, annual bonus, pension scheme, life insurance, 30 days annual leave, year-End recess, hybrid work model (home office 2x a week), flexible working arrangements, birthday day-Off, maternity and paternity leave, subsidized dining facilities, health and dental insurance, employee recognition scheme, free parking lot (santo amaro and cambe), gympass, space energized for life, gym (santo amaro) and virtual self-Development consider novartis?236 million lives were touched by novartis medicines in 2022, and while were proud of this, we know there is so much more we could do to help improve and extend peoples lives. We believe new insights, perspectives and ground-Breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent whats possible, when we collaborate with courage to aggressively and ambitiously tackle the worlds toughest medical challenges. Because the greatest risk in life, is the risk of never trying!Imagine what you could do at novartis!Join our novartis network: if this role is not suitable to your experience or career goals but you wish to stay connected to hear more about novartis and our career opportunities, join the novartis network here: (Informação Confidencial).
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