Clinical Trial Manager I with some experience in project management as a CTM or PM - Sao Paulo, Brazil Client Based (50% of the time in clients office) Syneos Health® is a leading fully-integrated life sciences services organization
At AGCO, we believe that when our employees succeed, our business succeeds. It’s a people philosophy that we believe and invest in. We make sure all our employees – in every function, every geography and at
CRA II - SR CRA Brazil Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market
Description WORK LOCATION: RIO DE JANEIRO, BRAZIL (U.S. CONSULATE) PROJECT DURATION: 18 MONTHS WITH EXPECTED FOLLOW-ON WORK WITHIN THE DoS PROGRAM Performing technical inspections of mechanical work, monitoring the contractors quality control program, and reviewing project drawings and
Desenvolver e acompanhar cronogramas e planos de projeto em parceria com times regionais no Brasil, América Latina e América do Norte; Coordenar campanhas de marketing cross-regionais, garantindo alinhamento entre áreas como branding, criação, social media, produto
Product Manager : This role is part of our Usersnap team, one of our growing brands at saas.group. This position is an interim role on a contract-basis, not a permanent employment position. Usersnap is the #1 customer feedback
The enterprise R&D digital domain forms a critical functional and data foundation as part of the end to end business transformation program across Mars Inc. It plays a pivotal role in delivering best in class digital
The enterprise R&D digital domain forms a critical functional and data foundation as part of the end to end business transformation program across Mars Inc. It plays a pivotal role in delivering best in class digital
Job Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities and close‑out visits (performed on‑site or remotely) ensuring regulatory, ICH‑GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to evaluate overall