Be the one building AI-powered experiences where they matter most. At Genesys, we help organizations create better customer experiences through AI-powered experience orchestration. Our platform connects people, systems, data and AI to help organizations deliver more
Are you looking to join a company where your contributions truly matter, and where youll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being
Company Overview If you see technology as a way to smooth your path in life, our team does too: Your Path, Our Journey. We believe in technology that connects talented people who embrace diversity to create
Build a Safer World. TRM Labs provides AI-powered intelligence solutions that help public and private sector agencies investigate and disrupt crime. TRMs platforms enable investigators to trace illicit activity, build cases, and construct operating pictures of
About Darkroom Darkroom is the leading next-generation growth marketing firm engineering the brands of tomorrow. Founded in 2017, we set out to redefine what a modern agency could be, by replacing the inertia of legacy advertising
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the
Job Overview With limited guidance, responsible for remote site monitoring activities to ensure sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. May
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin us as Senior Safety Reporting Specialist – To lead and oversee the preparation of complex safety reports, ensure compliance with international pharmacovigilance regulations, and drive continuous improvement in our
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical
Legal Officer, LAC RegionJob #:req38354Organization:IFCSector:LegalGrade:GFTerm Duration: Open-Ended Staff (OPEN-OP)Recruitment Type:Local RecruitmentLocation:Sao Paulo,BrazilRequired Language(s):EnglishPreferred Language(s):Portuguese, SpanishClosing Date:9/30/2026 (MM/DD/YYYY) at 11:59pm UTC Description At the International Finance Corporation (IFC), a member of the World Bank Group (WBG), you’ll
Job Overview As a Regulatory Reporting Specialist, you will be involved in submitting safety reports to regulatory authorities. Review, assess, and process safety data and information received from various sources. Distribute reports/data to internal and external
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every
AgileEngine is an Inc. 5000 company that creates award-winning software for Fortune 500 brands and trailblazing startups across 17+ industries. We rank among the leaders in areas like application development and AI/ML, and our people-first culture
At CI&T, we help large enterprises transform the potential of AI into real business impact with AI Deployment, AI-native execution, and tech-integrated business solutions. With 30 years of experience in technological transformation, we accelerate innovation with
In-House Recruiter Type: Full-time Schedule : Monday–Friday Working Hours: 7:00 AM – 3:00 PM Pacific Time / 10:00 AM – 6:00 PM Eastern Time Work Environment: Remote About the Role Talent Global is looking for a
UI/UX Designer & Data Visualization Expert We are looking for a full-time, remote Mid UI/UX Designer & Data Visualization Expert with 4+ years of professional UI/UX design experience. The ideal candidate will have experience designing complex,
(Last day to apply: Sunday, September 13) Se anima a todos los posibles solicitantes a que se desplacen y lean la descripción completa del puesto antes de presentar su candidatura. About us Legit.Health deploys computer vision
Clinical Research Coordinator in Toledo Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo. Working Hours: 20 - 24 hours per week
Required Qualifications 3 - 5 Years experience of relevant regulatory compliance including AML/CTPF, Central Bank regulations, data privacy, etc. Bachelor or above degree in law or other relevant disciplines that benefit compliance functions. Must be articulate
We are hiring for the big player and leader in the artificial intelligence (annotation) sector. Only shortlisted candidates get advanced to the next step. The client is a global leader in providing high-quality training data and