Regulatory Scientist - Hybrid ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
About CTI 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
Investigations Diligence & Compliance (Specialist) - Intern In a world of disruption and increasingly complex business challenges, our professionals bring truth into focus with the Kroll Lens. Our sharp analytical skills, paired with the latest technology,
Obrigado pelo seu interesse em trabalhar para nossa Empresa. Recrutar o talento certo é crucial para os nossos objetivos. No dia 01 de Abril de 2024, a 3M Healthcare passou por uma cisão corporativa que levou
Job Description Job Title: Medical Reviewer Employment Type: Contract Location: Brazil Experience – 2 to 5 Years About ClinChoice ClinChoice is a partner to the largest pharmaceutical, medical device, and consumer care innovators in the world.
This position is responsible for selling CTI clinical trial and regulatory and scientific affairs consulting services, including Phase I-III clinical trials and regulatory consulting services spanning pre-IND to NDA support offerings. As part of this role you
The Regulatory Services team plays a critical role in supporting UL Solutions conformity assessment activities across multiple industries and regulatory frameworks. The team works closely with regulators, certification bodies, industry associations, quality teams, and operational stakeholders
Mexico. Remote. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at
Medical Director - Cardiology & Obesity (FSP -Sponsor Dedicated) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation,
Job Description Are you passionate about clinical research and eager to make a significant impact in the healthcare industry? We are looking for a dedicated Clinical Research Associate II to join our team. In this role,
Study Start Up Associate II (Supporting North America region - US/CAN) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a
Description Medical Affairs Assistant Primary Location Latin America Brazil São Paulo Description Kenvue is looking for a MEDICAL AFFAIRS Assistant (Essential Health) The Medical Affairs Assistant, will collaborate in the following activities, for Essential Health topics: - Coordinates scientific
The Junior Associate assists in the assembling of submissions (low complexity post-approval changes in CTD or non-CTD format such as leaflet and packaging notification, administrative changes, renewals, support with Annual Reports activities, support with CMC changes
Minimum qualifications : - Bachelors degree or equivalent practical experience. - 10 years of experience working on technology policy issues within government, think tanks, public interest groups, law, or relevant industry associations. - 10 years of
Company : Qualcomm Serviços de Telecomunicações Ltda. Job Area : Legal Group, Legal Group Government Affairs General Summary : Qualcomm Government Affairs, support for the whole Latin America GA strategy conception, administration, and implementation. : - Government continuous
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description : The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role
Work Schedule Standard (Mon-Fri) Environmental Conditions Office The North American Regulatory Affairs Lead (RAL) provides innovative regulatory solutions and expertise to support product development from preclinical stages through registration and product optimization. This role involves strategic intelligence
Prepare documentation for regulatory processes to be submitted to regulatory authorities; - Handle the renewal of product and establishment licenses with relevant authorities (MAPA, Anvisa, professional councils, among others), ensuring the submission of processes within legal
Affairs Manager Position Available Patient Assistance Programs (PTA, CUP, EAP) We are seeking a Regulatory Affairs Manager to lead the management of Patient Assistance Programs (PTA, CUP, and EAP) based in Sao Paulo/Brazil. This professional will play a
Working with Us Challenging. Meaningful. Life-changing. Those arent words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department.