Pharmacovigilance Coordinator - São Paulo

We are currently seeking a Supervisor, Pharmacovigilance to join our diverse and dynamic team. As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed prod ...

We aim to prevent stop and cure diseases and ensure everyone has access to healthcare today and for generations to come at Roche where every voice matters. · The Position · A healthier future drives us to innovate continuously promoting science ensuring that everyone has access t ...

Collaborate with the execution, implementation, maintenance, and oversight of the local PV (Pharmacovigilance) system Manage key safety-related activities in line with Roche procedures Act as the primary safety expert and trusted point of contact for Global Safety, PV Hubs, and l ...

+ Pharmacovigilance Supervisor - Supervise the day-to-day pharmacovigilance operations + Collaborate with cross-functional teams to optimize pharmacovigilance processes + Ensure compliance with global regulatory requirements and internal standard operating procedures for safety r ...

We are currently seeking a Pharmacovigilance Supervisor to join our diverse and dynamic team. · ...

We are seeking a Pharmacovigilance Supervisor to oversee safety monitoring and reporting of adverse events related to clinical trials and marketed products. · Supervising pharmacovigilance operations. · Collaborating with cross-functional teams. · Ensuring compliance with global ...

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, · & EAP) based in Sao Paulo/Brazil. · ...

Lilly is seeking Case Management Medical Review Scientists in Indianapolis, · USA. · Conduct comprehensive medical review of Individual Case Safety Reports (ICSRs) · Evaluate cases for potential quality issues with Lilly products affecting patient safety · Collaborate with cross- ...

We are seeking an experienced · Regulatory Affairs Lead to drive regulatory strategy and execution for the Brazilian market.This role will lead end-to-end regulatory planning, · stakeholder engagement,and submission managementto support product registration,lifecycle maintenance ...

Lilly busca un Case Management Medical Review Physician para realizar revisiones médicas exhaustivas de informes individuales de seguridad (ICSRs), garantizar la precisión e integridad de los informes regulatorios globales y colaborar con equipos transfuncionales. · ...

We are looking for a Case Management Medical Review Physician to conduct comprehensive medical review of Individual Case Safety Reports (ICSRs), ensure accuracy and integrity of global regulatory reports, and collaborate cross-functionally. · Conduct comprehensive ICSR medical re ...

+ Job Title: Medical Reviewer · + Established in 1995, we provide expertise in clinical operations, biometrics, regulatory affairs, pharmacovigilance, medical affairs and toxicology to help our partners advance healthcare by accelerating clinical trials with data-driven insights. ...

We are looking for a dedicated Clinical Research Associate to join our team.In this role, you will be the primary site contact throughout all phases of clinical research studies, ensuring compliance with regulations and contributing to the success of our clinical trials. · Develo ...

We are looking for a dedicated Clinical Research Associate III to join our team. · As a Clinical Research Associate II, you will play a crucial role in developing and maintaining strong relationships with study sites,Ensure compliance with International Council for Harmonisation/ ...

We are looking for a dedicated Clinical Research Associate to join our team. · Bachelor's degree · Solid experience as a Clinical Research Associate, preferably in a similar role. · ...

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 III to join our team. In this role, you will be the primary site contact throughout all phases of clinical rese ...

Job summary · About this Job · We are looking for highly motivated professionals with passion for medicines development who want to join our team as Global Clinical Development Manager Biosimilar Oncology. We welcome applicants with diverse backgrounds & experiences. · Clinical D ...

This position works out of our São Paulo location in the Established Pharmaceuticals Division.We are committed to bringing the benefits of our trusted medicines to more people in the world's fastest-growing countries. · ...

The position works out of our São Paulo location in the Established Pharmaceuticals Division. We are committed to bringing the benefits of our trusted medicines to more people in the world's fastest-growing countries. · Stays abreast with medical/scientific knowledge, competitor ...

We are looking for a dedicated Clinical Research Associate III to join our team. · Develop and maintain strong relationships with study sites throughout all phases of clinical trials. · Ensure compliance with International Council for Harmonisation/Good Clinical Practice (ICH-GCP ...