
Senior Drug Safety Associate
1 dia atrás
With our patients at the center of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
As a **Senior Drug Safety Associate** at ICON, you'll work within a large-scale, fast-paced environment. As part of our Safety Reporting Group in ICON, our DSA's contribute to our culture of process improvement, perform expedited and periodic safety reporting, maintain projects and liaise with Sponsors, ICON project managers and investigational sites as required. We pride ourselves on our amazing company culture, where we work as one team to achieve industry-leading results.
**The role**:
- As a Snr DSA, you will be expected to prepare regulatory documentation packets and coordinate the timely completion and submission of required reports to Health Authorities, Ethic Committees, Principal Investigators and business partners.
- Ensure compliance with regulatory reporting requirements for safety reporting in clinical trials.
- Ensure all ICON, Sponsor, and regulatory timeframes are met for the reporting of safety information.
- Ensure the completion of all departmental project activities accurately in accordance with ICON standards, regulatory requirements, and contractual obligations to sponsors
**What you need**
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
-
Senior Drug Safety Associate
1 dia atrás
São Paulo, São Paulo, Brasil ICON Tempo inteiro**Senior Drug Safety Associate****JR ****Site: São Paulo -** **Brazil**At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us...
-
Senior Drug Safety Associate
Há 7 dias
São Paulo, São Paulo, Brasil Icon plc Tempo inteiroSenior Drug Safety AssociateJR Site: Regional MexicoICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.With our patients at the center of all...
-
Pharmaceutical Drug Safety Professional
Há 2 dias
São Paulo, São Paulo, Brasil beBeeExpert Tempo inteiro R$117.000 - R$147.000Drug Safety Monitoring SpecialistPfizer Worldwide Medical and Safety colleagues play a key role in connecting evidenced based, medical decision support with colleagues and stakeholders to enable better health and treatment outcomes.This includes monitoring drug, biologics and medical devices surveillance programs through intake, evaluation and processing of...
-
Drug Safety Associate
3 semanas atrás
São Paulo, São Paulo, Brasil ICON Tempo inteiroICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.With our patients at the center of all that we do, we help to accelerate the development...
-
Pharmacovigilance (Associate & Senior Associate)
3 semanas atrás
São Paulo, São Paulo, Brasil ICON Plc Tempo inteiroPharmacovigilance (Associate & Senior Assocaite) - BRAZILICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking a Pharmacovigilance...
-
Global Drug Safety Specialist
2 semanas atrás
São Paulo, São Paulo, Brasil beBeeRegulatory Tempo inteiro R$54.000 - R$78.000Pharmacovigilance Role OverviewAt the forefront of clinical development, our organization seeks a highly skilled Pharmacovigilance Assistant II to oversee the collection, processing, and timely reporting of adverse event reports. This role plays a vital part in ensuring regulatory compliance and data accuracy.Key Responsibilities:Collect, process, and report...
-
Drug Safety Specialist
1 semana atrás
São Paulo, São Paulo, Brasil beBeeCompliance Tempo inteiro R$42.000 - R$66.000Pharmacovigilance Compliance CoordinatorWe are seeking a highly motivated and detail-oriented professional to support our Pharmacovigilance Quality Team (PV-QA) with operational and compliance activities. This entry-level position offers a great foundation for individuals seeking to build a career in drug safety, quality assurance, and regulatory...
-
Senior Medical Regulatory Specialist
1 dia atrás
São Paulo, São Paulo, Brasil beBeeRegulatory Tempo inteiro R$72.951 - R$86.142Job DescriptionWe are seeking a highly skilled and experienced Senior Drug Safety Associate to join our team. The ideal candidate will have a strong background in medical sciences and excellent communication skills.The successful candidate will be responsible for preparing regulatory documentation packets and coordinating the timely completion and submission...
-
Senior Pharmacovigilance Expert
2 semanas atrás
São Paulo, São Paulo, Brasil beBeePharmacovigilance Tempo inteiro R$60.000 - R$90.000Our organization is seeking a skilled professional to fill the role of Senior Pharmacovigilance Reporting Associate. This position requires extensive experience in pharmacovigilance or drug safety reporting, as well as a strong understanding of relevant regulations and guidelines.This individual will be responsible for ensuring accurate and timely reporting...
-
Safety Assistant
2 semanas atrás
São Paulo, São Paulo, Brasil Icon Tempo inteiro**Safety Assistant****JR105807****Site: São Paulo -** **Brazil**At ICON, it's our people that set us apart.Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as...