Companhia

Bristol-Myers Squibb CompanyVer mais

addressEndereçoSão Paulo, SP
type Forma de trabalhoFull Time
CategoriaInformática

Descrição do trabalho

Job Description

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t 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. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

A BMS acredita que ter uma equipe diversificada de funcionários e uma cultura de inclusão é vital para a inovação e para executar de forma bem-sucedida nossa estratégia de negócios BioPharma.  Todas as nossas oportunidades são abertas para pessoas com deficiência (PCD), assim como para as demais dimensões no sentido mais amplo da diversidade, como gênero, idade, etnia, raça, orientação sexual & identidades, habilidades físicas, aparência, religião, origem socioeconômica, estilos de pensamento e experiências de vida.

Senior Patient Safety Associate will be responsible for performing local market core pharmacovigilance/Patient Safety activities as:

- Risk management plans
- Implementation of PV Audit and Inspection Readiness
- Planning, processing and reporting of Aggregate Reports to HA
- Maintenance of PV Awareness and Training
- Implementation of Pharmacovigilance Agreements
- Collection, follow-up and forwarding of spontaneous, literature, solicited,
post- marketing AE cases
- Submission of single cases to local HA
- Local Market Safety Data Quality

Requirements:

•     University degree (preferably life science) or nursing qualification.

•    3-5 years’ experience of working in Pharmacovigilance or in a closely aligned field (e.g. Regulatory, Clinical, or Medical Information) within the pharmaceutical industry, medical or Regulatory environment

•    Demonstrated ability to provide quality work using strong organizational, facilitation and interpersonal skills in a cross-functional team locally, within GPVE and externally.
•    Demonstrates a good understanding of the BMS organization, in particular the Global and International/Regional Safety groups and relevant local departments e.g. Regulatory and Clinical Teams. Knows where to go to for information and how the groups interact.
•    Possess excellent interpersonal, verbal, and written communication skills.  Able to research, compile and provide safety information in a clear concise manner to the local / regional team/Patient Safety HQ and externally. Sets consistent standards for others in local PV team to follow.
•    Excellent understanding of local, regional and any other relevant legislation with regard to PV (e.g. ICH, CIOMS), as well as BMS corporate and local systems (e.g. Global Safety Database, local data bases) and procedures, in order to fulfill regulatory requirements for Pharmacovigilance.
•    Maintains an awareness of the safety profile and any emerging pharmacovigilance/Patient Safety issues with BMS products (marketed or investigational) in the local affiliate and is able to represent the local Patient Safety function on cross-functional teams, providing input on drug safety issues. With support leads cross-functional teams for Risk Management and other safety related matters.  Understands the importance of pharmacovigilance within the organization and increases recognition as a PV expert.
•    Demonstrated ability to review safety information with attention to detail and accuracy, while managing multiple tasks & prioritizing work in order to meet strict deadlines. Utilizes effective problem-solving approaches to solve PV issues. Provides support to other PV Associates as required.
•    Demonstrated ability to comply with relevant internal and external processes/guidelines/regulations.
•    Strong ability to identify, address, resolve and communicates safety issues and performs root cause analysis

#LI-hybrid

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to . Visit to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Refer code: 1405902. Bristol-Myers Squibb Company - O dia anterior - 2024-01-18 16:55

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