Manager, Pharmacovigilance
3 semanas atrás
Manager, Pharmacovigilance (Sao Paolo, Brazil)
ICON 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 development.
We are currently seeking a Manager, Pharmacovigilance to join our diverse and dynamic team. As a Manager, Pharmacovigilance at ICON, you will be responsible for overseeing the pharmacovigilance activities, ensuring the safety and efficacy of clinical trial products throughout their lifecycle. Your role will involve managing a dedicated team, ensuring compliance with regulatory requirements, and fostering a culture of safety and quality within the organization.
What You Will Be Doing:
- Leading the pharmacovigilance team in the collection, evaluation, and reporting of adverse events, ensuring compliance with regulatory guidelines and internal standards.
- Developing and implementing pharmacovigilance processes and policies to enhance the efficiency and effectiveness of safety monitoring activities.
- Collaborating with clinical, regulatory, and quality assurance teams to ensure comprehensive safety assessments and timely reporting of safety data.
- Providing training and guidance to team members and stakeholders on pharmacovigilance regulations, practices, and procedures.
- Monitoring and analyzing safety data trends, preparing risk assessments, and presenting findings to relevant stakeholders.
- Ensuring that all pharmacovigilance activities are conducted in accordance with global regulatory requirements and internal quality standards.
Your Profile:
- Bachelor’s degree in life sciences, pharmacy, or a related field is preferred, with extensive experience in pharmacovigilance or drug safety management.
- Proven experience in managing pharmacovigilance teams and activities, with a thorough understanding of regulatory requirements and safety reporting standards.
- Strong analytical skills, with experience in assessing safety data and preparing safety reports for regulatory submission.
- Excellent leadership and organizational skills, with the ability to manage multiple projects and deliver results in a fast-paced environment.
- Exceptional communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external stakeholders.
- Detail-oriented, proactive, and committed to maintaining the highest standards of safety and quality in pharmacovigilance operations.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work-life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site to read more about the benefits ICON offers.
At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here to apply.
#J-18808-Ljbffr-
Manager, Pharmacovigilance
3 semanas atrás
São Paulo, SP, Brasil ICON Plc Tempo inteiroManager, Pharmacovigilance (Sao Paolo, Brazil) ICON 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 development We are currently seeking a Manager,...
-
Manager, Pharmacovigilance
2 semanas atrás
São Paulo, Brasil ICON plc Tempo inteiroManager, Pharmacovigilance (Sao Paolo, Brazil) ICON 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 development. We are currently seeking a Manager,...
-
Manager, Pharmacovigilance
1 semana atrás
São Paulo, Brasil ENGINEERINGUK Tempo inteiroManager, Pharmacovigilance (Sao Paolo, Brazil) ICON 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 development. We are currently seeking a Manager,...
-
Manager, Global Pharmacovigilance Aggregate
2 meses atrás
São Paulo, SP, Brasil Kenvue Tempo inteiroDescription **Manager, Global Pharmacovigilance Aggregate Reporting** This position reports into the Associate Director, GARRM Team Lead and is based in Sao Paulo, Brazil. **Who we are** At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including...
-
Pharmacovigilance Coordinator
6 meses atrás
São Paulo, Brasil Galderma Tempo inteiroGalderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our...
-
Pharmacovigilance (Associate & Senior Associate)
2 semanas atrás
São Paulo, SP, Brasil ICON Plc Tempo inteiroPharmacovigilance (Associate & Senior Assocaite) - BRAZIL ICON 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 development We are currently seeking a...
-
Safety Reporting Manager, Global Aggregate Insights
4 semanas atrás
São Paulo, São Paulo, Brasil Kenvue Tempo inteiroAbout the RoleKenvue is a global leader in the development and manufacturing of iconic healthcare brands. We're driven by science, care deeply about our customers, and strive to deliver exceptional products that impact millions of lives daily.As a Safety Reporting Manager, Global Aggregate Insights, you'll be responsible for leading our team in delivering...
-
São Paulo, Brasil ENGINEERINGUK Tempo inteiroYou will need to login before you can apply for a job. Pharmacovigilance (Associate & Senior Associate) - BRAZIL, Hybrid modePharmacovigilance (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...
-
São Paulo, Brasil ENGINEERINGUK Tempo inteiroPharmacovigilance (Associate & Senior Associate) - BRAZIL, Hybrid modeICON 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 development. We are currently seeking a...
-
São Paulo, Brasil ICON Tempo inteiroPharmacovigilance (Associate & Senior Associate) - BRAZIL ICON 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 development. We are currently seeking a...
-
Strategic Alliance Manager, Global Healthcare
4 semanas atrás
São Paulo, São Paulo, Brasil Lilly Tempo inteiro**Unlocking Potential in Global Patient Safety and Regulatory Affairs**Lilly is seeking an exceptional leader to drive alliance partner relationships for Global Patient Safety (GPS) and Global Regulatory Affairs (GRA) operations. As a Strategic Alliance Manager, you will be responsible for leading vendor management for the GPS function.**Key...
-
Associate Director, Pharmacovigilance
4 meses atrás
São Paulo, SP, Brasil Thermo Fisher Scientific Tempo inteiro**Work Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Essential Functions and Other Job Information**: Oversees effectiveness of department operations to include safety processes, resource utilization, scope of work, budget and contractual issues. Develops processes and strategies designed to assist in meeting departmental and...
-
Operations Manager
7 meses atrás
Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiro**Summarized Purpose**: Manages the day-to-day operations of the safety program team. Supports staff members so that contracted safety services are provided in accordance with client and company policies and procedures. May interact with the client and internal groups to discuss and resolve issues impacting client operations. Trains and supervises healthcare...
-
RA Manager
Há 1 mês
são paulo, Brasil MSN Laboratories Tempo inteiroSurvey and implementation of processes, policies and procedures that guarantee compliance and continuity of Regulatory Affairs in each country.Responsible for the review, analysis and filing of new records before the regulatory entity in each country.Responsible for renewals and monitoring of health records.Responsible for responding to the requests or...
-
RA Manager
2 meses atrás
São Paulo, Brasil MSN Laboratories Tempo inteiroSurvey and implementation of processes, policies and procedures that guarantee compliance and continuity of Regulatory Affairs in each country.Responsible for the review, analysis and filing of new records before the regulatory entity in each country.Responsible for renewals and monitoring of health records.Responsible for responding to the requests or...
-
Clinical Operations Manager
7 meses atrás
Sao Paulo, Brasil MSD Tempo inteiroThis role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the Sr. COM, Head COMs or CRD, the person is responsible for...
-
Regulatory Affairs Manager
4 meses atrás
São Paulo, Brasil MSN Laboratories Tempo inteiroSurvey and implementation of processes, policies and procedures that guarantee compliance and continuity of Regulatory Affairs in each country.Responsible for the review, analysis and filing of new records before the regulatory entity in each country.Responsible for renewals and monitoring of health records.Responsible for responding to the requests or...
-
RA Manager
2 meses atrás
são paulo, Brasil MSN Laboratories Tempo inteiroSurvey and implementation of processes, policies and procedures that guarantee compliance and continuity of Regulatory Affairs in each country.Responsible for the review, analysis and filing of new records before the regulatory entity in each country.Responsible for renewals and monitoring of health records.Responsible for responding to the requests or...
-
Regulatory Affairs Manager
4 meses atrás
São Paulo, Brasil MSN Laboratories Tempo inteiroSurvey and implementation of processes, policies and procedures that guarantee compliance and continuity of Regulatory Affairs in each country.Responsible for the review, analysis and filing of new records before the regulatory entity in each country.Responsible for renewals and monitoring of health records.Responsible for responding to the requests or...
-
RA Manager
2 meses atrás
são paulo, Brasil MSN Laboratories Tempo inteiroSurvey and implementation of processes, policies and procedures that guarantee compliance and continuity of Regulatory Affairs in each country. Responsible for the review, analysis and filing of new records before the regulatory entity in each country. Responsible for renewals and monitoring of health records. Responsible for responding to the requests or...
