Associate II, Pharmacovigilance - Brazil - Remote

worldwide.com; Brasília; Teletrabalho; BRL 167 400 - 223 200; Tempo integral

Resumo da oferta

A global clinical research organization is seeking an Associate II in Pharmacovigilance for a remote role based in Brasília, Brazil. This position requires at least 3 years of experience in pharmacovigilance and a bachelor's degree in a science-related field. The candidate will be responsible for managing and reporting Serious Adverse Event (SAE) data, ensuring compliance with regulatory guidelines and quality standards. Strong organizational skills, attention to detail, and proficiency in MS Office applications are essential for success in this position. Fluent English communication skills are also required.

Qualificações

• Minimum of 3 years of pharmacovigilance experience in clinical trials.
• Strong understanding of reporting requirements and international regulations.
• Ability for potential limited domestic and international travel.

Responsabilidades

• Responsible for collection and reporting of Serious Adverse Event (SAE) data.
• Author Safety Management Plan for assigned studies.
• Review incoming SAE data for completeness and accuracy.

Conhecimentos

Strong understanding of medical and scientific terminology

Excellent organizational skills

Computer literacy and MS Office proficiency

Excellent written and verbal communication skills

Ability to handle multiple competing priorities

Formação académica

Bachelor’s degree in science related field or nursing

Ferramentas

MS Office (Excel, PowerPoint, Word)

Descrição da oferta de emprego

Associate II, Pharmacovigilance - Brazil - Remote page is loaded## Associate II, Pharmacovigilance - Brazil - Remoteremote type: Remotelocations: Brasilia, Braziltime type: Full timeposted on: Posted Todayjob requisition id: JR101657**Who we are**We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.**Why Worldwide**We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!**What the Associate II, Pharmacovigilance does at Worldwide**Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions. Serves as Lead PV Associate on moderate to large sized studies that are moderate to complex in scope of work with moderate support from senior staff.**What you will do*** Author Safety Management Plan for assigned studies* Attend and present at Investigator Meetings* Review incoming SAE data for completeness and accuracy* Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information* Perform QC of SAEs processed by other PV Associates* Generate regulatory reports and perform safety submissions as needed**What you will bring to the role*** Strong understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements* Strong understanding of computer technology, and management of relational database systems, including extraction of data* Excellent organizational skills and ability to handle multiple competing priorities within tight timelines* Consistently demonstrates commitment, dependability, cooperation, adaptability and flexibility in executing daily tasks and responsibilities**Your experience*** Minimum of 3 years of pharmacovigilance experience (pre-approval clinical trials)* Bachelor’s degree in science related field, nursing or equivalent combination of relevant education and experience* Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)* Excellent written and verbal communication skills* Excellent organization skills and attention to detail* Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines* Ability to work independently, prioritize work effectively and work successfully in matrix team environment* Ability and willingness for potential limited travel (domestic and international) as needed (attend Investigator Meeting, project kick-off meeting and/or bid defense meeting)* Fluent in written and verbal EnglishWe love knowing that someone is going to have a better life because of the work we do.To view our other roles, check out our careers page at ! For more information on Worldwide, visit or connect with us on .Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law**.**