Portuguese (Brazil) Bilingual Audio Specialist (Freelance - Remote)
WelocalizeSalary not specified
Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Life Sciences, HealthcareIndustries
Requirements
- Bachelor’s degree in life sciences or a related field (graduated)
- Advanced level of English and Portuguese (mandatory, will be evaluated)
- 1+ year of previous experience in clinical research
- Fluency in English, Spanish, and Portuguese (trilingual role)
Responsibilities
- Process safety data according to applicable regulations, guidelines, SOPs, and project requirements
- Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information, determining initial/update status of incoming events, database entry, coding AEs and products, writing narratives, and literature-related activities
- Ensure compliance with quality, productivity, and delivery standards per project requirements
- Review, assess, and process safety data and information across service lines, received from various sources
- Distribute reports/data to both internal and external third parties following applicable regulations, Standard Operating Procedures (SOPs), and internal guidelines under the guidance and support of senior operation team members
- Liaise with different functional team members and healthcare professionals to address project-related issues
- Mentor new team members and support department initiatives as assigned by the manager
Skills
Key technologies and capabilities for this role
Questions & Answers
Common questions about this position
Is this a remote position?
Yes, this is a home-based role.
What language skills are required for this role?
Fluency in English and Portuguese at an advanced level is mandatory and will be evaluated; Spanish is also required as this is a trilingual role.
What qualifications and experience are needed for the Pharmacovigilance Specialist position?
A Bachelor’s degree in life sciences or a related field is required, along with 1+ year of previous experience in clinical research.
What is the salary or compensation for this role?
This information is not specified in the job description.
What are the main responsibilities of this position?
Main responsibilities include processing safety data, performing pharmacovigilance activities like collecting and tracking Adverse Events, ensuring compliance with standards, liaising with teams and professionals, and mentoring new members.
IQVIA
Advanced analytics and clinical research services
About IQVIA
IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.
Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees
