Portuguese Translator, Pharmacovigilance
at IQVIA
Desde casa, Río Negro, Argentina -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 02 Jan, 2025 | Not Specified | 04 Oct, 2024 | 1 year(s) or above | Life Sciences | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
JOB OVERVIEW
We are looking for a detail-oriented professional fluent in Spanish, English, and Portuguese to review, assess, and process safety data. You will distribute reports/data to internal and external parties, following regulations, SOPs, and internal guidelines with support from senior team members.
QUALIFICATIONS
- Bachelor’s degree in life sciences
- Up to 1 year of pharmacovigilance experience is a plus
Responsibilities:
- Complete assigned trainings on time.
- Process safety data per regulations, guidelines, SOPs, and project requirements.
- Perform pharmacovigilance activities, including collecting and tracking Adverse Events (AE), database entry, coding AE and products, writing narratives, and literature-related tasks.
- Ensure quality and productivity standards are met.
- Comply with all project-related processes and activities.
- Read and acknowledge necessary SOPs and ensure timely execution and documentation of required training.
- Create, maintain, and track cases as per project plan.
- Identify and report quality issues to senior team members.
- Demonstrate problem-solving skills.
- Liaise with functional team members and healthcare professionals to address project issues.
- Mentor new team members if assigned.
- Attend project meetings and provide feedback.
- Perform other duties as assigned.
- Lead/support department initiatives.
- Ensure compliance with all people practices and processes.
- Perform medical review of non-serious AEs and ADRs, ensuring data accuracy and completeness.
REQUIREMENT SUMMARY
Min:1.0Max:6.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Life sciences
Proficient
1
Desde casa, Argentina