Job Title: Pharmacovigilance Linguist Specialist
Location: Bengaluru, India (Hybrid – 3 days in office)
About PRI Global:
PRI Global is a leading global consulting and clinical support organization dedicated to excellence in pharmacovigilance and drug safety. We are committed to providing innovative solutions and expert guidance to our clients worldwide. We are currently seeking a highly motivated and skilled Pharmacovigilance Linguist Specialist to join our growing team in Bengaluru. This role offers a unique opportunity to leverage your linguistic expertise and pharmacovigilance knowledge in a dynamic and international environment.
Job Summary:
We are seeking a talented Pharmacovigilance Linguist Specialist to contribute to our global safety operations. In this role, you will be responsible for translating, interpreting, and validating safety information in multiple languages, primarily Japanese, French, Arabic, or Persian, to support pharmacovigilance activities. You will play a vital role in ensuring the accuracy and integrity of adverse event reports and related documentation, contributing to the overall safety and efficacy of pharmaceutical products. This is a hybrid position based in Bengaluru, requiring three days of on-site work per week.
Key Responsibilities:
- Language Expertise: Translate, interpret, and validate safety information related to adverse event reports, medical literature, and other pharmacovigilance documents in Japanese, French, Arabic, or Persian.
- Case Processing Support: Assist with case intake, triage, narrative writing, and case quality review to ensure compliance with global safety standards and regulatory requirements.
- Adverse Event Reporting: Accurately interpret and process adverse event reports, ensuring all relevant information is captured and documented in a clear and concise manner.
- Collaboration: Work closely with global safety teams, medical reviewers, and other stakeholders to facilitate effective communication and information sharing.
- Documentation and Data Accuracy: Maintain high-quality documentation and ensure data accuracy across all pharmacovigilance systems.
- Compliance: Adhere to global pharmacovigilance regulations, guidelines, and standard operating procedures (SOPs).
- Quality Assurance: Participate in quality control processes to ensure the accuracy and consistency of translated and interpreted materials.
- Continuous Improvement: Identify opportunities to improve processes and workflows related to linguistic support in pharmacovigilance.
Eligibility & Qualifications:
- Experience: 2-5 years of experience in Pharmacovigilance or a related domain (e.g., clinical research, medical affairs).
- Education: A Bachelor’s degree in Pharmacy, Nursing, Medicine, Dentistry, Life Sciences, or a related field.
- Linguistic Skills: Fluency (written and verbal) in English and at least one of the following languages: Japanese, French, Arabic, or Persian. Certification in at least two languages is preferred (A1/A2/B1/B2 levels).
- Pharmacovigilance Knowledge: A solid understanding of pharmacovigilance principles, processes, and regulatory requirements.
- Communication Skills: Excellent written and verbal communication skills, with the ability to effectively communicate complex information to diverse audiences.
- Analytical Skills: Strong analytical and problem-solving skills, with the ability to critically evaluate safety information and identify potential issues.
- Attention to Detail: Meticulous attention to detail and a commitment to accuracy and quality.
- Teamwork: Ability to work effectively in a team environment and collaborate with colleagues from different cultural and professional backgrounds.
- Adaptability: Ability to adapt to changing priorities and work effectively under pressure.
- Technical Skills: Proficiency in using pharmacovigilance databases and software applications.
- Notice Period: Immediate joiners or candidates serving notice period are preferred.
Why Join PRI Global?
- Global Exposure: Gain valuable experience working with a recognized global consulting and clinical support organization.
- Hybrid Work Environment: Enjoy the flexibility of a hybrid work model with three days in the office.
- Career Growth: Opportunity for career advancement in pharmacovigilance, medical writing, and linguistic safety review.
- Multilingual Skills Utilization: Utilize and enhance your multilingual skills in a dynamic and rewarding role.
- Impactful Contribution: Make a meaningful contribution to drug safety and patient health on a global scale.
- Collaborative Culture: Be part of a supportive and collaborative team environment.
- Continuous Learning: Opportunities for continuous learning and professional development.
To Apply:
We encourage qualified candidates to apply. Please submit your resume and cover letter detailing your relevant experience and qualifications. We look forward to hearing from you!