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Safety Associate Specialist With English And Turkish Language

0-2 years
Not Disclosed
10 July 16, 2025
Job Description
Job Type: Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Safety Associate Specialist (English & Turkish) – Istanbul | IQVIA

Job Summary:
IQVIA is seeking an enthusiastic and detail-oriented Safety Associate Specialist fluent in English and Turkish to join our Safety Operations team in Istanbul. This entry-level opportunity is ideal for recent Life Science graduates passionate about pharmacovigilance, drug safety, and healthcare innovation. As part of a global CRO, you'll contribute to vital safety reporting activities that directly impact patient outcomes.


Key Responsibilities:

  • Conduct pharmacovigilance activities as per project-specific requirements

  • Collect and track Adverse Events (AEs) and endpoint information

  • Review and interpret medical reports and process safety data

  • Determine initial/update status of incoming events

  • Code Adverse Events and Products, write safety narratives

  • Perform literature screening and data entry

  • Maintain high quality, productivity, and compliance standards

  • Identify and escalate quality issues to senior team members

  • Attend project meetings and report updates or challenges


Required Skills & Qualifications:

  • Bachelor’s degree in Life Sciences or a healthcare-related discipline

  • Proficiency in English (C1 or above) and Turkish (mandatory)

  • Excellent attention to detail and accuracy in documentation

  • Strong organizational and time-management skills

  • Ability to multitask and manage competing deadlines

  • Aptitude to learn new pharmacovigilance service lines and tools

  • Team player with strong interpersonal communication skills


Perks & Benefits:

  • Global exposure in a leading CRO

  • Professional development opportunities in pharmacovigilance

  • Supportive team environment and ongoing learning

  • Flexible, inclusive, and innovation-driven workplace

  • Opportunity to contribute to meaningful, life-changing healthcare outcomes


Company Description:

IQVIA is a global leader in clinical research, pharmacovigilance, and healthcare analytics, empowering life sciences organizations to improve patient outcomes through data-driven innovation. With operations in over 100 countries, IQVIA drives advancements in drug safety and healthcare delivery.


Work Mode: On-site (Istanbul)


Ready to Start Your Career in Pharmacovigilance?

Apply now to join IQVIA’s Safety Operations team and contribute to global drug safety while building a rewarding healthcare career.

Apply Today through IQVIA Careers or submit your application directly via their website.