IQVIA Hiring Safety Associate | Pharmacovigilance Jobs

QVIA Hiring Safety Associates in Kochi | 1–3 Years Pharmacovigilance Case Processing Roles

Looking to grow your career in pharmacovigilance and drug safety? IQVIA is hiring Safety Associates in Kochi for professionals with 1–3 years of experience in PV case processing and safety data management. This is an excellent opportunity for candidates aiming to build a stable and high-growth career in global drug safety operations.

This role focuses on adverse event case processing, regulatory compliance, and safety data handling, making it ideal for professionals in pharmacovigilance, clinical safety, and healthcare analytics domains.

About IQVIA

IQVIA is a global leader in clinical research, healthcare intelligence, and data-driven solutions. We help accelerate medical innovations to improve patient outcomes worldwide.

Job Overview

Review, assess and process Safety data and information, across service lines, received from various sources and distribute reports/data onwards to both internal and external third parties following applicable regulations SOPs and internal guidelines under guidance and support of senior operation team members.

. If you have a background in Life Sciences and 1-1.5 years of experience in pharmacovigilance, this is an excellent opportunity to advance your career.

Job Responsibilities

• To Prioritize and complete the assigned training on time.
• Process Safety data according to applicable regulations, guidelines, Standard Operating procedures (SOPs) and project requirements.
• To perform Pharmacovigilance activities per project requirement, including but not limited to, collecting and tracking incoming Adverse Events(AE)/endpoint information
• determining the initial/update status of incoming events
• database entry
• Coding AE and Products, writing narratives, and doing literature-related activities as per internal/ project timelines.
• Ensure to meet quality standards per project requirements.
• Ensure that productivity and delivery standards are met per project requirements.
• To ensure compliance with all project-related processes and activities.
• Creating, maintaining and tracking cases as applicable to the project plan.
• Identify quality problems, if any, and bring them to the attention of a senior team member.
• To demonstrate problem-solving capabilities.
• Mentor new team members if assigned by the Manager.
• Attend project team meetings and provide feedback to the operations manager on any challenges/issues or successes.
• 100% compliance towards all people’s practices and processes
• Perform other duties as assigned.

Required Qualifications

• Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related field.
• Experience: 1-1.5 years in pharmacovigilance or drug safety.
• Knowledge of medical terminology and safety databases.
• Strong communication, time management, and organizational skills.
• Ability to work independently and in a team.
• Proficiency in Microsoft Office and web-based applications.
• Willingness to work in shifts and occasional travel.

Application Process

Interested candidates can apply by sending their updated resume to the email below:

Email: sherry.thammappakm@iqvia.com

Candidates are advised to apply early as safety associate roles are highly competitive.

Job Summary Table

Apply today and take your career to the next level in Pharmacovigilance with IQVIA!