Are you looking for a rewarding career in the life sciences and healthcare industry? IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the position of Operations Specialist 1 – Lifecycle Safety in Kolkata, West Bengal. This is a full-time role with an end date of 23rd March 2025. If you have a background in life sciences, pharmacovigilance experience, and a passion for improving patient outcomes, this could be the perfect opportunity for you. Read on to learn more about the job description, qualifications, and how to apply.
Job Overview
As an Operations Specialist 1 – Lifecycle Safety, you will play a critical role in reviewing, assessing, and processing safety data and information. You will work across various service lines, ensuring compliance with regulatory standards, Standard Operating Procedures (SOPs), and internal guidelines. This role involves collaborating with internal teams, healthcare professionals, and clients to ensure the accuracy and completeness of safety data.
Key Responsibilities
- Process Safety Data: Review and process safety information in compliance with applicable regulations, guidelines, and project requirements.
- Pharmacovigilance Activities: Perform tasks such as collecting and tracking adverse events (AEs), determining initial/update status, database entry, coding AEs and products, and writing narratives.
- Quality Assurance: Ensure all deliverables meet quality standards and project timelines.
- Training Compliance: Complete assigned trainings on time and maintain up-to-date knowledge of SOPs and regulatory requirements.
- Team Collaboration: Liaise with project management, clinical teams, and healthcare professionals to address project-related issues.
- Mentorship: Guide and mentor new team members as assigned by the manager.
- Medical Review: Perform medical reviews of non-serious AEs and adverse drug reactions (ADRs) as per project requirements.
- Department Initiatives: Support or lead department initiatives to improve processes and outcomes.
Qualifications
To be considered for this role, you should meet the following criteria:
- Education:
- High School Diploma or equivalent in a scientific or healthcare discipline.
- Bachelor’s degree in life sciences or a related field is preferred.
- Experience:
- Up to 3 years of relevant experience, including up to 1 year of pharmacovigilance experience.
- Skills:
- Strong knowledge of medical terminology and safety databases.
- Proficiency in Microsoft Office and web-based applications.
- Excellent attention to detail, organizational skills, and time management.
- Strong verbal and written communication skills.
- Ability to work independently and as part of a team.
- Other Requirements:
- Flexibility to work in shifts and occasional travel.
- Commitment to IQVIA’s core values and quality standards.
About IQVIA
IQVIA is a global leader in providing advanced analytics, technology solutions, and contract research services to the life sciences and healthcare industries. With a mission to accelerate the development and commercialization of innovative medical treatments, IQVIA is dedicated to improving patient outcomes and population health worldwide.
Why Join IQVIA?
- Be part of a globally recognized organization with a strong commitment to innovation and excellence.
- Work in a collaborative and supportive environment that values diversity and inclusion.
- Gain exposure to cutting-edge technologies and processes in the life sciences industry.
- Contribute to meaningful work that impacts patient health and well-being.
