Job Overview
Join IQVIA as a Safety Associate , assessing, and processing safety data and information across various service lines. This data is received from multiple sources and must be distributed to both internal and external third parties in compliance with applicable regulations, SOPs, and internal guidelines. The Safety Associate will work under the guidance and support of senior operation team members.
- Company Name: IQVIA
- Role: Safety Associate
- Experience: 1 to 1.5 years of relevant experience
- Salary: Not disclosed
- Employment Type: Full-time
- Location: Kolkata, West Bengal
Essential Functions
- Prioritize and complete assigned training on time.
- Process safety data according to regulations, guidelines, SOPs, and project requirements.
- Perform pharmacovigilance activities, including collecting and tracking Adverse Events (AE) and endpoint information, determining the initial/update status of incoming events, and entering data into the system.
- Code AE and products, write narratives, and handle literature-related activities as per internal and project timelines.
- Ensure compliance with quality standards and project delivery requirements.
- Create, maintain, and track cases as per the project plan.
- Identify and report quality issues to senior team members.
- Demonstrate problem-solving capabilities.
- Mentor new team members, if assigned by the manager.
- Attend project team meetings and provide feedback to the operations manager regarding challenges, issues, or successes.
- Ensure 100% compliance with all people practices and processes.
- Perform other duties as assigned.
Qualifications
-
Required:
- High School Diploma or equivalent in a scientific, healthcare, or allied life sciences discipline.
- A minimum of a Bachelor’s Degree in a scientific, healthcare, or allied life sciences discipline with 1 to 1.5 years of relevant experience.
Preferred Skills:
- Good knowledge of medical terminology (Intermediate level).
- Working knowledge of applicable Safety Databases (Beginner level).
- Knowledge of global, regional, and local clinical research regulatory requirements (Beginner level).
- Attention to detail and accuracy (Beginner level).
- Proficient in Microsoft Office and web-based applications (Beginner level).
- Strong organizational, time management, and communication skills (Intermediate level).
- Self-motivated and flexible (Intermediate level).
- Ability to follow instructions/guidelines, work independently, and demonstrate initiative (Intermediate level).
- Ability to multitask, manage competing priorities, and meet deadlines (Beginner level).
- Ability to delegate tasks to less experienced team members (Beginner level).
- Willingness to learn new skills across Safety service lines (Beginner level).
- Ability to establish and maintain effective relationships with coworkers, managers, and clients (Beginner level).
- Ability to work as a team player and contribute to team goals (Beginner level).
- Ensure quality of deliverables according to agreed terms (Beginner level).
- Demonstrate IQVIA core values in daily tasks (Beginner level).
- Frequent use of telephone and face-to-face communication, requiring accurate speech perception (Beginner level).
- Regular sitting for extended periods (Beginner level).
- Occasional travel may be required (Beginner level).
- Flexibility to operate in shifts (Beginner level).
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company works to accelerate the development and commercialization of innovative medical treatments, improving patient outcomes and population health worldwide.
Location
Kolkata, West Bengal
For more information about the role and to apply, please visit the official IQVIA jobs page: IQVIA Careers.
Click Here to Apply Now
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