IQVIA is a globally recognized provider of clinical research services, commercial insights, and healthcare intelligence. With a strong presence in the life sciences and healthcare industries, IQVIA is dedicated to accelerating the development and commercialization of innovative medical treatments. The company’s mission is to improve patient outcomes and population health worldwide by creating intelligent connections and leveraging advanced data analytics.
Responsibilities in Job
As a Safety Associate Trainee at IQVIA, you will play a crucial role in processing and assessing safety data. Your key responsibilities include:
- Reviewing, assessing, and processing safety data across various service lines.
- Ensuring compliance with applicable regulations, SOPs, and internal guidelines.
- Performing pharmacovigilance activities, including tracking adverse events (AE) and endpoint information.
- Determining initial/update status of incoming events and database entry.
- Coding AE and products, writing narratives, and conducting literature-related activities.
- Meeting expected productivity and quality standards.
- Identifying quality issues and reporting them to senior team members.
- Attending project team meetings and providing feedback on challenges and successes.
- Ensuring 100% compliance with people practices and company policies.
- Performing additional duties as assigned by the operations team or management.
Qualifications
To qualify for the Safety Associate Trainee position at IQVIA, candidates should meet the following requirements:
- A Bachelor’s degree in a scientific or healthcare discipline or allied life sciences.
- Strong knowledge of medical terminology.
- Experience in pharmacovigilance or related fields (preferred but not mandatory).
- High school diploma or equivalent (for candidates with relevant experience).
Skills Required
IQVIA seeks candidates with the following skills and competencies:
- Excellent verbal and written communication skills.
- Strong attention to detail and accuracy.
- Proficiency in Microsoft Office and web-based applications.
- Ability to work independently and as part of a team.
- Time management skills and ability to meet deadlines.
- Willingness to learn and adapt to new skills in pharmacovigilance.
- Flexibility to operate in shifts and occasional travel requirements.
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