Are you passionate about advancing healthcare and ensuring patient safety? IQVIA, a global leader in clinical research and healthcare intelligence, is hiring a Safety Associate Trainee in Bangalore, India. This full-time role offers an exciting opportunity to kickstart your career in pharmacovigilance, working with cutting-edge medical data to support innovative treatments. If you have a background in life sciences or healthcare and thrive in a dynamic, team-oriented environment, this role is perfect for you. Explore this career opportunity and apply today through Pharmabharat.com!
Responsibilities
As a Safety Associate Trainee at IQVIA, you will play a critical role in processing and analyzing safety data to ensure compliance with regulations and project requirements. Your key responsibilities include:
- Prioritizing and completing assigned trainings to stay updated on pharmacovigilance processes.
- Processing safety data in accordance with applicable regulations, Standard Operating Procedures (SOPs), and project guidelines.
- Performing pharmacovigilance activities, such as collecting and tracking Adverse Events (AE) and endpoint information.
- Determining initial/update status of incoming events and performing accurate database entry.
- Coding Adverse Events and products, writing narratives, and conducting literature-related activities.
- Assuming workflow responsibilities as directed by senior team members or managers.
- Meeting productivity and quality standards to ensure high-quality deliverables.
- Identifying and reporting quality issues to senior team members or mentors.
- Attending project team meetings to provide feedback on challenges, successes, or issues.
- Ensuring 100% compliance with IQVIA’s people practices and processes.
- Performing additional duties as assigned to support team objectives.
Qualifications
To succeed as a Safety Associate Trainee, you should meet the following qualifications:
- Education: High School Diploma or equivalent in a scientific or healthcare discipline, or allied life sciences. A Bachelor’s Degree in a related field is preferred.
- Medical Terminology: Strong understanding of medical terminology.
- Communication Skills: Excellent verbal and written communication skills.
- Teamwork: Ability to work collaboratively and contribute to team goals.
- Technical Skills: Proficiency in Microsoft Office and web-based applications.
- Attributes: Self-motivated, flexible, detail-oriented, and accurate.
- Time Management: Ability to manage competing priorities and meet deadlines.
- Adaptability: Willingness to learn new skills across safety service lines.
- Physical Requirements: Comfort with extensive keyboard use, telephone, and face-to-face communication. Ability to sit for extended periods.
- Availability: Flexibility to work in shifts and occasional travel, if required.
Benefits of Working at IQVIA
Joining IQVIA as a Safety Associate Trainee offers numerous benefits, including:
- Career Growth: Gain hands-on experience in pharmacovigilance and access opportunities for professional development.
- Global Impact: Contribute to innovative medical treatments that improve patient outcomes worldwide.
- Supportive Environment: Work under the guidance of experienced mentors and collaborate with a dynamic team.
- Reputable Employer: Be part of IQVIA, a trusted name in clinical research and healthcare intelligence.
How to Apply
FAQs
Q: What is the role of a Safety Associate Trainee at IQVIA?
A: The Safety Associate Trainee processes safety data, tracks adverse events, performs database entry, and ensures compliance with regulations under the guidance of senior team members.
Q: Is prior pharmacovigilance experience required?
A: No prior experience is required. A background in life sciences or healthcare, along with a willingness to learn, is sufficient to qualify for this role.
