If you are looking for a rewarding career in the healthcare industry with a global leader, IQVIA is offering an exciting opportunity as an Operations Specialist 1 in Lifecycle Safety at their Mukundapur, West Bengal location. This full-time position is perfect for individuals with experience in Pharmacovigilance, a passion for medical safety, and a desire to contribute to innovative healthcare solutions. Here’s an in-depth look at the role, responsibilities, qualifications, and how to apply.
Company Introduction
IQVIA is a global leader in clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. Known for creating intelligent connections that accelerate the development of medical treatments, IQVIA plays a crucial role in improving patient outcomes and advancing population health worldwide. With a strong commitment to innovation, IQVIA helps pharmaceutical, biotech, and medical device companies navigate the complex regulatory and safety landscapes.
Job Responsibilities
As an Operations Specialist 1 in Lifecycle Safety, your primary focus will be managing and processing safety data. This includes reviewing, assessing, and distributing safety information according to global regulations and standard operating procedures (SOPs). Your responsibilities will include:
- Processing adverse event (AE) and endpoint information.
- Ensuring database entries are accurate and compliant.
- Writing narratives, coding AEs, and managing products in line with project timelines.
- Maintaining case tracking, ensuring high-quality data, and meeting productivity standards.
- Collaborating with project management, clinical teams, and healthcare professionals to address safety-related issues.
- Training and mentoring new team members and providing feedback on challenges and successes.
You will also be responsible for adhering to both IQVIA’s and client-specific SOPs, ensuring all safety activities comply with regulatory guidelines and timelines.
Qualification and Experience Requirements
The ideal candidate for this role should possess the following qualifications and experience:
- Education: Bachelor’s degree in life sciences or a related field.
- Experience: 3-5 years of relevant Pharmacovigilance experience.
- Knowledge: Strong understanding of medical terminology, pharmacovigilance concepts, and global regulatory requirements.
- Technology Skills: Proficiency in Microsoft Office and web-based applications, along with experience in safety databases and client applications.
Skills and Competencies
The role requires a well-rounded skill set that includes:
- Attention to Detail: Ensuring accuracy in processing safety data.
- Communication: Excellent verbal and written communication skills.
- Time Management: Ability to manage multiple tasks, meet deadlines, and adapt to changing demands.
- Team Collaboration: Ability to work well in a team and contribute to achieving team goals.
- Flexibility: Willingness to work in shifts and adapt to project needs.
- Problem Solving: Ability to identify and address quality issues and suggest solutions.
Additionally, candidates should demonstrate IQVIA’s core values in their daily tasks, ensuring a high standard of quality in deliverables.
