IQVIA Hiring Operations Specialist 1 | pharmacovigilance & clinical safety

IQVIA Operations Specialist 1 – Life Sciences Graduate, Thāne

 Apply for IQVIA Operations Specialist 1 in Thāne. Life Sciences/Bachelor grads eligible. Full-time, office-based role in pharmacovigilance & clinical safety.

Kickstart your career in clinical research and pharmacovigilance with IQVIA in Thāne. This full-time, office-based role as an Operations Specialist 1 offers Life Sciences graduates the chance to work on safety data processing, adverse event reporting, and medical review while collaborating with global teams to ensure patient safety and regulatory compliance.

Company Overview

IQVIA is a world-leading provider of clinical research services, healthcare intelligence, and commercial insights. With a mission to accelerate the development and commercialization of innovative medical treatments, IQVIA leverages advanced technology and data analytics to improve patient outcomes globally. The company fosters a collaborative and dynamic work environment, making it a preferred destination for professionals in life sciences and healthcare.

Job Role & Responsibilities

As an Operations Specialist 1, you will:

• Process safety data and information across service lines according to SOPs and regulatory guidelines.

• Handle pharmacovigilance activities including collection, tracking, and status updates of adverse events (AEs) and adverse drug reactions (ADRs).

• Enter data into safety databases, code AEs and products, and prepare narratives.

• Support literature-related activities per project timelines.

• Ensure adherence to quality, productivity, and delivery standards.

• Read, acknowledge, and execute training per IQVIA SOPs and client SOPs.

• Liaise with cross-functional teams, including project management, clinical, data management, healthcare professionals, and clients.

• Mentor new team members when assigned.

• Participate in meetings, provide feedback, and identify quality issues for resolution.

• Lead or support department initiatives while maintaining compliance with all organizational policies.

• Perform medical review of non-serious AEs/ADRs when required, ensuring data completeness and regulatory compliance.

Eligibility / Qualifications

• High School Diploma or equivalent in scientific or healthcare disciplines (required).

• Bachelor’s degree in life sciences or related field with up to 3 years of experience, including up to 1 year in pharmacovigilance (required).

• Knowledge of medical terminology, safety databases, and applicable clinical research regulations (intermediate).

• Strong organizational, time management, and communication skills.

• Proficient in Microsoft Office and web-based applications.

• Self-motivated, flexible, and capable of working independently.

• Ability to multitask, manage deadlines, and adapt to changing priorities.

• Willingness to learn across safety service lines and work flexible shifts if required.

Relevant Courses:

B.Sc., B.Pharm, B.Tech (Life Sciences), Biotechnology, Biomedical Science, Nursing, Pharmacy, Healthcare Management

Location & Salary

• Location: Thāne, India

• Work Type: Full-time, Office-based

• Additional Locations: Available (if applicable)

• Salary: Not specified

Application Process

Apply directly via IQVIA’s careers portal: Apply Here. Apply promptly to secure your spot in this impactful role!

Why Join IQVIA?

• Opportunity to contribute to patient safety through pharmacovigilance and clinical research.

• Hands-on experience with global safety data processes and regulatory compliance.

• Exposure to cross-functional teams and mentorship from industry experts.

• Career growth opportunities in life sciences, pharmacovigilance, and healthcare intelligence.

FAQs

Q1: Who is eligible for this role?
A1: Bachelor’s degree holders in Life Sciences or related fields with up to 3 years of relevant experience, including pharmacovigilance experience.

Q2: What is the work type and location?
A2: Full-time, office-based in Thāne, India.

Q3: What skills are required?
A3: Medical terminology, database management, Microsoft Office, attention to detail, communication, multitasking, and regulatory knowledge.

Q4: Is training provided?
A4: Yes, mandatory and project-specific training is provided to ensure compliance and efficiency.

Q5: Can this role involve mentoring or leading initiatives?
A5: Yes, mentoring new team members and supporting department initiatives are part of the responsibilities.

CTA: Apply today to join IQVIA as an Operations Specialist 1 in Thāne and advance your career in pharmacovigilance and clinical research. Limited openings available—secure your future now!

---

Vertical Summary Table

Tagged as: Pharma Jobs in Bangalore