IQVIA has announced hiring for three full-time positions in India: Safety Associate – Japanese Language in Hyderabad, Operations Specialist – 1 – Japanese in Pune, and Data Receipt Technician in Thane, Maharashtra. The openings cover pharmacovigilance, safety data processing, ECG data management, clinical trial support, and related operational activities.

Candidates with relevant scientific or healthcare qualifications can apply for the safety positions, while graduates from any field are preferred for the Data Receipt Technician role.

IQVIA Recruitment 2026 – Job Details

1. Safety Associate – Japanese Language

Location: Hyderabad, Telangana
Job Requisition ID: R1572879

Job Overview

The Safety Associate will review, assess, and process safety data received from various sources. The role involves pharmacovigilance case processing, adverse event tracking, database entry, medical coding, narrative writing, and compliance with applicable regulations and standard operating procedures (SOPs).

Key Responsibilities

• Process safety data according to applicable regulations, SOPs, guidelines, and project requirements.
• Collect and track incoming adverse event (AE) and endpoint information.
• Determine the initial or update status of incoming events.
• Perform database entry and code adverse events and products.
• Write case narratives and support literature-related activities.
• Create, maintain, and track cases according to project requirements.
• Meet project-specific quality, productivity, and delivery standards.
• Identify quality issues and escalate them to senior team members.
• Complete assigned training and comply with project processes.
• Attend project meetings and provide feedback on operational challenges.

Eligibility and Qualifications

• High school diploma or equivalent in a scientific, healthcare, or allied life sciences discipline.
• A bachelor’s degree in a scientific, healthcare, or allied life sciences discipline, with 1–1.5 years of relevant experience.

Required Skills

• Medical terminology knowledge.
• Basic working knowledge of safety databases.
• Understanding of clinical research regulatory requirements.
• Attention to detail and accuracy.
• Microsoft Office and web-based application skills.
• Strong organizational, time management, and communication skills.
• Ability to manage multiple tasks and meet deadlines.
• Flexibility to work in shifts.

2. Operations Specialist – 1 – Japanese

Location: Pune, Maharashtra
Job Requisition ID: R1556987

Job Overview

The Operations Specialist will perform pharmacovigilance and safety data processing activities, including adverse event case management, database entry, medical coding, narrative writing, and quality checks. Depending on project requirements, the role may also involve medical review of non-serious adverse events and adverse drug reactions.

Key Responsibilities

• Process safety data according to applicable regulations, SOPs, and project guidelines.
• Collect and track adverse event information and determine case status.
• Perform database entry, adverse event coding, product coding, and narrative writing.
• Create, maintain, and track safety cases.
• Ensure compliance with training requirements, project processes, and quality standards.
• Coordinate with project management, clinical, and data management teams.
• Liaise with healthcare professionals, investigators, medical monitors, and site coordinators to resolve project-related issues.
• Communicate with clients regarding day-to-day case processing activities when required.
• Identify quality issues and support corrective actions.
• Support departmental initiatives and mentor team members when assigned.
• Conduct medical review of non-serious AEs and ADRs when required, including review of coding, medical history, concomitant medications, expectedness, and causality assessment.

Eligibility and Qualifications

• Bachelor’s degree in a scientific, healthcare, or allied life sciences discipline.
• Up to 3 years of experience, or an equivalent combination of experience, training, and education.

Required Skills

• Good knowledge of medical terminology.
• Working knowledge of safety databases and internal or client applications.
• Understanding of applicable global, regional, and local clinical research regulations.
• Strong attention to detail and quality standards.
• Proficiency in Microsoft Office and web-based applications.
• Strong communication, organizational, and time management skills.
• Ability to manage competing priorities and strict deadlines.
• Teamwork, problem-solving, and adaptability.
• Flexibility to work in shifts.

3. Data Receipt Technician

Location: Thane, Maharashtra
Job Requisition ID: R1573406

Job Overview

The Data Receipt Technician will support ECG data receipt and processing for clinical studies. The role includes verifying ECG-related queries, maintaining study databases and trackers, coordinating with clinical study teams, and supporting data reconciliation and quality control.

Key Responsibilities

• Set up study details and custom IDs on data receiving servers.
• Receive ECGs and review system-generated queries.
• Verify demographic information and correct database entries according to self-evident correction guidelines.
• Raise data clarification forms (DCFs) for discrepancies and process site responses.
• Validate test ECGs and maintain related trackers.
• Enrol patients in analysis databases and create clinical trial site records.
• Coordinate site qualification activities and maintain relevant documentation.
• Allocate ECGs for analysis and track completion within study-specific turnaround times.
• Perform source data verification (SDV) and maintain study-specific logs.
• Support data reconciliation and quality control.
• Coordinate with project management, data management, and connected devices operations teams.
• Track study archival activities, document retrieval, and data destruction processes as required.
• Prepare performance metrics and share them with sponsors according to agreed requirements.
• Train and mentor junior team members.

Eligibility and Qualifications

• Graduates from any field are preferred.
• Experience working with Excel and Microsoft Office, or an equivalent combination of education, training, and certification.
• Ability to understand ECG quality.

Required Skills

• Microsoft Excel, Word, and PowerPoint.
• Data verification and attention to detail.
• Ability to maintain trackers and study records.
• Understanding of ECG data quality.
• Coordination and communication skills to work with project and data management teams.

IQVIA Recruitment 2026 – Application Details

1. Safety Associate – Japanese Language

• Location: Hyderabad, Telangana
• Experience: 1–1.5 years of relevant experience

2. Operations Specialist – 1 – Japanese

• Location: Pune, Maharashtra
• Experience: Up to 3 years

3. Data Receipt Technician

• Location: Thane, Maharashtra
• Experience: 0 – 1 Years