IQVIA hiring Clinical Research Associate II

IQVIA hiring Clinical Research Associate II. BPharm, MPharm, PharmD eligible. 2+ years monitoring experience. Metro cities.

IQVIA is inviting experienced clinical research professionals to join its global clinical operations team as a Clinical Research Associate II (CRA II). This role is designed for candidates with strong onsite monitoring experience who want to work on complex, multi-center clinical trials while contributing directly to patient safety, data integrity, and regulatory compliance. The position offers exposure to large-scale studies, global sponsors, and structured career growth within one of the world’s most respected clinical research organizations.

Company Overview

IQVIA is a world leader in clinical research services, healthcare analytics, and advanced technology solutions for the life sciences industry. With operations spanning over 100 countries, IQVIA partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development and improve healthcare outcomes.

The organization is known for its deep expertise in clinical trial monitoring, regulatory compliance, real-world evidence, and data-driven decision-making. IQVIA consistently follows global standards such as ICH-GCP, FDA regulations, and international ethical guidelines, making it a preferred employer for experienced clinical research professionals seeking long-term stability and global exposure.

By integrating science, data, and technology, IQVIA plays a critical role in bringing safe and effective therapies to patients worldwide.

Job Role & Responsibilities

The Clinical Research Associate II role focuses on independent onsite monitoring and operational oversight of clinical trials. This position requires strong regulatory knowledge, excellent site management skills, and the ability to work autonomously across multiple study sites.

Key responsibilities include:

• Conducting independent onsite interim monitoring visits • Ensuring compliance with study protocols, ICH-GCP, and regulatory requirements • Performing source data verification and ensuring data accuracy • Reviewing informed consent processes and patient safety documentation • Acting as the primary point of contact for assigned clinical trial sites • Preparing, reviewing, and submitting monitoring visit reports within defined timelines • Identifying protocol deviations and supporting corrective and preventive actions • Coordinating with sponsors, project managers, and cross-functional teams • Supporting audits, inspections, and quality assurance activities

This role is ideal for professionals targeting CRA II jobs, onsite monitoring careers, and senior clinical research positions in global CRO environments.

Eligibility / Qualifications

Educational Qualifications:

BPharm, MPharm, PharmD, BHMS, BAMS, BDS

Relevant courses include: BPharm, MPharm, PharmD, BHMS, BAMS, BDS

Experience Requirements:

• Minimum 2+ years of onsite clinical trial monitoring experience
• Completion of at least 90 or more onsite interim monitoring visits
• Strong understanding of clinical trial operations and regulatory frameworks

Skill Requirements:

• In-depth knowledge of ICH-GCP and global clinical research standards
• Strong documentation and reporting skills
• Excellent communication and site management abilities
• Ability to work independently in a fast-paced clinical research environment

Location & Salary

Job Location: Metro cities across India

Employment Type: Full-time

Application Process

Eligible and interested candidates are required to apply by sending their updated CV to the IQVIA recruitment team.

Send your CV to: ashwini.veerabhadrappa@iqvia.com

Candidates should clearly mention the position title “Clinical Research Associate II” in the email subject line for accurate screening.

FAQs

Who can apply for the CRA II role at IQVIA?

Candidates with the specified qualifications and at least 2 years of onsite monitoring experience can apply.

Is onsite monitoring experience mandatory?

Yes. A minimum of 2+ years of onsite monitoring experience and 90+ interim monitoring visits is mandatory.

Is this a remote role?

No. This is an onsite role based in metro cities across India.

What career growth opportunities are available?

CRA II professionals can progress into Senior CRA, Lead CRA, or Clinical Project Management roles based on performance.

Recruitment Summary Table

Company	IQVIA
Vacancies	Clinical Research Associate II
Required Education	BPharm, MPharm, PharmD, BHMS, BAMS, BDS
Experience	2+ Years Onsite Monitoring

Tagged as: Pharma Jobs in Bangalore