IQVIA Hiring – Clinical Research Associate I | Mumbai & Bangalore
IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the role of Clinical Research Associate I (CRA I) at its Mumbai and Bangalore locations. This opportunity is suitable for B.Pharm and M.Pharm graduates with 0–3 years of experience who are looking to start or grow their career in clinical research and site monitoring.
The role focuses on supporting clinical trial monitoring activities, ensuring protocol compliance, data accuracy, and adherence to GCP and regulatory requirements. Candidates will work closely with investigational sites and cross‑functional project teams to support high‑quality clinical trial execution.
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🏢 Company Overview
IQVIA is a global leader in clinical research services, healthcare analytics, and technology solutions. The organization supports pharmaceutical, biotechnology, and healthcare companies across the complete drug development lifecycle. Working at IQVIA offers exposure to global clinical standards, regulatory compliance frameworks, and large‑scale multinational studies.
📊 Position Details
- Position: Clinical Research Associate I
- Department: CDM
- Location: Bangalore, Mumbai
- Experience: 0- 3 years
- Qualification: B.Pharm, M.Pharm
- Job Type: Full-Time
- Last Date of application: 2 April 2026
📋 What You Will Do– Clinical Research Associate I
- Site Monitoring Activities: Conduct site selection, initiation, routine monitoring, and close‑out visits in line with the contracted scope of work and GCP / ICH guidelines.
- Subject Recruitment Support: Work closely with investigational sites to implement, track, and drive subject recruitment plans, ensuring alignment with study timelines and project requirements.
- Site Training & Communication: Deliver protocol and study‑related training to assigned sites.
- Maintain regular communication with site personnel to manage expectations and resolve ongoing study issues.
- Quality Oversight & Compliance: Evaluate the quality and integrity of site practices, ensuring proper protocol conduct and adherence to applicable regulatory requirements.
- Identify and escalate quality issues to project teams as appropriate.
- Study Progress Management: Monitor study progress by tracking regulatory submissions and approvals, recruitment and enrollment status, CRF completion, and data query generation and resolution.
- Support study start‑up activities when required.
- TMF & ISF Management: Ensure essential site documents (copies/originals as required) are available for filing in the Trial Master File (TMF).
- Verify that the Investigator Site File (ISF) is maintained in compliance with GCP, ICH, and local regulatory requirements.
- Monitoring Documentation: Create and maintain accurate monitoring visit reports, follow‑up letters, action plans, and other required site management documentation.
- Cross‑Functional Collaboration: Collaborate with study team members to support timely and effective project execution.
- Additional Study Responsibilities (If Applicable): Support the development of site‑specific subject recruitment plans.
- Assist with site financial management, including tracking payments and retrieving invoices in accordance with executed clinical trial agreements and local requirements.
🎓Who Can Apply
Candidates applying for this role should meet the following criteria:
- Educational background in Life Sciences, Pharmacy, Nursing, or related fields
- Basic understanding of clinical research and trial processes
- Willingness to travel to study sites as required
- Interest in clinical monitoring and site management activities
(Prior clinical research exposure is an advantage but not mandatory for CRA I roles.)
🧠 Key Skills
The following skills are important for success in this role:
- Knowledge of clinical trial fundamentals and GCP principles
- Strong attention to detail and documentation accuracy
- Good communication and interpersonal skills
- Ability to manage multiple tasks and timelines
- Willingness to learn site monitoring and compliance processes
⭐ Work Insight
The CRA I role is a foundational position in clinical research that trains professionals in site monitoring, regulatory compliance, and trial oversight. This role helps candidates understand how clinical trials are conducted in real‑world settings and prepares them for advanced monitoring responsibilities. Experience as a CRA I is highly valuable for long‑term careers in global clinical research.
🎯 Suitable For
This opportunity is suitable for:
- Fresh graduates aiming to start a clinical research career
- Candidates with basic clinical research training or certifications
- Coordinators or clinical professionals transitioning into monitoring roles
- Individuals interested in site‑level trial oversight
📈 Career Path
With experience and consistent performance, CRA I professionals can progress into roles such as:
- Clinical Research Associate II (CRA II)
- Senior Clinical Research Associate
- Lead CRA
- Clinical Trial Manager
IQVIA also provides structured training and mentorship programs that support career advancement.
💰 Salary Range
- Expected Salary: As per IQVIA company standards
Salary depends on experience level, location, and internal company policies.
💡 Application Tips
- Highlight communication, coordination, and documentation skills in your resume
- Revise GCP and clinical trial basics
- Understand the role of CRAs in site monitoring
- Be prepared to discuss clinical research workflows
🔗 Application Process
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer:This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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❓FAQ – Clinical Research Associate I
1. Who can apply for the CRA I role at IQVIA?
Candidates with a Bachelor’s degree in Life Sciences, Pharmacy, or a healthcare‑related discipline, along with 0–3 years of experience in clinical research or monitoring, can apply.
2. Is this role suitable for freshers?
Yes. This role is suitable for freshers or early‑career professionals, especially those who have completed CRA training or have basic clinical research exposure.
3. What are the main responsibilities of a CRA I?
You will perform site monitoring visits, support subject recruitment, ensure protocol and regulatory compliance, manage study documentation (TMF/ISF), and collaborate with study teams for smooth trial execution.
4. Is priormonitoring experience required?
Prior on‑site monitoring experience is preferred but not always mandatory. Some candidates may qualify based on CRA training programs or relevant clinical research exposure.
5. What regulatory knowledge is required for this role?
A basic understanding of ICH‑GCP guidelines and clinical research regulations is expected. Additional training is provided by IQVIA.
