Iqvia Hiring for Clinical Research associate 2 Role
IQVIA, a global leader in clinical research and healthcare intelligence, is hiring for the role of Clinical Research Associate II (CRA II) at its Ahmedabad location. This opportunity is suited for professionals with at least 1 year of on‑site monitoring experience and a Bachelor’s degree in Life Sciences who are looking to advance their career in clinical research and trial monitoring.
The role focuses on site monitoring activities, ensuring protocol compliance, data accuracy, and adherence to regulatory guidelines across clinical studies. Candidates will collaborate closely with investigators, site staff, and internal project teams to support high‑quality clinical trial execution.
This position offers strong exposure to global clinical trials, established monitoring practices, and long‑term career growth within a globally recognized CRO
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🏢 About IQVIA
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 provides exposure to global clinical trial standards, regulated environments, and international research projects.
📊 Role Overview
- Position: Clinical Research Associate 2
- Department: CDM
- Location: Ahmadabad, India(Home based)
- Experience: 1+ Years
- Qualification: B.Pharm
- Job Type: Full-Time
- Last Date to apply: 31 March 2026
📋 Key Responsibilities – Clinical Research associate 2
- Conduct site selection, initiation, routine monitoring, and close‑out visits in compliance with the contracted scope of work, GCP, and ICH guidelines.
- Work closely with clinical sites to implement, monitor, and track recruitment plans, ensuring alignment with study timelines and enrollment targets.
- Deliver protocol and study‑specific training to assigned sites and maintain regular communication to manage expectations and address ongoing issues.
- Assess the quality and integrity of site practices, ensuring proper protocol conduct and regulatory compliance.
- Identify and escalate quality issues as required.
- Track study milestones including regulatory submissions and approvals, recruitment and enrollment, CRF completion, data query generation and resolution.
- Support study start‑up activities when applicable.
- Ensure essential site documents are available for filing in the Trial Master File (TMF).
- Verify that the Investigator Site File (ISF) is maintained according to GCP and local regulatory requirements.
- Prepare and maintain accurate monitoring visit reports, follow‑up letters, action plans, and other required study documentation.
- Collaborate with study team members to support smooth project execution and timely issue resolution.
- Support development of site‑specific recruitment plans.
- Assist with site financial management, including tracking payments and retrieving invoices in line with local requirements and clinical trial agreements.
🎓Qualification Required
Candidates applying for this role should meet the following criteria:
- Educational Background:
- Bachelor’s degree in a scientific discipline or healthcare field is preferred
- An equivalent combination of education, training, and experience may be considered
- Experience Requirement:
- Minimum 1 year of on‑site clinical monitoring experience is mandatory
🧠Skills Needed
- Good working knowledge of:
- Good Clinical Practice (GCP)
- ICH guidelines
- Understanding of clinical trial processes and site operations
- Strong attention to detail and documentation accuracy
- Good communication and interpersonal skills
- Ability to work independently and manage multiple sites
- Willingness to travel as required for site monitoring
⭐ Role Insight
The CRA II role is a key step forward in a clinical research career. Professionals at this level take greater ownership of site oversight and contribute directly to data integrity, patient safety, and regulatory compliance. Working as a CRA II at IQVIA provides hands‑on exposure to complex trials, international sponsors, and advanced monitoring frameworks, making it an important milestone toward senior CRA and leadership roles.
🎯 Ideal Candidates
This opportunity is suitable for:
- Clinical Research Associates with 1+ year of on‑site monitoring experience
- Professionals seeking advancement in clinical trial monitoring
- Candidates with strong GCP and regulatory knowledge
- Individuals aiming to work in global CRO environments
📈 Career Opportunities
With experience and strong performance, CRA II professionals can progress into roles such as:
- Senior Clinical Research Associate (CRA III)
- Lead CRA
- Clinical Trial Manager
- Clinical Operations or Project Management roles
IQVIA supports career development through training, mentoring, and global exposure.
💰 Expected Salary
- Salary details have not been disclosed by the company and will be discussed during the interview process.
- Compensation for this role will be shared by the employer at later stages of recruitment.
💡Application Tips
- Highlight regulatory compliance and site‑management skills
- Revise GCP and ICH guideline requirements
- Be prepared to discuss on‑site monitoring experiences
- Strengthen source data verification and TMF knowledge
🔗 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 2
1. Who can apply for the CRA II role at IQVIA?
Candidates with a Bachelor’s degree in Life Sciences or a healthcare discipline and at least 1 year of on‑site clinical monitoring experience.
2. What type of experience is required for this role?
Minimum 1 year of hands‑on on‑site monitoring experience, including activities such as site initiation, routine monitoring, and close‑out visits.
3. Is prior regulatory knowledge required?
Yes. A good working understanding of ICH‑GCP guidelines and global clinical research regulations is expected.
4. What will my main responsibilities be?
You will conduct site monitoring visits, ensure protocol and regulatory compliance, manage site documentation (TMF/ISF), support recruitment, and collaborate with study teams.
5. Will I work with investigators and site staff?
Yes. The role involves regular interaction with investigators, study coordinators, and site staff, including training and issue resolution.
