The global healthcare and life sciences industry is evolving faster than ever, and clinical research professionals are at the heart of this transformation. If you are an experienced Clinical Research Associate looking to elevate your career with a globally respected organization, this opportunity with IQVIA could be your perfect next move. 🌍💊
IQVIA is inviting skilled and motivated professionals to join its dynamic workforce as a Clinical Research Associate – II (CRA-II). This role offers exposure to cutting-edge clinical trials, innovative healthcare solutions, and the chance to contribute meaningfully to improving patient outcomes worldwide.
🌟 Why Choose IQVIA?
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services for the life sciences industry. Known for its strong ethical standards, commitment to quality, and innovation-driven culture, IQVIA empowers professionals to grow while making a real difference in healthcare.
By joining IQVIA, you become part of a diverse and inclusive work environment that values collaboration, continuous learning, and professional excellence. Whether you aim to deepen your technical expertise or expand into leadership roles, IQVIA provides the platform and support to help you succeed. 🧠✨
📌 Job Overview: Clinical Research Associate – II
Position: Clinical Research Associate – II
Job Location: Metro Cities (India)
Industry: Clinical Research / Clinical Operations
Employment Type: Full-time
As a CRA-II at IQVIA, you will play a crucial role in ensuring the quality, integrity, and compliance of clinical trials. This position is ideal for professionals with solid onsite monitoring experience who are ready to handle increased responsibilities and work on complex global studies.
🎓 Educational Qualifications Required
Candidates applying for this role should hold one of the following degrees:
Bachelor of Pharmacy (B.Pharm)
Master of Pharmacy (M.Pharm)
Doctor of Pharmacy (Pharm.D)
Bachelor of Homeopathic Medicine and Surgery (BHMS)
Bachelor of Ayurvedic Medicine and Surgery (BAMS)
Bachelor of Dental Surgery (BDS)
These qualifications ensure a strong scientific foundation, which is essential for effective clinical trial monitoring and regulatory compliance.
✅ Eligibility Criteria & Experience Requirements
To be considered for this role, applicants must meet the following mandatory criteria:
✔ Minimum 2+ years of onsite clinical trial monitoring experience
✔ Completion of at least 90 or more onsite interim monitoring visits
✔ Hands-on experience with investigator site management
✔ Strong understanding of ICH-GCP guidelines and regulatory requirements
This role is best suited for professionals who are already comfortable managing sites independently and are confident in handling monitoring responsibilities across multiple studies.
🧪 Key Responsibilities of a CRA-II at IQVIA
As a Clinical Research Associate – II, your responsibilities may include:
🔹 Conducting onsite and remote monitoring visits as per study requirements
🔹 Ensuring patient safety, data accuracy, and protocol compliance
🔹 Reviewing source documents and verifying clinical trial data
🔹 Training site staff on study protocols and GCP standards
🔹 Identifying, documenting, and following up on protocol deviations
🔹 Ensuring timely resolution of data queries and site issues
🔹 Collaborating with cross-functional teams such as project managers and medical monitors
🔹 Maintaining accurate and complete trial documentation
Your work will directly impact the quality and success of clinical trials, making this role both challenging and highly rewarding. 🧬📊
💼 Skills That Will Help You Succeed
While technical experience is essential, IQVIA also values professionals who bring strong soft skills to the table:
🌟 Excellent communication and interpersonal skills
🌟 Strong attention to detail and problem-solving abilities
🌟 Ability to work independently with minimal supervision
🌟 Time management and organizational skills
🌟 Willingness to travel to investigator sites as required
These skills ensure effective site relationships and smooth trial execution.
📈 Career Growth & Learning Opportunities
IQVIA is known for investing in its people. As a CRA-II, you will benefit from:
📚 Continuous learning and development programs
📈 Clear career progression paths (Senior CRA, Lead CRA, Project Management, and more)
🌐 Exposure to global clinical trials and international standards
🤝 Collaboration with experienced professionals across the healthcare ecosystem
This role is not just a job—it’s a long-term career opportunity in the clinical research industry.
💡 Why This Opportunity Matters
Clinical research professionals play a vital role in bringing new therapies to patients safely and efficiently. By joining IQVIA as a CRA-II, you contribute to meaningful research that improves lives while advancing your own professional journey.
If you have the required monitoring experience and are looking to work with a globally recognized organization, this is your chance to step into a role that offers both stability and growth. 🚀
📩 How to Apply
Ready to take the next step in your clinical research career?
📧 Send your updated CV to:
ashwini.veerabhadrappa@iqvia.com
📌 Tip: Ensure your resume clearly highlights your onsite monitoring experience and the number of monitoring visits completed.
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🌐 Final Thoughts
Opportunities like this don’t come often. IQVIA’s CRA-II role is ideal for professionals who want to work on impactful studies, grow within a global organization, and stay at the forefront of clinical research innovation. If you meet the eligibility criteria, don’t hesitate—apply today and move closer to your career goals. 🌟
