Clinical Research Coordinator Job at IQVIA, Freshers & Experienced

Clinical Research Coordinator Job at IQVIA, Bangalore – Apply Now | B.Sc, B.Pharm, M.Sc | Freshers & Experienced | Clinical Trial Support

IQVIA is hiring Clinical Research Coordinators in Bangalore. Open for B.Sc, M.Sc, B.Pharm graduates with 0–3 years of experience. Work on real-world clinical trials and patient safety monitoring.

Start Your Clinical Research Career with IQVIA – Apply for CRC Role in Bangalore

Are you ready to enter the fast-growing clinical research industry? IQVIA, a global leader in healthcare intelligence and clinical trial services, is currently recruiting Clinical Research Coordinators (CRC) for its Bangalore operations. This opportunity is ideal for graduates in B.Sc, M.Sc, or B.Pharm with up to 3 years of clinical or medical experience.

Application Deadline: Apply before 14th June 2025.

If you’re passionate about patient care, research protocols, and real-world medical advancements, this is the right career move!

About IQVIA

IQVIA is a global leader in human data science and clinical research services, serving pharmaceutical, biotech, and medical device clients worldwide. IQVIA accelerates medical innovation through powerful analytics, clinical trial execution, and advanced healthcare solutions.

IQVIA offers a people-centric work culture, professional development opportunities, and a platform to contribute to real-world healthcare transformation.

Clinical Research Coordinator – Role & Responsibilities

Key Functions:

• Support investigators in planning and executing clinical research studies
• Screen, recruit, and orient study participants
• Collect and manage clinical trial data per protocol and GCP guidelines
• Coordinate patient visits, assessments, and procedures
• Prepare lab kits and handle biological sample logistics
• Perform clinical procedures like ECG, spirometry, vitals, and cannulation
• Monitor patient safety and report adverse events
• Communicate with subjects and maintain high-quality documentation
• Assist with audits, regulatory inspections, and training of site staff

Qualifications & Skills Required

Educational Background:

• Bachelor’s in Science (B.Sc), Pharmacy (B.Pharm), or Master’s in Science (M.Sc)

Experience:

• 0 to 3 years of clinical/medical experience (e.g., lab technician, medical assistant)

Essential Skills:

• Strong understanding of Good Clinical Practices (GCP)
• Familiarity with clinical trial protocols and documentation
• Skilled in Microsoft Office (Word, Excel, Outlook)
• Excellent interpersonal and communication skills
• Attention to detail and multi-tasking ability

Applicable certifications and licenses as per local regulations are required.

Why Join IQVIA?

• Exposure to cutting-edge clinical trial methodologies
• Structured on-the-job training and mentorship
• Opportunities to transition into long-term research careers
• Competitive salary and employee wellness programs

IQVIA promotes a diverse and inclusive work environment where ethical conduct, patient safety, and career growth are central values.

Apply Now

Don’t miss this chance to launch your career with one of the most respected names in global clinical research.

Apply directly at: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Clinical-Research-Co-ordinator_R1484729

Courses Applicable for This Role

B.Sc (Biology, Microbiology, Biotechnology, Chemistry, Zoology), M.Sc (Life Sciences, Biochemistry, Pharmacology), B.Pharm

Quick Summary Table