Freshers Hiring for Clinical Process Coordinator at IQVIA
Job Location: Bengaluru, Karnataka
Experience: 0–1 Year
Education: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
Mode of Application: Online
Industry: Clinical Research, Pharma Services
If you are a life science graduate or pharmacy fresher looking to build a career in the clinical research industry, IQVIA brings a golden opportunity with the role of Clinical Process Coordinator in Bangalore. This entry-level position is tailored for individuals who are passionate about working in a global pharmaceutical environment, specifically within clinical operations and trial support functions. Freshers Hiring for Clinical Process Coordinator
Let’s explore the key details, job responsibilities, required qualifications, and how you can apply for this role at one of the most reputed names in clinical research—IQVIA.
About the Company – IQVIA
IQVIA is a global leader in health information technologies, clinical research, and advanced analytics. Operating in over 100 countries, IQVIA supports pharmaceutical, biotechnology, and medical device companies by offering end-to-end solutions across the product lifecycle—from early clinical development to commercialization and real-world evidence. Freshers Hiring for Clinical Process Coordinator
IQVIA is known for driving innovation in clinical research services and is a highly respected employer in the global life sciences domain.
Official Website: www.iqvia.com
Job Title: Clinical Process Coordinator
Organization: IQVIA
Location: Bangalore, India
Employment Type: Full-Time
Work Model: Hybrid (Office-based + Work-from-Home)
Experience Level: 0–1 Year
Industry: Clinical Research/Pharma
Job Summary
As a Clinical Process Coordinator, your role will be crucial in supporting clinical trial activities by managing visit tracking, handling document reviews, and ensuring smooth coordination across teams, vendors, and systems. This role provides you with direct exposure to global clinical research practices and workflows. Freshers Hiring for Clinical Process Coordinator
It is especially ideal for freshers and early-career professionals who wish to establish a career in Clinical Trial Assistance (CTA), Clinical Research Coordination (CRC), or Regulatory Affairs.
Key Responsibilities
- CTMS Tracking: Maintain and manage clinical visit tracking in the Clinical Trial Management System (CTMS) for investigator site payments.
- Quality Checks: Perform Vendor Setup QCs, Pharmacovigilance (PV) Batch Review, and Passthrough Invoice Batch Review.
- System Access: Manage system access provisioning and revocation for team members and collaborators.
- Document Review: Assist in reviewing Authorization to Proceed (ATP) trainings and other compliance documents.
- Vendor Communication: Coordinate with translation vendors to ensure timely and accurate delivery of services.
- Compliance Monitoring: Ensure activities are carried out in compliance with clinical contracts, regulatory standards, and internal quality procedures.
- Freshers Hiring for Clinical Process Coordinator
Required Qualifications & Skills
Education:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy (B.Pharm, M.Pharm, Pharm.D), B.Sc or M.Sc in related fields.
Experience:
- 0 to 1 year of experience in clinical research, CTA, CRC, or clinical trial operations.
- Freshers with strong academic knowledge in clinical research are encouraged to apply.
Technical & Soft Skills:
- Basic understanding of clinical trial processes and regulatory documentation.
- Excellent organizational and communication skills.
- Familiarity with Microsoft Office tools (Excel, Outlook, PowerPoint).
- Ability to work independently as well as within cross-functional teams.
- Willingness to work in a hybrid model (office presence required in Bangalore).
- Freshers Hiring for Clinical Process Coordinator
Why Join IQVIA?
Global Exposure:
Work with international teams on real-time clinical studies that directly contribute to global healthcare advancements.
Learning & Development:
IQVIA invests in its employees through structured training programs, mentorship, and access to ongoing development in the field of clinical research.
Work-Life Balance:
Enjoy the flexibility of a hybrid work model, allowing better time management between professional and personal life.
Career Growth:
This entry-level role opens doors to long-term career paths in clinical operations, data management, pharmacovigilance, and regulatory affairs.
Company Reputation:
IQVIA is consistently ranked among the top employers in the life sciences industry and has a Glassdoor rating of 3.8/5.
How to Apply for Clinical Process Coordinator at IQVIA
Interested candidates can apply through IQVIA’s official job portal or leading pharmaceutical job platforms. Freshers Hiring for Clinical Process Coordinator
Steps to Apply:
- Prepare an updated CV highlighting academic credentials and any relevant internship or project experience in clinical or pharma fields.
- Visit IQVIA’s official career page or verified job listing platforms.
- Submit your application online through the job portal.
Make sure to use a clear subject line and accurate contact information. Mention any research work, coursework, or certifications related to clinical trials to boost your profile. Freshers Hiring for Clinical Process Coordinator
Recommended for:
- Fresh B.Pharm/M.Pharm/Pharm.D graduates
- B.Sc / M.Sc students in Biotechnology, Life Sciences, Microbiology, Biochemistry
- Entry-level professionals with 6–12 months’ experience in Clinical Research, CTA, CRC
Conclusion
The Clinical Process Coordinator job at IQVIA is a promising opportunity for freshers and young professionals aiming to enter the ever-growing clinical research industry. With hands-on learning, exposure to international clinical trials, and a dynamic work environment, this role is an excellent starting point for a long and impactful career. Freshers Hiring for Clinical Process Coordinator
If you meet the eligibility criteria and are passionate about healthcare innovation, don’t miss this chance—apply online today and take your first step into the clinical research domain.
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