The clinical research industry in India is growing rapidly, driven by advancements in healthcare, pharmaceuticals, and medical technology 🌍. With an increasing number of clinical trials being conducted across hospitals and research sites, the demand for skilled Clinical Research Professionals has never been higher.
If you are passionate about clinical research, site management, regulatory compliance, and patient-focused studies, this is an excellent opportunity to build or advance your career. IQVAMED is expanding its Clinical Research Support and Site Management team and is currently hiring for the role of Clinical Research Coordinator (CRC).
This role is ideal for professionals who enjoy working in a structured research environment, collaborating with medical teams, and contributing to high-quality clinical trials that make a real difference in patient care 💙.
🔬 Job Role: Clinical Research Coordinator (CRC)
The Clinical Research Coordinator (CRC) plays a critical role in the successful execution of clinical trials at research sites. As a CRC, you will act as a key link between investigators, sponsors, study participants, and regulatory teams.
📍 Location: Bengaluru
🏢 Work Mode: On-site
📌 Number of Vacancies: 2
This is an on-site opportunity, offering hands-on exposure to real-time clinical research activities in a professional healthcare environment.
🧠 Key Skills & Abilities Required
The ideal candidate for this role should possess a balanced mix of technical understanding and interpersonal skills. Some of the most important abilities include:
🗣️ Effective Communication Skills
Strong verbal and written communication skills are essential, as CRCs regularly interact with doctors, nurses, sponsors, and patients.
📊 Presentation & Documentation Skills
You should be comfortable preparing study-related documents, presentations, and reports in a clear and professional manner.
🤝 Ability to Work with Medical Personnel
CRCs must communicate effectively with investigators and clinical staff while maintaining professionalism and accuracy.
❤️ Passion for Clinical Research
A genuine interest in clinical research, patient safety, and ethical trial conduct is highly valued.
🗂️ Organizational & Time Management Skills
Managing multiple study tasks, timelines, and documentation requires excellent organizational abilities.
👥 Teamwork & Independent Working Ability
You should be able to collaborate within a team as well as work independently when required.
🔄 Flexibility & Adaptability
Clinical research environments can change quickly. The ability to adapt to different scenarios is an important skill for success.
🧾 Roles & Responsibilities of a Clinical Research Coordinator
While responsibilities may vary depending on the study and site, typical duties of a CRC include:
📑 Coordinating day-to-day clinical trial activities
🧾 Maintaining accurate study documentation and records
🔍 Ensuring compliance with study protocols and regulatory guidelines
👩⚕️ Supporting investigators during trial execution
🧑🤝🧑 Assisting with patient recruitment and follow-up
📅 Managing study schedules and visit timelines
📊 Ensuring data accuracy and completeness
The CRC ensures that clinical trials are conducted ethically, efficiently, and in compliance with applicable regulations.
🌟 Why Choose a Career as a Clinical Research Coordinator?
Clinical research offers a meaningful and rewarding career path for healthcare and life sciences professionals. Here’s why many candidates choose this field 👇
🚀 Growing Career Opportunities
Clinical trials are increasing globally, leading to steady demand for trained CRCs.
🌍 Global Exposure
Clinical research professionals often work on international studies, gaining global experience.
💼 Career Stability
Healthcare and research roles offer long-term career stability compared to many other industries.
📈 Clear Career Growth Path
A CRC can grow into roles such as:
- Senior Clinical Research Coordinator
- Clinical Research Associate (CRA)
- Site Manager
- Clinical Project Manager
- Regulatory Affairs Specialist
🏥 Work Environment & Learning Exposure
Working as a CRC provides valuable exposure to:
✔ Real-world clinical trials
✔ Site management operations
✔ Regulatory compliance practices
✔ Patient safety and ethics
✔ Multidisciplinary healthcare teams
This hands-on experience is extremely valuable for professionals aiming to grow in clinical research and related domains.
🎓 Who Should Apply?
This role is suitable for candidates who:
✔ Have a background in Life Sciences, Pharmacy, Nursing, or Allied Health Sciences
✔ Are interested in clinical trials and research operations
✔ Possess strong communication and coordination skills
✔ Want to work in an on-site clinical research environment
✔ Are committed to learning and professional growth
Freshers with relevant academic exposure as well as experienced professionals passionate about site operations are encouraged to apply.
📩 How to Apply?
Interested candidates should send their updated resume along with a brief cover letter to:
Make sure your application highlights your interest in clinical research, relevant skills, and any prior exposure to clinical trials or healthcare settings.
📝 Final Thoughts
The Clinical Research Coordinator (CRC) role is a vital position within the clinical research ecosystem. It offers an opportunity to work closely with medical professionals, support high-quality clinical trials, and contribute directly to advancements in healthcare 🌱.
If you are detail-oriented, passionate about research, and eager to grow in the clinical research field, this opportunity in Bengaluru could be the right next step in your career.
Don’t miss the chance to be part of meaningful research that impacts patient lives. Apply today and take your clinical research career forward! 🚀
