India’s clinical research industry is on a strong growth trajectory, creating exciting opportunities for life sciences professionals 🚀. One of the most in-demand roles right now is Inhouse Clinical Research Associate (IHCRA). If you have 1–2 years of experience in clinical research, trial documentation, or CRO operations, this role could be the perfect next step in your career.
Currently, Inhouse CRA openings are available across major Indian cities including Kolkata, Mumbai, New Delhi, Hyderabad, Pune, Chennai, and Bengaluru 🌍—metros that offer exposure to global trials, reputed sponsors, and structured career growth.
Below is a clear, publish-ready breakdown of everything you need to know 👇
🔍 What Is an Inhouse Clinical Research Associate?
An Inhouse Clinical Research Associate supports ongoing clinical trials from the office rather than through frequent site visits. Unlike field CRAs, IHCAs focus on documentation, systems management, compliance, and coordination 📑.
This role is critical to ensuring trials are conducted in line with ICH-GCP guidelines, regulatory requirements, and internal SOPs. It’s ideal for professionals who enjoy process-driven work, quality checks, and cross-functional collaboration.
🎓 Eligibility & Experience Requirements
Most organizations look for candidates with:
✔ Background in Life Sciences, Pharmacy, Biotechnology, Nursing, or related fields
✔ 1–2 years of experience in clinical research, CROs, pharma, or healthcare
✔ Exposure to TMF, CTMS, clinical documentation, or trial coordination
✔ Working knowledge of ICH-GCP and Good Documentation Practices (GDP)
Experience as a Clinical Trial Assistant (CTA), TMF Specialist, Study Coordinator, or Inhouse CRA is highly valued.
🧾 Key Responsibilities of an Inhouse CRA
Day-to-day responsibilities are operational and compliance-focused 🧠:
📂 Trial Master File (TMF) Management
Maintain, track, quality-check, and reconcile TMF documents for audits and inspections.
🛡️ Audit & Quality Support
Support internal and external audits by ensuring documentation completeness and SOP compliance.
📄 Essential Document Handling
Coordinate collection, review, and management of essential trial documents, including translations if required.
💻 CTMS Management
Update site milestones, subject data, and compliance metrics in CTMS with high accuracy 📊.
📦 Investigator Site File (ISF) & Logistics
Create and maintain ISFs and coordinate dispatch/tracking of study materials (lab kits, diaries, supplies).
🧪 Study Material & Inventory Control
Ensure safe storage, inventory tracking, and preparation of stock reports for project teams.
🌟 Skills That Make You Stand Out
✨ Strong attention to detail
✨ Clear communication and coordination skills
✨ Ability to manage multiple studies and timelines
✨ Comfort with CTMS/eTMF systems
✨ Solid understanding of regulatory compliance
If you enjoy structured, behind-the-scenes work that supports global trials, this role is a great fit 👍.
💼 Why Choose an Inhouse CRA Role?
Professionals prefer IHCRA roles because they offer:
✅ Better work-life balance than traveling CRA roles
✅ Hands-on exposure to global clinical trial processes
✅ A strong foundation for growth into CRA, Project Management, or Clinical Operations Lead roles
✅ Opportunities with top CROs and multinational sponsors
With India emerging as a global clinical research hub, demand for skilled Inhouse CRAs continues to rise 📈.
📍 Job Locations Available
📌 Kolkata
📌 Mumbai
📌 New Delhi
📌 Hyderabad
📌 Pune
📌 Chennai
📌 Bengaluru
📧 How to Apply
Interested candidates should email their updated CV (MS Word or PDF) mentioning:
📌 Current salary
📌 Expected salary
📌 Notice period
📨 Email: ramesh@thanuassociates.com
🧠 Final Thoughts
If you’re aiming to grow in clinical research without extensive site travel, the Inhouse Clinical Research Associate role is a smart career move. With deep involvement in documentation, systems, compliance, and coordination, this position builds a strong foundation for long-term success 🌱.
Apply now and take the next step in your clinical research journey! 🚀
