Are you ready to take the next big step in your clinical research career? If you have 1–2 years of experience and are looking to grow in the pharmaceutical and clinical trials industry, this opportunity could be the perfect fit for you!
A promising opening is now available for the position of Clinical Research Associate (CRA) at Trigen Research.
🧪 What Does a Clinical Research Associate (CRA) Do?
A Clinical Research Associate (CRA) plays a critical role in ensuring that clinical trials are conducted ethically, safely, and in compliance with global regulatory standards such as International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use-GCP.
CRAs act as a bridge between sponsors, clinical sites, and regulatory authorities, ensuring smooth execution of studies and accurate data collection.
📌 Job Details
- Position: Clinical Research Associate (CRA)
- Experience Required: 1–2 Years
- Preferred: Immediate Joiners ⏱️
- Industry: Clinical Research / Pharmaceutical
🔍 Key Responsibilities
📝 1. Site Monitoring
- Conduct site visits to ensure protocol compliance
- Monitor patient safety and trial progress
📂 2. Documentation & Compliance
- Maintain trial records and reports
- Ensure compliance with regulatory standards
🤝 3. Site Coordination
- Collaborate with investigators and site staff
- Provide training on protocols
⚖️ 4. Regulatory Adherence
- Follow ICH-GCP guidelines
- Support audits and inspections
📊 5. Data Verification
- Perform Source Data Verification (SDV)
- Ensure data accuracy and integrity
🎓 Eligibility Criteria
Candidates applying for this role should have:
✔️ Degree in:
- Life Sciences 🧬
- Pharmacy (B.Pharm / M.Pharm) 💊
- Biotechnology
✔️ 1–2 years of clinical research experience
✔️ Knowledge of GCP and clinical trial processes
✔️ Strong communication and organizational skills
🌟 Why You Should Apply
🚀 Career Growth
Work on diverse trials and gain hands-on monitoring experience
🌍 Industry Exposure
Get experience aligned with global clinical standards
🧠 Skill Development
Improve expertise in:
- Clinical monitoring
- Data management
- Regulatory compliance
🤝 Networking
Collaborate with experienced professionals and investigators
📩 How to Apply
Interested candidates can apply by sending their updated resume to:
📧 Email: Contact@trigenresearch.com
💡 Pro Tip:
Make sure your CV highlights:
- Clinical trial monitoring experience
- SDV and site management
- Knowledge of ICH-GCP
⚠️ Important Notes
- Immediate joiners preferred ⏳
- Apply only if you meet experience criteria
- Ensure your contact details are accurate
🎯 Final Thoughts
The demand for skilled Clinical Research Associates is rapidly increasing in India’s pharmaceutical sector. If you already have 1–2 years of experience, this opportunity at Trigen Research can help you accelerate your career and gain valuable industry exposure.
Don’t miss out—apply today and take your clinical research career to the next level! 💼✨
