Advertisement
Are you passionate about advancing oncology clinical trials and ensuring data accuracy in healthcare research? Suma Soft Pvt. Ltd., a leader in IT and clinical data management services, is hiring a Clinical Research Data Coordinator for a full-time night shift role in Pune.
Advertisement
This is an excellent opportunity for candidates with a strong background in clinical research coordination, data management, and protocol compliance. If you thrive in a fast-paced, detail-driven environment and want to make a meaningful impact in healthcare, this role is for you.
🔹 Key Responsibilities
As a Clinical Research Coordinator – Oncology Trials, you will:
- Coordinate oncology research studies with precision and protocol adherence.
- Ensure regulatory compliance and maintain data accuracy across study phases.
- Communicate effectively with sponsors, monitors, and regulatory bodies.
- Resolve data queries and discrepancies to ensure study integrity.
- Manage multiple projects independently in a fast-paced, dynamic environment.
🔹 Qualifications & Skills
- 🎓 Bachelor’s degree in Life Sciences or a related field.
- 🧪 Minimum 2+ years of clinical research experience.
- ✅ CCRC (ACRP) or CCRP (SOCRA) certification preferred.
- 💬 Strong communication, organizational, and critical-thinking skills.
- 👨 Male candidates only.
🔹 Benefits of Joining Suma Soft Pvt. Ltd.
- Work on cutting-edge oncology trials with global exposure.
- Gain experience in clinical trial data management and protocol compliance.
- Competitive salary and growth opportunities.
- Collaborative and innovative workplace culture.
- Opportunity to contribute to life-saving medical research.
📌 Application Process
Ready to take the next step in your clinical research career?
Advertisement
- Apply now by sending your CV to: sakshi.shah@sumasoft.net
Advertisement
