Job Summary

Seeking enthusiastic candidates to support clinical trial activities, monitor study progress, verify clinical data, maintain trial documentation, and ensure compliance with regulatory requirements and GCP standards. Suitable candidates should have valuable analytical, communication, and documentation skills.

Qualification & Specifications:

MBBS, BDS ,BHMS ,BAMS, BSMS ,PHARMACY B.Sc/ M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDIAL, B.Tech (Biotechnology/Bio Chemistry).

2025 -2026 passed out

Responsibilities:

- Assist in conducting clinical trials and research studies.
- Maintain clinical trial documentation and study records.
- Collect, review, and manage clinical data.




- Ensure compliance with GCP guidelines and regulatory requirements.
- Coordinate with research teams and investigators.
- Support patient recruitment and follow-up activities where applicable.
- Maintain data accuracy, confidentiality, and quality standards.

Skills:

- Clinical Research fundamentals
- Good documentation skills
- Data management and accuracy
- Communication and coordination
- Analytical and problem-solving skills

For more details contact Nandini - HR

(phone hidden)

📌 Wanted Clinical Research Process Associate- New Delhi (Gurugram)
🏢 Resolve Itech
📍 Gurugram