Wanted Clinical Research Process Associate- New Delhi

Resolve Itech Corp; Dadri, New Delhi, Gurugram District; Sur place; INR 350 000 - 520 000; Plein temps

Résumé du poste

Resolve Itech Corp in India seeks enthusiastic candidates to support clinical trial activities, monitor study progress, verify clinical data, and maintain trial documentation in line with GCP standards.

Ideal candidates have strong analytical, communication, and documentation skills, and are prepared to coordinate with researchers, assist in patient recruitment, and ensure data quality throughout the study.

Qualifications

• MBBS/BDS/BHMS/BAMS/BSMS/pharmacy or life sciences degrees required.
• BSc/ MSc in Life Sciences or related fields acceptable.
• Engineering/ biotech degrees also considered.

Responsabilités

• 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, confidence, and quality standards.

Connaissances

Clinical Research fundamentals

Good documentation skills

Data management and accuracy

Communication and coordination

Analytical and problem-solving skills

Formation

MBBS

BDS

BHMS

BAMS

BSMS

PHARMACY

B.Sc Life Sciences

M.Sc Life Sciences

BPT

BE Biomedical

B.Tech Biotech

Description du poste

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 good 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, confidence, and quality standards.

Skills:

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