Wanted Clinical Research Assistant -Coimbatore

Resolve Medicode; Coimbatore District; On-site; INR 200,000 - 320,000; Full time

Job summary

Resolve Medicode in India is seeking a motivated, detail-oriented fresher to join our Clinical Research team. The role supports trial activities, maintains study documentation, assists with data collection, and ensures regulatory compliance.

You will work under supervision, coordinate with research teams, handle study records, and help with audits. A background in life sciences or health-related degrees is preferred.

Qualifications

• Fresher with MBBS/BDS/BHMS/BAMS/BSMS/Pharmacy or BSc/MSc Life Sciences.

Responsibilities

• Assist in clinical trial and research activities under supervision.
• Maintain and organize clinical research documents and study records.
• Support data collection, entry, and verification.
• Assist in preparing study reports and research documentation.
• Follow clinical trial protocols, SOPs, GCP guidelines, and regulatory requirements.
• Coordinate with research teams, investigators, and other departments.
• Monitor study-related information for accuracy and completeness.
• Maintain confidentiality of patient and study-related information.
• Support preparation for audits and inspections when required.

Skills

Clinical Research fundamentals

Good documentation skills

Data management

Communication and coordination

Analytical and problem-solving

Education

MBBS

BDS

BHMS

BAMS

BSMS

PHARMACY

BSc/MSc Life Sciences

B.P.T

B.E BIOMEDIAL

B.Tech Biotechnology/Bio Chemistry

Job description

Job Summary

We are looking for motivated and detail-oriented fresher to join our Clinical Research team. The candidate will support clinical research activities, maintain study documentation, assist with data collection, and ensure compliance with study protocols and regulatory requirements.

Qualification & Specifications:

MBBS,BDS,BHMS,BAMS,BSMS,PHARMACYB.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

Key Responsibilities

• Assist in clinical trial and research activities under supervision.
• Maintain and organize clinical research documents and study records.
• Support data collection, entry, and verification.
• Assist in preparing study reports and research documentation.
• Follow clinical trial protocols, SOPs, GCP guidelines, and regulatory requirements.
• Coordinate with research teams, investigators, and other departments.
• Monitor study-related information for accuracy and completeness.
• Maintain confidentiality of patient and study-related information.
• Support preparation for audits and inspections when required.

Skills Required

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