Clinical Research Coordinator Job Opening

Jobs On The Way; Kamrup Metropolitan; On-site; INR 300,000 - 600,000; Full time

Job summary

Infoclin Consultancy is hiring a Clinical Research Coordinator in Guwahati, Assam. This full-time role involves coordinating daily trial activities, supporting investigators, and ensuring regulatory compliance across study sites.

The position requires a pharmacology degree (M.Pharm/B.Pharm) and familiarity with GCP/ICH guidelines, with at least 6 months of clinical research experience. Travel within Guwahati is expected.

Qualifications

• Bachelor or master degree in pharmacy or related field
• Knowledge of Good Clinical Practice (GCP) and ICH guidelines
• Exposure to clinical trial documentation and patient handling desirable

Responsibilities

• Coordinate daily clinical trial activities at study sites
• Assist investigators during patient screening, enrollment and follow-ups
• Maintain essential trial documents and study files
• Ensure accurate data entry into Case Report Forms (CRFs)
• Schedule patient visits and manage study timelines
• Ensure compliance with GCP, ICH and regulatory requirements
• Act as a liaison between sponsors, monitors and site staff
• Travel to multiple study locations within Guwahati as required

Skills

Clinical research

Regulatory knowledge

Data entry

Education

M.Pharm / B.Pharm

Job description

Are you passionate about clinical research and eager to build a rewarding career in the healthcare and pharmaceutical industry? Do you have hands‑on experience in clinical trials and a desire to work on impactful medical studies? If yes, this opportunity is for you!

A growing clinical research team in Guwahati, Assam is currently hiring an experienced Clinical Research Coordinator (CRC). This position is offered through Infoclin Consultancy, a professional organization engaged in supporting ethical and high-quality clinical research operations across India.

Job Overview

• Job Title: Clinical Research Coordinator
• Employment Type: Full-time

This role is ideal for professionals who want to work at the grassroots level of clinical studies while gaining exposure to multiple research sites across the city.

About the Role

As a Clinical Research Coordinator, you will play a vital role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory guidelines.

You will act as a bridge between:

• Sponsors and Monitors
• Patients and Study Participants
• Regulatory Authorities

This position requires flexibility, strong organizational skills, and a solid understanding of clinical trial processes. Candidates should be comfortable traveling to different locations within Guwahati as per study requirements.

Educational Qualifications

Candidates must meet the following criteria:

M.Pharm or B.Pharm from a recognized institution
Strong foundation in clinical research principles
Knowledge of Good Clinical Practice (GCP) guidelines

Experience Requirements

Minimum 6 months of experience in clinical research preferred
Experience as a Clinical Research Coordinator, CRA trainee, or site coordinator is an advantage
Exposure to clinical trial documentation and patient handling is beneficial

Fresh candidates with relevant clinical research training and strong motivation may also be considered based on skill level.

Key Responsibilities

As a Clinical Research Coordinator, your responsibilities will include:

Coordinating daily clinical trial activities at study sites
Assisting investigators during patient screening, enrollment, and follow-ups
Maintaining essential clinical trial documents and study files
Ensuring accurate and timely data entry into Case Report Forms (CRFs)
Scheduling patient visits and managing study timelines
Ensuring compliance with GCP, ICH, and regulatory requirements
Acting as a point of contact between sponsors, monitors, and site staff
Traveling to multiple study locations within Guwahati when required

Desired Skills & Competencies

Strong communication and interpersonal skills
Attention to detail and excellent organizational ability
Basic understanding of clinical trial phases and protocols
Professional and ethical patient interaction skills
Flexibility to work across different locations in the city
Strong willingness to learn and grow in clinical research

Location Flexibility

This role requires mobility within Guwahati city . Candidates should be open to working at different hospitals, clinics, or research centers as assigned.

Working as a Clinical Research Coordinator opens doors to long-term career growth in the clinical research industry.

With experience, you can progress to roles such as:

Senior Clinical Research Coordinator

Clinical Research Associate (CRA)

Project Coordinator

Clinical Trial Manager

This role offers hands‑on exposure to real‑world clinical trials, patient management, documentation, and regulatory compliance—making it an excellent stepping stone for ambitious professionals.