Clinical Research Coordinator (CRC)

Why This Role Matters

Clinical Research Coordinators (CRCs) play a crucial role in the successful execution of clinical trials. They help ensure that studies are conducted ethically, safely, and in compliance with regulatory guidelines while supporting investigators, managing documentation, and coordinating with patients and research teams.

Job Description

IQPADS Research is looking for a motivated and enthusiastic Clinical Research Coordinator (CRC) to join their clinical research team in Delhi. This role offers an excellent opportunity for candidates interested in building a career in clinical research and clinical trial management while gaining hands-on experience in clinical trial conduct and site management.

Key Features of the Role

• Position: Clinical Research Coordinator (CRC)
• Company: IQPADS Research
• Location: Delhi, India
• Industry: Clinical Research / Healthcare
• Employment Type: Full-Time
• Salary: As per candidate’s experience, interview performance, and qualifications

Responsibilities

• Coordinate and manage day-to-day clinical trial activities at the site
• Assist investigators in conducting clinical studies according to protocol and regulatory guidelines
• Maintain accurate clinical trial documentation and regulatory files
• Coordinate patient recruitment, screening, and follow-up visits
• Ensure compliance with ICH-GCP guidelines and clinical trial protocols
• Communicate with sponsors, investigators, and site staff to ensure smooth trial conduct

Required Qualification

•BSc , MSc B.Pharm, M.Pharm, Nursing, Biotechnology, or any Life Sciences graduate

Important Requirements

• Minimum 1 year of experience as a Clinical Research Coordinator
• Understanding of clinical trial processes and site management
• Knowledge of ICH-GCP guidelines is an added advantage
• Good communication and organizational skills
• Ability to manage documentation and patient coordination effectively

What We Offer

• Opportunity to gain hands-on experience in clinical research
• Exposure to clinical trial management and regulatory documentation
• Practical learning in patient management and site coordination
• Supportive research team environment

Experience and Skills

• Clinical trial coordination
• Regulatory documentation and compliance
• Patient recruitment and management
• Knowledge of ICH-GCP guidelines
• Communication and organizational skills

Company Overview

IQPADS Research is a clinical research organization involved in conducting and managing clinical trials. The organization focuses on maintaining high standards of research ethics, regulatory compliance, and patient safety while contributing to advancements in healthcare and medical science.

FAQs

1. What is the minimum experience required for this role?
   Candidates must have at least 1 year of experience as a Clinical Research Coordinator.

2. What qualifications are required for this role?
   Graduates in Life Sciences such as BSc , MSc, B.Pharm, M.Pharm, Nursing, Biotechnology, or related fields.

3. Is knowledge of ICH-GCP required?
   It is not mandatory but having knowledge of ICH-GCP guidelines will be an added advantage.

4. How can candidates apply for this role?
   Interested candidates can send their CV via email or message on LinkedIn.

Application Tips

• Highlight your clinical research or CRC experience clearly
• Mention your knowledge of clinical trials and ICH-GCP guidelines
• Include any experience in patient coordination or regulatory documentation
• Emphasize organizational and communication skills