Clinical Research Coordinator

Why This Role Matters
The Clinical Research Coordinator (CRC) plays a crucial role in ensuring the smooth execution of clinical trials by bridging the gap between investigators, patients, and research teams. This position is essential for maintaining data integrity, patient safety, and regulatory compliance throughout the clinical study lifecycle. Working at a reputed institution like AIIMS Rishikesh offers valuable exposure to clinical research operations and contributes directly to advancements in healthcare and evidence-based medicine.

Job Description
The Clinical Research Coordinator will be responsible for supporting and managing clinical trial activities in accordance with study protocols, regulatory guidelines, and institutional policies. The role involves coordinating with investigators, managing study documentation, ensuring accurate data collection, and facilitating communication among stakeholders. The candidate will also play an important role in patient recruitment, informed consent processes, and maintaining compliance with Good Clinical Practice (GCP) standards.

Key Features of the Role
• Opportunity to work in a premier government medical institute
• Direct involvement in clinical research and patient-centered studies
• Exposure to regulatory compliance and ethical research practices
• Hands-on experience with clinical trial documentation and coordination
• Stable role with scope for learning and professional development

Responsibilities
• Coordinate and manage day-to-day clinical trial activities as per protocol
• Assist investigators in patient recruitment, screening, and enrollment
• Ensure proper informed consent is obtained and documented
• Maintain accurate and up-to-date study records and case report forms (CRFs)
• Monitor patient visits, follow-ups, and study timelines
• Ensure compliance with GCP, ICH guidelines, and institutional policies
• Handle regulatory documentation and assist during audits or inspections
• Communicate effectively with sponsors, CROs, and internal teams
• Maintain confidentiality and ensure data integrity throughout the study
• Support reporting and documentation of adverse events and study outcomes

Required Qualifications
• Any Degree, M.Pharm, or M.Sc Nursing from a recognized institution
• Basic understanding of clinical research processes and regulations
• Knowledge of GCP guidelines and ethical practices is preferred

Educational Requirements
• Bachelor’s Degree in Life Sciences / Pharmacy / Nursing or related field
• Postgraduate qualification (M.Pharm / M.Sc Nursing) preferred

Experience and Skills
• Freshers or candidates with relevant clinical research exposure can apply
• Strong organizational and documentation skills
• Good communication and interpersonal abilities
• Ability to coordinate with cross-functional teams
• Attention to detail and ability to manage multiple tasks
• Basic computer knowledge for documentation and reporting

Age Eligibility
• Minimum Age: 21 Years
• Maximum Age: 45 Years
• Age relaxation applicable as per government norms

Salary Insights
• Basic Pay: ₹27,000 per month
• Opportunity to gain experience in a reputed government healthcare institution
• Valuable exposure to clinical trials and research methodologies

Company Overview
AIIMS Rishikesh is one of India’s leading medical institutions, known for excellence in healthcare, medical education, and research. The institute plays a significant role in advancing clinical research and providing high-quality patient care. Working here offers a structured environment with strong academic and clinical exposure.

FAQs
• Who can apply for this role?
Candidates with a degree in Life Sciences, Pharmacy, or Nursing can apply.

• Is prior experience mandatory?
No, freshers with relevant knowledge or interest in clinical research can apply.

• What is the key responsibility in this role?
Managing and coordinating clinical trial activities while ensuring compliance.

• What is the salary offered?
The position offers a salary of ₹27,000 per month.

• Is this a permanent role?
This depends on the project or contractual terms defined by the institute.

Application Tips
• Highlight any clinical research, internship, or hospital experience
• Mention knowledge of GCP, ICH guidelines, or clinical trials
• Keep your resume focused on coordination, documentation, and patient handling skills
• Ensure all academic and certification documents are updated
• Apply before the deadline (25 March 2026) to avoid missing the opportunity

Application Deadline: 25-03-2026

Official Notification Click Here