Clinical Research Coordinator

Fortis; Gurugram District; On-site; INR 550,000 - 650,000; Full time

Job summary

Fortis in Gurugram is seeking a Clinical Research Coordinator to support end-to-end trial activities within a regulated environment. You will coordinate trials, develop study documents, and collaborate with investigators, data managers, and medical writers to ensure timely progress and data quality.

The role requires strong knowledge of GCP, excellent communication, and the ability to work independently as part of a cross-functional team.

Qualifications

• Bachelor's degree in life sciences or a related field.
• Proven experience in clinical research coordination, preferably in a pharmaceutical or CRO setting.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Excellent communication, organizational, and problem-solving skills.
• Ability to work independently and as part of a team.
• Proficient in using clinical trial management systems (CTMS) and other relevant software tools.

Responsibilities

• Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory requirements and company policies.
• Develop and maintain study protocols, case report forms, and other study-related documents.
• Collaborate with cross-functional teams, including investigators, data managers, and medical writers.
• Ensure timely and accurate reporting of study progress and results.
• Manage and resolve issues related to study conduct, data quality, or patient safety.
• Maintain accurate and up-to-date records of study activities and participants.

Skills

Communication

Organization

Problem-solving

Teamwork

Education

Bachelor's degree in life sciences

Tools

CTMS

Job description

• Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory requirements and company policies.
• Develop and maintain study protocols, case report forms, and other study-related documents.
• Collaborate with cross-functional teams, including investigators, data managers, and medical writers.
• Ensure timely and accurate reporting of study progress and results.
• Manage and resolve issues related to study conduct, data quality, or patient safety.
• Maintain accurate and up-to-date records of study activities and participants.

Job Requirements

• Bachelor's degree in life sciences or a related field.
• Proven experience in clinical research coordination, preferably in a pharmaceutical or CRO setting.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Excellent communication, organizational, and problem-solving skills.
• Ability to work independently and as part of a team.
• Proficient in using clinical trial management systems (CTMS) and other relevant software tools.