Clinical Research Coordinator

Fortis; New Delhi; On-site; INR 600,000 - 900,000; Full time

Job summary

Fortis is seeking a Clinical Trials Coordinator to oversee trials from initiation to completion, ensuring adherence to regulatory requirements and internal policies. You will develop study protocols, CRFs, and essential documents, while collaborating with investigators, data managers, and medical writers to drive timely reporting and data quality.

The role requires a life sciences degree and proven experience in clinical research coordination, ideally within pharma or CRO settings.

Qualifications

• Excellent communication, organizational, and problem-solving skills.

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 skills

Organizational skills

Problem-solving skills

Education

Bachelor's degree in life sciences or related field

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.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.