Clinical Research Coordinator Job in Sapientia Medicus Research | Apply Now

Sapientia Medicus Research Inc, a global leader in Site Management Organization (SMO) services, is hiring a Clinical Research Coordinator in Ahmedabad, Gujarat. This full-time, on-site opportunity is ideal for candidates looking to grow in clinical trials, GCP-compliant research, and clinical data management.

With active expertise across oncology, ophthalmology, nephrology, and emerging therapeutic areas, this organization is known for rapid patient recruitment, accurate data collection, and strict GCP adherence. If you’re passionate about advancing clinical research and want to work with international sponsors and investigators, this role is an excellent fit.

Key Responsibilities

• Coordinate day-to-day activities of clinical trials across assigned study sites.
• Ensure informed consent procedures are followed as per ethical and regulatory guidelines.
• Maintain accurate, complete, and timely clinical research documentation.
• Ensure strict protocol adherence throughout trial execution.
• Support investigators, sponsors, and CRO teams during site visits and monitoring.
• Manage patient recruitment, follow-up, and study scheduling.
• Ensure compliance with GCP, ICH, and local regulatory requirements.
• Prepare and maintain essential documents, logs, and regulatory binders.

Required Qualifications

• Strong experience in clinical research, especially in clinical trial coordination.
• Expertise in protocol adherence, informed consent, and GCP compliance.
• Degree in Life Sciences, Nursing, Pharmacy, or related fields preferred.
• Excellent communication, organization, and documentation skills.
• Ability to work independently as well as collaboratively with diverse study teams.
• Experience in site coordination, patient management, and regulatory support is highly desirable.

Preferred Skills

• Knowledge of ethical guidelines, ICH-GCP, and local trial regulations.
• Prior experience working with SMOs, CROs, or investigators.
• Strong problem-solving ability and attention to detail.

Benefits

• Work with an international SMO supporting global multi-centric studies.
• Opportunity to build a long-term career in clinical research operations.
• Exposure to diverse therapeutic areas including oncology and ophthalmology.
• Skill development through collaboration with global sponsors and investigators.

How to Apply

Application Link