Job Description

Position Overview:

We are seeking a highly motivated and experienced Clinical Research Coordinator (CRC) to manage and support clinical trials. The ideal candidate will have a strong background in clinical research, patient interaction, data collection, and compliance with regulatory requirements. You will work closely with Principal Investigators (PIs), research teams, and external partners to ensure the successful execution of clinical studies.

Key Responsibilities:

• Oversee daily operations of clinical trials, including patient recruitment, scheduling, and follow-up.
• Ensure adherence to study protocols, GCP, and regulatory guidelines.
• Maintain accurate and complete documentation of clinical trial activities.
• Coordinate and communicate with clinical investigators, study participants, and external vendors.
• Collect, record, and analyze data, ensuring data integrity and regulatory compliance.
• Assist in the preparation of regulatory submissions and reports.
• Participate in training and mentoring of junior staff and new team members.

Qualifications:

• Bachelor’s degree in Life Sciences or related field.
• Minimum 2-3 years of experience as a Clinical Research Coordinator or similar role.
• Strong understanding of Good Clinical Practice (GCP), ICH guidelines, and FDA regulations.
• Excellent organizational, communication, and problem-solving skills.
• Ability to work independently and in a team environment.
• Certification in Clinical Research (CCRC or ACRP) preferred.

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