Clinical Research Coordinator

About the Role

Become a pivotal member of a mission-focused clinical research organization committed to revolutionizing patient access to innovative therapies. Our client is an expanding clinical research company dedicated to speeding up the development of new treatments for patients battling serious and often incurable diseases. Partnering with top pharmaceutical and biotechnology firms, they bring state-of-the-art clinical trials closer to communities in need.

Key Responsibilities

• Manage clinical trial processes from initiation through completion.
• Assist with patient recruitment, screening, enrollment, and coordination of study visits.
• Keep thorough study records and ensure regulatory compliance.
• Work collaboratively with sponsors, Contract Research Organizations (CROs), investigators, and site personnel.
• Safeguard participant safety, ensure protocol compliance, and maintain data integrity.

Qualifications & Experience

• Minimum of 2 years experience as a Clinical Research Coordinator or Clinical Research Associate.
• In-depth understanding of Good Clinical Practice (GCP) guidelines and clinical trial regulatory standards.
• Strong organizational abilities paired with excellent communication and problem-solving skills.
• Capacity to excel in a dynamic, team-oriented setting.
• Bachelor's degree in a science or health-related discipline preferred.
• Experience in startup environments is an advantage.

Why Join Us?

• Contribute meaningfully to patients' lives through clinical research efforts.
• Be part of a rapidly growing company with a clear, ambitious mission.
• Collaborate with seasoned clinical research experts and industry-leading partners.
• Engage with a varied range of innovative clinical studies.
• Advance your professional journey in an organization where your contributions directly promote the development of new therapies.