Contract - Clinical Research Coordinator

Science 37 is accelerating clinical research by expanding patient access to trials, leading to faster approvals and better health outcomes. We are looking for a Clinical Research Coordinator to join our team in a fully remote capacity to help manage study participant recruitment, enrollment, and follow-up processes.

Key responsibilities

• Participate in the implementation and execution of clinical trial activities from study start-up to closure.
• Screen potential participants for protocol eligibility and manage the informed consent process.
• Ensure research quality and compliance with SOPs, GCP, and applicable federal and local regulations.
• Coordinate patient care, monitor participant conditions, and document adverse events in collaboration with investigators.
• Maintain accurate data collection, entry, and reporting while supporting the development of clinical protocols.

Requirements

• Minimum of 5 years of pharmaceutical-sponsored clinical research experience.
• Bachelor’s degree or an equivalent combination of education and professional experience.
• Expert knowledge of FDA regulations, GCP guidelines, and HIPAA requirements.
• Strong communication skills with the ability to interact compassionately with patients and caregivers.
• Proficiency in MS Office, Google Suite, and the ability to work effectively in a decentralized team environment.

What we offer

• Opportunity to work in a pioneering company focused on decentralized clinical trials.
• Collaborative environment with cross-functional teams and mentorship opportunities.
• Potential for conversion to a full-time role after 6 months of contract work.