TalentCraft is currently partnering with a leading healthcare organization who is seeking a motivated and detail-oriented Clinical Research Coordinator to join their growing team in Chicago. In this role, you will assist in the planning, coordination, and execution of clinical research studies, ensuring compliance with regulatory requirements and institutional guidelines. The ideal candidate has 1-2 years of experience in clinical research and is passionate about contributing to advancements in patient care and medical research.
Key Responsibilities:
- Assist with the development, implementation, and management of clinical research protocols.
- Coordinate participant recruitment, screening, enrollment, and follow-up activities.
- Collect and maintain accurate study data in compliance with study protocols and regulatory requirements.
- Collaborate with physicians, investigators, and study teams to ensure smooth study execution.
- Monitor and report any adverse events or protocol deviations to appropriate authorities.
- Ensure study materials are prepared and available, including informed consent forms and regulatory documents.
- Maintain accurate documentation and ensure timely reporting of study progress.
- Coordinate research-related activities between hospital departments, sponsors, and study participants.
- Assist in preparing reports, presentations, and submissions to Institutional Review Boards (IRBs) as needed.
Qualifications:
- Bachelor’s degree in health sciences, nursing, or a related field.
- 1-2 years of experience in clinical research coordination or a related field.
- Knowledge of Good Clinical Practice (GCP) guidelines and FDA regulations.
- Strong organizational and communication skills.
- Detail-oriented with the ability to manage multiple projects simultaneously.
Preferred Skills:
- Previous experience in a hospital or academic research setting.
