What are the responsibilities and job description for the Clinical Research Coordinator position at Next Code Placement?
Role Description
This is a full-time, on-site position located in New York, NY. The Clinical Research Coordinator will oversee clinical trials, ensuring compliance with protocols and ethical standards. Responsibilities include obtaining informed consent from study participants, managing research activities, coordinating with investigators and staff, and maintaining accurate documentation. The role requires close collaboration with medical and research teams to ensure the successful execution of clinical trials.
Qualifications
- Experience in Clinical Research, including Clinical Trials and managing research activities
- Knowledge of Informed Consent procedures and the ability to implement these processes effectively
- Understanding of Protocol requirements and adherence to regulatory and ethical standards
- Strong organizational, communication, and teamwork skills
- Bachelor’s degree in a related field (e.g., Life Sciences, Healthcare) is preferred
- Prior experience in a healthcare or clinical setting is a plus