What are the responsibilities and job description for the Experienced Clinical Research Coordinator position at Hillcrest Medical Research?
Hillcrest Medical Research specializes in conducting Phase I-IV clinical trials, evaluating the safety and efficacy of innovative medications and devices developed by pharmaceutical and biotech companies. We are a trusted site management organization that provides experienced study coordinators to support investigators, sponsors, and patient recruitment. Our extensive network of independent physicians practicing in community settings ensures access to a large pool of eligible trial participants, enabling rapid enrollment. Committed to patient-centered care, we strive to offer groundbreaking medical treatment while adhering to the highest Good Clinical Practice standards.
This is a full-time, on-site role located in DeLand, FL. The Experienced Clinical Research Coordinator will manage the daily conduct of clinical trials, including screening and recruiting participants, ensuring compliance with study protocols, maintaining study documentation, and coordinating with investigators and sponsors. Additional responsibilities include scheduling visits, collecting and recording data accurately, and ensuring adherence to ethical guidelines and regulatory standards.
- Experience in clinical trial coordination, patient recruitment, and protocol compliance
- Ability to maintain accurate study documentation and manage data collection
- Strong organizational and time management skills for scheduling and execution of study visits
- Knowledge of Good Clinical Practice (GCP) guidelines, FDA regulations, and ethical research principles
- Excellent communication and interpersonal skills for interaction with study participants, investigators, sponsors, and team members
- Proficiency in relevant software for data entry and clinical trial management systems
- Detail-oriented with critical thinking and problem-solving abilities
- Healthcare or clinical research certification is a plus