What are the responsibilities and job description for the Clinical Research Coordinator / Assistant position at NMC Research LLC?
Company Description
NMC Research LLC is a leading clinical research site specializing in conducting high-quality clinical trials across diverse therapeutic areas. Collaborating with pharmaceutical companies, biotech firms, and academic institutions, we aim to advance medical science and improve patient care by bringing innovative treatments to market. With state-of-the-art facilities and a highly skilled team, we prioritize ethical research, regulatory compliance, and a patient-centered approach. NMC Research provides end-to-end clinical trial services, including patient recruitment, site management, and data collection, all focused on producing reliable results. Join our mission to transform healthcare through innovation and excellence.
Role Description
This is a full-time, on-site position located in Tampa, FL for a Clinical Research Coordinator / Assistant. The individual in this role will coordinate and manage clinical trials, ensuring compliance with study protocols and regulatory requirements. Key responsibilities include obtaining informed consent from study participants, assisting with study protocol implementation, maintaining accurate documentation, coordinating patient visits and follow-ups, managing data collection, and collaborating with the research team and sponsors to ensure the smooth execution of clinical trials.
Qualifications
- Proficiency in administering and documenting informed consent processes and ensuring participants’ understanding of study protocols.
- Strong familiarity with research methodologies, clinical protocols, and study implementation procedures
- Knowledge of clinical research experience and expertise in managing clinical trials
- Attention to detail, organizational skills, and the ability to manage multiple tasks with precision
- Excellent communication and interpersonal skills for participant interaction and team collaboration
- Bachelor’s degree in a relevant field or equivalent experience is preferred
- Certification as a Clinical Research Coordinator (CCRC) or similar is a plus
- Familiarity with Good Clinical Practice (GCP) guidelines and FDA regulations
- proficency in English required, Spanish and english would preferred.