Clinical Research Coordinator

Company DescriptionSpectra Medica is a specialized Clinical Research Organization (CRO) dedicated to advancing medical science through innovative clinical development solutions. We provide expertise in regulatory strategy, protocol development, safety oversight, and clinical trial execution for life-science companies. Our focus includes clinical planning, pharmacovigilance, FDA communication, and site-level execution, ensuring seamless and efficient trials. With a commitment to quality and innovation, our team collaborates with scientific and medical professionals to enhance therapeutic advancements and bridge gaps in clinical research.Role DescriptionThis is a contracted position, remote, for a Clinical Research Coordinator. The responsibilities include overseeing the implementation and administration of clinical trials, ensuring adherence to study protocols, maintaining participant records, and managing informed consent processes. The coordinator will also monitor trial progress, liaise with clinical teams, and ensure compliance with regulatory and ethical standards to deliver high-quality data.QualificationsExperience with Informed Consent protocols and processes.Proficiency in developing, reviewing, and adhering to clinical study protocols.Strong background in Research and Clinical Research Experience.Experience working with and coordinating Clinical Trials, including data management.Strong organizational, problem-solving, and time-management skills.Knowledge of FDA regulations and guidelines applicable to clinical research.Bachelor's degree in life sciences, nursing, or a related field preferred.Professional certification in clinical research (e.g., CCRC, CCRA) is a plus.