Senior Clinical Research Coordinator - Wilmington, NC

CRC) role at Innovo Research is a pivotal position responsible for managing the daily operations of clinical research studies at a designated partner site. This position involves close interaction with Principal Investigators and clinical teams to ensure that each study is executed efficiently and in adherence to regulatory requirements. The Senior CRC supervises clinical research staff performing clinical functions such as phlebotomy and vital signs monitoring and assists in mentoring and training new clinical research personnel. Managing multiple concurrent clinical trials, this role entails participant screening, recruitment, enrollment, scheduling, data management, and preparation of regulatory documentation including IRB submissions and continuing reviews. The Senior CRC also acts as a liaison with pharmaceutical companies, laboratories, vendors, and equipment suppliers to maintain the necessary resources for study conduct.

Additional responsibilities include supporting the informed consent process, advocating for subject safety throughout the research lifecycle, and facilitating pre-study qualification, site initiation, monitoring visits, and study close-out activities. This position requires meticulous attention to detail to ensure compliance with Innovo policies, institutional, sponsor, and federal regulations. The Senior CRC plays a crucial role in collecting, processing, and shipping laboratory specimens and supporting the maintenance of protocol-related documentation. This role is vital to the success of clinical trials that ultimately contribute to the development of new therapies aimed at improving patient outcomes. Innovo Research offers a dynamic and rewarding environment for clinical research professionals who are passionate about making a positive impact on healthcare through rigorous scientific investigation.
• Bachelor’s degree or equivalent
• Experience in clinical research coordination
• Knowledge of human research subject regulations
• Ability to perform clinical functions such as phlebotomy
• Experience managing multiple concurrent clinical trials
• Strong organizational and communication skills
• Ability to comply with regulatory standards and SOPs