Clinical Research Associate at Planet Group Bay County, FL

Clinical Research Associate Clinical Research Associate job at Planet Group. Bay County, FL. Responsibilities This position will include monitoring and oversight of clinical sites to ensure timely and successful execution of clinical studies, resolving study-related discrepancies. Ensure compliance with protocol and all regulatory policies, procedures, and/or guidelines during clinical studies by training/guidance of investigators/study coordinators, and follow-up of corrective actions. Ensure validity of study by identifying/resolving discrepancies and obtaining missing data, and may track more routine aspects of a study of clinical documents, which may include protocols, case report forms (CRFs), memos, correspondence, reports, and other required documents. Conduct new CRA orientation, onboarding, and training activities. Proactively identify and address issues related to study monitoring and clinical site management. Track and communicate monitoring and site management updates and issues; elevate monitoring‑related study timeline and quality risks to the Clinical leadership. Maintain clinical operations processes, new employee onboarding, internal protocol training, monitoring tracking tools, and study tools/templates for CRAs and site personnel. Manage CROs/vendors for outsourced activities as applicable, including sponsor oversight of relevant functional activities (e.g., study management, monitoring, site management, project master files, and data management). Ensure adherence to Good Clinical Practices, industry standards, standard operating procedures, and all other regulatory and quality standards in conducting Lingo Clinical research and development. Operate under minimal supervision and demonstrate a high degree of proficiency. Undertake additional projects and tasks as determined by department and organizational needs. Collaborate across cross‑functional teams, including Quality, Compliance, Product Development, and Engineering. Have prior experience in Clinical Research or Clinical Trials and a solid understanding of related processes. Be a quick thinker, adaptable to evolving workflows, and proactive in seeking clarification when needed. Be resourceful and agile, think critically, adapt to evolving workflows, and proactively seek clarification. Demonstrate creativity in problem solving and openness to exploring innovative ideas and process improvements. Learn internal processes quickly and work independently with minimal supervision. While support is always available, take initiative and adapt quickly in a fast‑paced environment. Qualifications Bachelor's degree – Major/Field of Study: Biology, Health Sciences, Mathematics, Computer Science, or equivalent. Licenses and Certifications: None required; Certified Clinical Data Manager (CCDM) or equivalent nice to have but not required. Compensation Pay ranges between $42‑49/hr based on experience. #J-18808-Ljbffr Planet Group