Clinical Trial Assistant

Clinical Trial Assistant (CTA) The Clinical Trial Assistant supports clinical trials by maintaining organized files, performing pharmacy technician duties, communicating routinely with trial sites, coordinators, and patients while demonstrating good clinical practices and following standard operating procedures. Clinical trials are designed to test new medications and medical devices for safety and efficacy. Responsibilities Monitor study activities to ensure compliance with protocols and all relevant local, federal, and state regulatory and institutional policies. Maintain required records of study activity including case report forms, drug dispensation records, and regulatory forms. Order drugs or devices necessary for study completion. Maintain current knowledge of clinical studies affairs and issues by reviewing scientific literature, participating in continuing education activities, and attending conferences and seminars. Prepare for and participate in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups. Organize space for study equipment and supplies. Participate in the development of study protocols including guidelines for administration or data collection procedures. Maintain contact with sponsors to schedule and coordinate site visits or to answer questions about issues such as incomplete data. Identify protocol problems, inform investigators of problems, and assist in problem resolution efforts such as protocol revisions. Dispense medical devices or drugs, calculate dosages and provide instructions as necessary. Perform all other duties assigned. Expectations Understand, organize, and archive clinical trial documents, including study protocols, SOPs, resource documents, dispensing and manufacturing records, email correspondence, training materials, and other study documents. Maintain current lists of correspondence. Administer clinical trials according to good clinical practices and standard operating procedures. Provide general logistical support for clinical trials by entering subject and study site orders and arranging and confirming deliveries of study medications and supplies. Travel may be required. Qualifications Minimum: High School Diploma or GED. Prior work experience in healthcare or life sciences; clinical trial experience preferred. Meticulous attention to detail and a demonstrated willingness to complete routine administrative tasks. Ability to work in a team environment. Excellent written and verbal communication skills. Strong skills in MS Office programs (Excel, Word, PowerPoint). Current State of Missouri Pharmacy Technician Registration required. Preferred: Strong organizational and interpersonal skills. Physical / Mental Demands and Working Environment May be required to reach, grasp, stand and/or sit for long periods; walk, talk and hear; occasionally lift or move up to 25 pounds. The noise level is usually moderately quiet with frequent interruptions and multiple demands. Equal Opportunity Employer EVERSANA is an Equal Opportunity Employer. All employment decisions are made without regard to race, color, religion, national origin, age, disability, veteran status or any other characteristic protected by applicable law. We provide reasonable accommodations for qualified applicants with disabilities under the Americans with Disabilities Act (ADA) and applicable state and local laws. #J-18808-Ljbffr