Clinical Trial Manager - Central Midwest

Benefits

Qualifications

• •Ability to work in a smaller team environment with a willing, all hands on deck attitude
• •Ability to manage multiple tasks and be comfortable working in an environment with shifting priorities
• •High attention to detail, accuracy, and quality and able to effectively prioritize multiple projects
• •Knowledge of ICH Guidelines, US FDA, and European clinical trial requirements and regulations
• •Excellent written and oral English communication skills required
• •Proficiency in computer programs and specifically in Microsoft office tools including Word, Excel and PowerPoint
• •Bachelor’s degree in science or health related field
• •Demonstrated 5 years minimum relevant experience required
• •Travel required: up to 25%
• •6 more items(s)

Responsibilities

• •Heartflow is the first AI-driven non-invasive integrated heart care solution across the CCTA pathway that helps clinicians identify stenoses in the coronary arteries (RoadMap™Analysis), assess coronary blood flow (FFRCT Analysis), and characterize and quantify coronary atherosclerosis (Plaque Analysis)
• •The CTM will interact well with the Heartflow Clinical Research staff and collaborate effectively with Heartflow onsite and field staff, clinical research coordinators, principal investigators, and vendors to aid in ensuring clinical studies meet or exceed timelines and maintain high quality standards
• •The CTM will have demonstrated experience with clinical research study execution, exceptional organizational skills, excellent attention to detail, and will be comfortable working in a fast- paced start-up culture
• •Participates in clinical research activities including management of clinical study sites, management of study documentation, vendor management, and completion of project management tasks
• •Develops clinical trial timelines, enrollment projections, and instructional materials in support of trial execution, including project, communication, monitoring, recruitment, risk mitigation, and contingency plans
• •Participates in and leads process improvement activities within the department and cross functionally, including SOP development
• •Conducts study start-up activities including the development of protocols, informed consent forms, source document worksheets, training presentations, etc
• •Reviews site regulatory documents (informed consents, IRB approvals, research agreements) to ensure compliance with study requirements and GCPs
• •Maintains effective working relationships with investigators/investigational site research coordinators, and vendors including core labs and data management
• •Perform other duties as required for successfully completing studies, as necessary
• •7 more items(s)