Senior Clinical Trial Manager - CNS/Rare Diseases
Senior Clinical Trial Manager - CNS/Rare Diseases Home Based anywhere in US As a CTM you would be expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects Contribute to the development and maintenance of cross functional project management plans Responsible for risk mitigation strategies, associated action plan and issue resolution Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff Provide direction and support to the Clinical Operations study team Collaborate with Business Development (BD) to ensure timely completion of change orders Track Clinical Operations project deliverables using appropriate tools Role Requirements Must have Clinical Trial Manager experience in CNS and/or Rare Diseases University/Bachelor's Degree in medicine, science or equivalent degree/experience. A satisfactory progression of monitoring experience with previous experience in leadership and/or management activities Previous working experience within the clinical trial management field. Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials. Some knowledge of project management processes and tools. Fluent in written and spoken English. Computer literate. Due to the nature of this position it may be required for the employee to travel approx 25%. Therefore, dependent on the employee's location, the employee may be required to possess a valid Driver's license ICON Plc is an equal opportunity employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.