When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Clinical Operations Leader / Clinical Trial Manager team members at Parexel average close to 10 years with the company and we are expanding our team. We currently have Home Based Clinical Operations Leader/Clinical Trial Manager positions available in the US. As the Clinical Liaison to the Project Leader, the COL/CTM leads the clinical aspect of the trial and has a direct impact on the projects, teams, and clients, helping to the benefit of the patients we serve. The COL/CTM has overall accountability for the execution of the clinical operations strategy on the Project. They are responsible for coordinating the functional team members and their activities across all geographies, liaising with project leadership and the sponsor to ensure that the Global Research Operations deliverables (timeline, quality, productivity) are met. The COL/CTM may act as Project Leader for projects involving a small number of services, where no Project Leader is assigned. Individuals selected for these roles will provide clinical leadership to project teams and manage the day-to-day clinical operations while striving to achieve operational excellence through on time delivery within budget and to the highest quality with the goal to exceed client expectations. Successful candidates possess a degree in a life science, nursing qualification or relevant experience Minimum of 2 year's of experience leading the clinical operations of clinical trials in a COL, CTM, CPM role within a CRO (preferred) Biotech or Pharma company required. Prior monitoring experience (preferred) or clinical trial coordination as well as experience leading cross functional groups. To excel in these roles, you need to be detailed-oriented, computer proficient and possess superior interpersonal, organizational and leadership skills. EEO Disclaimer Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Headquartered near Boston, Massachusetts and in Durham, North Carolina, Parexel has over 16,000 employees, with offices that support clients in over 100 countries around the world. We provide the most comprehensive drug development capabilities of any CRO worldwide. Our global regulatory expertise, Phase I-IV clinical research services, and advanced commercialization services all work together to move you through the development journey more smoothly and cost-effectively from beginning to end.