Mount Juliet, Tennessee, United States
I am a dedicated professional in oncology research, currently serving as the Manager of Study Activation. My role involves overseeing the start-up of clinical trials across a network of clinics nationwide, ensuring that each trial is efficiently and effectively initiated. With a strong background in biology and a passion for leadership, I bring both technical expertise and authentic leadership to my team. As a Manager of Study Activation, I lead a team responsible for the critical phase of clinical trial start-ups. My leadership style is characterized by candor and authenticity, fostering a collaborative and transparent environment. I am committed to advancing cancer research and improving patient outcomes through meticulous planning and execution of clinical trials. Skills and Expertise - Leadership and Team Management: Proven ability to lead and inspire teams, driving performance and fostering a positive work culture. - Clinical Trial Activation: Expertise in the start-up processes of clinical trials, ensuring compliance and efficiency. - Technical Knowledge: Strong foundation in biology, enabling a deep understanding of the scientific aspects of oncology research. - Strategic Planning: Skilled in developing and implementing strategies that align with organizational goals and enhance research outcomes. - Communication: Effective communicator, adept at conveying complex information clearly and persuasively.
As the Manager of Study Activation, I lead a dedicated team responsible for the successful initiation of clinical trials. My role involves establishing effective working relationships with senior management, program management, site support operations teams, principal investigators, study teams, sponsors, and other external consultants. I am committed to driving improvement strategies and ensuring high-level service and collaboration with our site, sponsor, and CRO partners. Key Responsibilities - Overseeing the study activation team and ensuring efficient trial start-ups. - Liaising with site, sponsor, and CRO contacts to maintain organizational connectivity. - Facilitating business development and relationship management activities. - Utilizing metrics to drive improvement strategies for trial activations. - Providing oversight, leadership, and direction in study start-up and maintenance areas. - Assessing and streamlining organizational processes associated with start-up and support. - Keeping executive and management teams informed of issues, progress, and risks related to study start-up. - Developing and implementing programs to promote recruitment, retention, and continuing education of teams.
As a Senior Study Activation Specialist at Sarah Cannon Research Institute, I led a team of Study Activation Specialists, overseeing the activation of complex and high-priority clinical trials. In addition to my previous responsibilities, I managed more challenging trials and projects, ensuring efficient coordination with Strategic Sites, physicians, CROs, and Pharmaceutical Companies. I facilitated site and sponsor calls, streamlined trial start-up processes, and provided expert resolutions to expedite study activation. My leadership role involved mentoring team members, developing best practices, and maintaining strong relationships with research staff, physicians, and industry partners. I tracked site metrics, coordinated study supply shipments, and ensured comprehensive protocol training for strategic sites.
As a Study Activation Specialist at Sarah Cannon Research Institute, I was the primary point of contact for clinical trials, coordinating with Strategic Sites, physicians, Contract Research Organizations (CROs), and Pharmaceutical Companies. My role involved driving the trial activation process from site selection and document collection to activation. I facilitated site and sponsor calls, managed trial start-up processes, and provided resolutions to complex problems to expedite study activation. Additionally, I developed and maintained strong relationships with research staff, physicians, and industry partners, ensuring all necessary actions were completed for trial activation. My responsibilities included tracking site metrics, coordinating study supply shipments, and ensuring protocol training for strategic sites.
As a Compounding Process Technician, I compounded pharmaceutical solutions for phases II and III of clinical trials, adhering to GMP standards. I collaborated with process development teams to create scalable processes that improved yield and reduced costs. My responsibilities included conducting inventory management using SAP and delegating tasks to optimize manufacturing processes and meet regulatory requirements.
As the Assistant General Manager of Firehaus, I played a key role in overseeing daily operations, ensuring exceptional customer service, and maintaining high standards of quality and efficiency. I managed staff scheduling, delegated tasks, and supported team development to optimize performance. My responsibilities included inventory management, cost control, and collaborating with the General Manager to implement strategic initiatives that enhanced the dining experience and boosted profitability.