Client Services Coordinator

Charter Research is a highly experienced and quickly growing clinical research company, based in Florida and Illinois, that is looking to add to our team to help us fulfill our mission of discovering future medicines. Our company is privately owned and prides itself on providing exceptional patient experience to our participants, as well as offering agile recruitment strategies to our sponsors. Above all, we are a team, and we are seeking the right team member to add to our foundation in Orlando . POSITION OVERVIEW The Client Services Coordinator is responsible for identifying, tracking, and qualifying potential new study leads and supporting study start-up activities for newly awarded studies for Charter Research sites. RESPONSIBILITIES Maintain extensive knowledge of the capabilities and study needs of Charter Research sites; consistently review the study database and study participant profile of all active and upcoming study protocols, attend relevant meetings, and coordinate with Principal Investigators (PIs) and Clinic Managers. Maintain an internal database of potential upcoming trial opportunities and communicate with the Charter Research team regarding these opportunities through regularly scheduled meetings. Complete and submit feasibility questionnaires/proposals for potential trial opportunities, communicating with the Executive, Medical, Clinical, Marketing, Recruitment, and Finance Teams as needed to respond appropriately to the included questions. Maintain an internal database of current and past completed clinical trials for each site, as well as each PI, to facilitate easy and organized responses to feasibility questionnaires. Review, approve, execute, and submit sponsor and Contract Research Organization (CRO) confidentiality agreements to allow Charter Research to access information regarding potential study opportunities. Schedule and host in-person and virtual meetings to discuss Charter Research’s capabilities and to learn information about potential opportunities, including Pre-Site Selection Visits, Site Selection Visits, and other related capabilities meetings. Document and distribute critical study information needed to inform study acceptance decision-making and study operational planning. Coordinate and support regular study startup activities and meetings with clinical department leadership to gather and document updates, keep the team informed of progress, identify risks and mitigation strategies, and ensure preparedness for study start. Maintain a database of key milestone dates and study startup cycle times (e.g., Study Award to First Patient First Visit/ FPFV) to ensure Charter Research exceeds internal and sponsor or CRO performance standards. Help identify new business opportunities, including studies, indications, and other proposals, by developing and maintaining relationships with sponsor and Contract Research Organization (CRO) contacts and external consultants. Performotherdutiesasassignedorrequired. KNOWLEDGE, SKILLS, AND ABILITIES Exceptionalknowledgeofthedrugdevelopmentprocess. Abilitytohandlemultipletasks/projectssimultaneously. Abilitytocollaboratewithotherteammemberstoachieveresults. QUALIFICATIONS Bachelor’sdegreepreferred. Typically,atleastoneyearofrelatedexperienceinaprofessionalrole,preferablyinaclinicalresearchsetting. PHYSICAL REQUIREMENTS Mustbeabletoliftupto15poundsattimes. Charter Research provides equal employment opportunity (EEO) to all employees and applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability status, genetic information, marital status, ancestry, protected veteran status, or any other characteristic protected by applicable federal, state, and local laws. #J-18808-Ljbffr