To coordinate and manage clinical studies and site personnel from pre-study planning through successful completion of enrollment.
Previous clinical study experience that developed the necessary skills to manage research projects is required. Additional training in nursing or the health care industry is also recommended.
Participate in proposal and contract development, including protocol assessment, budgeting and resource allocation, and interact with company clients as required to obtain sufficient information for proposal development;
Develop and implement solutions and suggestion for improving outsourcing operational efficiency. Ensure the entire office maintains strict adherence to current protocols, resulting in protocol violations;
Screen and manage additional coordinators and support staff as the company expands and grows;
Explore new business opportunities.
Supervise and manage research staff on a daily basis;
Ensure that all employees are working at their optimum level. Hire and terminate personnel as required;
Ensure training sessions and office audits are being completed as scheduled;
Meet each CRA during their visit to insure coordinating responsibilities are being met. Be present during all discussions between CRAs and Principal Investigators;
Employee evaluations, salary increases and counsel employees when required;
Assist in pre-study planning, including preparation of critical documents, discussing logistics, and subject recruitment strategies. Attendance at pre-study meetings (site visits and initiations) and off-site investigator meetings, as required;
Assist coordinators with daily subject visits;
Ensure smooth subject flow during subject hours;
Maintain and update current and upcoming trial list;
Maintain a calendar, including site visits, study initiation visits, subject stays, monitor visits and staff scheduling;
Assign new studies to coordinating teams;
Attend appropriate professional meetings and review scientific and medical literature to increase research knowledge.
This position reports to the Director of Research Operations. Training and guidance will be provided through regular meetings, phone contacts and travel. There is a high degree of autonomy in this position. Independence in decision making and problem solving is encouraged as well as offering ideas for improving and promoting the company.
About Complete Health
We are an experienced clinical research group, founded in 1998 with locations in Birmingham, Alabama and Volusia County, Florida. Since our inception, Complete Health Research™ has developed a reputation of excellence and trust in the pharmaceutical industry. Our sole focus is on clinical research. This ensures all of our clinical trial partners - Participants and Sponsors- can count on us for quality care, unparalleled service and exceptional performance.
Our mission is to bring clinical research to as many lives as possible, we are partnered with Complete Health, who see the value of clinical research and the benefits of offering it as a care option to the patients for whom they serve. Our experienced team of clinical research professionals prides itself on personalized attention, uncompromised data quality and outstanding patient care which are just a few of our core values.