Final answer:
A clinical trial coordinator is responsible for managing every aspect of a clinical trial, from scheduling to documentation and working with medical staff. They may have a science background such as a nursing degree and often work in hospitals, but can also be employed by clinics and doctors' offices.
Step-by-step explanation:
Management in the context provided refers to the role of a clinical trial coordinator, who is vital in managing the logistics and operations of clinical trials. This individual's responsibilities include the coordination of patient schedules, appointment setting, maintaining meticulous records, and developing databases for patient tracking, especially necessary for longitudinal studies.
A clinical trial coordinator must ensure that all documentation is thoroughly gathered and adhered to, and they work closely with medical professionals such as nurses and doctors to facilitate the clinical trial and aid in the eventual publication of the research findings.
Candidates for this position often come from a scientific background, such as a nursing degree or other relevant healthcare certifications. Experience working in scientific laboratories or clinical settings can also be valuable. While these positions are commonly found in hospitals, opportunities also exist in various clinics and doctors' offices that conduct clinical trials.