The Research Coordinator will screen, enroll, and follow study subjects for Phase I, II, III, and IV clinical trials, ensuring protocol compliance and close monitoring while the subjects are on study.
Conducting Clinical Trials
Enrollment of Study Subjects
Follow-Up Procedures
Administrative/Clerical
Minimum High School Diploma or GED required.
Minimum of two (2) years of clinical research experience.
Maintained certification of accreditation (CCRC/IATA/CPR/NIH/CITI) required and will be verified prior to employment.
Exceptional customer service skills.
Strong attention to detail, a willingness to learn & the ability to stay organized.
Ability to perform clinical assessments.
Strong understanding of FDA clinical trial phases I-IV.
Strong understanding of GCP set forth by the ICH.
Proficient knowledge of medical terminology.
Proficient knowledge of Research-related Terminology.
Strong communication skills, both verbal & written.
Proficient computer software and database skills.
Comfortable working in a fast-paced environment.
Very comfortable asking probing questions to patients, if applicable.
Must demonstrate a caring, compassionate, and patient attitude.