Associate degree in Health Science or an equivalent combination of related education and experience is necessary.
Minimum 1 year of directly related experience in clinical research and clinical trials is necessary. (Please review SoCRA?s Definition of a Clinical Research Professional for qualifying experience prior to applying.)
or
An advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.
or
Minimum 3 years of human subject experience (clinical, lab or health regulations) such as related patient care, related community health and wellness, related clinical information, and research.
Prior experience collecting and maintaining regulatory documentation;
Proficiency in working with electronic medical records;
Knowledge of and experience with ethical and regulatory aspects of medical research and appropriate conduct of clinical trials, including The Code of Federal Regulations (CFR) and Good Clinical Practice (GCP);
Ability to create source documents, to track protocol-required data points;
Ability to communicate professionally and interact effectively with patients, faculty, staff, and others; team-work is a critical component of this position;
Ability to train others in protocol-required tasks. This could include other coordinators, nursing staff, MAs, etc;
Ability to work independently, think critically, prioritize, and exercise good judgement;
Experience in surgical oncology studies;
- Proficiency with computers, specifically MS Word and Excel;
- Desire to work in a fast paced, patient oriented environment to further scientific knowledge;
- Positive attitude and desire to continually learn and grow professionally.