The Clinical Trials Office, BMT Research program is looking for a Research Coordinator I.
Will prepare patient/participant documents for study visits, including proofing for data entry errors.
Assist with the preparation and submission of documents to the IRB and study coordinators.
Recruits and conducts informed consent with study participants.
Review consent forms and follow-up procedures with potential study participants if applicable.
Verify the accuracy and complete of documentation.
Will interact directly with patients, managers and other department personnel.
Credentials and Qualifications:
High School diploma with 2 years of relevant experience
To create a Moffitt culture of diversity and inclusion as we strive to contribute to the prevention and cure of cancer.
Moffitt Cancer Center is recognized as the model wherein the diversity of our employees and communities is valued and supported as essential components to contributing to the prevention and cure of cancer.
The cancer center is an equal opportunity employer. It is the policy of the cancer center to prohibit unlawful discrimination and harassment of any type and to afford equal employment opportunities to workforce members and applicants, regardless of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, marital status, disability, genetic information, veteran’s status or any other characteristic protected by federal, state or local law.