Research Date Coordinator I

Florida Cancer Specialists•Bradenton, FL

11d•Onsite

About The Position

At Florida Cancer Specialists & Research Institute (FCS), we believe our people are our strength and we invest in them. In addition to having a positive impact on the people and communities we serve, associates benefit from significant professional opportunities, career advancement, training, and competitive wages. FCS has built a national reputation for excellence since 1984. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network, we utilize innovative clinical research, cutting-edge technologies, and advanced treatments to provide world-class cancer care. FCS offers patients access to more clinical trials than any private oncology practice in Florida, including ground-breaking therapies in a community setting. Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States, often leading the nation in initiating research studies and offering new therapies. This role is responsible for the submission of clinical trial data of research studies under the medical supervision of the Principal Investigator (PI) and the research trial supervisor.

Requirements

High school diploma or GED required.
Minimum of two years of medical experience, clinical research experience is highly desirable.
Candidates should have effective communication skills, organized, detail oriented.
Valid Driver’s License, in state of residency, for travel to clinics.
Compliance with the Company’s Driver Safety Operations and Motor Vehicle Records Check Policy is required.
Background, drug, and nicotine screens.
All offers of employment at Florida Cancer Specialists & Research Institute are contingent upon clear results of a thorough background screening.
As a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption.
FCS is a drug-free workplace, and all new hires will be subject to drug/ nicotine testing.
Medical Marijuana cards are not recognized.

Nice To Haves

clinical research experience is highly desirable

Responsibilities

Responsible for the submission of clinical trial data of research studies under the medical supervision of the Principal Investigator (PI) and the research trial supervisor.