Research Support Specialist

Date Posted:

2026-08-28

Country:

United States of America

Location:

Broadway Office

WHY JOIN FCS

At Florida Cancer Specialists & Research Institute, 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.

Offering competitive salaries and comprehensive benefits packages to include tuition reimbursement, 401-K match, pet and legal insurance.

A LITTLE BIT ABOUT FCS

Since 1984, Florida Cancer Specialists & Research Institute & Research Institute (FCS) has built a national reputation for excellence. With over 250 physicians, 220 nurse practitioners and physician assistants and nearly 100 locations in our network. Utilizing innovative clinical research, cutting-edge technologies, and advanced treatments, we are committed to providing world-class cancer care. We are recognized by the American Society of Clinical Oncology (ASCO) with a national Clinical Trials Participation Award, FCS offers patients access to more clinical trials than any private oncology practice in Florida. Our patients have access to ground-breaking therapies, in a community setting, and may participate in national clinical research studies of drugs and treatment protocols. In the past five years, the majority of new cancer drugs approved for use in the U.S. were studied in clinical trials with FCS participation prior to approval.

Through our partnership with Sarah Cannon, we are one of the largest clinical research organizations in the United States. Often, FCS leads the nation in initiating research studies and offering ground-breaking new therapies to patients.

Come join us today!

Summary:

Assists investigators and/or other study staff in the implementation, coordination and conduct of clinical research activities. Helps to maintain all research protocol data and compliance reporting.

PRIMARY TASKS AND RESPONSIBILITIES:

• Performs administrative tasks to support investigators and research teams at the Research hubs
• Assists in the preparation of supplies for study visits (consent forms, data collection materials, lab kits, etc.)
• Maintains office inventory and orders necessary supplies.
• Provides assistance in the conduct of site visits/audits by the sponsor or regulatory agencies.
• Assists other internal stakeholders in processes related to archival of closed research studies.
• Participates in continuing education (i.e., meetings, seminars and other activities) as deemed appropriate.
• Order, register, organize, store miscellaneous materials for the clinical sites when needed for treatment appointments.
• Will comply with all federal law and the study sponsors' rules concerning the process of qualifying, receiving, using and accountability of all protocol vendor supplies, per documented standard operating procedures and in agreement with FDA rules and sponsor's procedure as applicable.
• Respects patient rights and protects the confidentiality of patient and organizational confidential information

EDUCATION/CERTIFICATIONS & LICENSES:

• High School diploma or equivalent required.
• Associate's Degree preferred

EXPERIENCE:

• At least two (2) years of medical/clinical work with oncology or clinical research experience preferred
• Proficient with Microsoft Office (Word, Excel, Outlook, PowerPoint)

CORE COMPETENCIES, KNOWLEDGE/SKILLS/ABILITIES:

Essential competencies and KSAs targeted to successfully performing in role:

• Analysis & Critical Thinking
• Strong interpersonal skills to include effective verbal and written communication
• Solid time management with the ability to prioritize multiple tasks
• Ability to collaborate across various levels of management, departments and teams
• Comfortable negotiating problems and exploring solutions with physician population

VALUES:

• Patient First - Keeping the patient at the center of everything we do
• Accountability - Taking responsibility for our actions
• Commitment & Care - Upholding FCS vision through every action
• Team - Working together, one team, one mission

Expectations for all Employees

Every FCS employee is expected to regularly conduct themselves in a professional and respectful manner, to comply with all labor laws, workplace policy and workplace practices. Employees are expected to bring issues of any forms of workplace harassment, discrimination or other potential improprieties to the attention of their management or the human resources department.

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SCREENINGS - Background, drug, and nicotine screens

Safeguarding our patients and each other is an important part of how we deliver the best care possible to the communities we serve. All offers of employment at Florida Cancer Specialists & Research Institute are contingent upon clear results of a thorough background screening. Additionally, as a condition of employment, FCS requires all new hires to receive various vaccinations, including the influenza vaccine, barring an approved exemption. In addition, FCS is a drug-free workplace, and all new hires will be subject to drug/ nicotine testing. Medical Marijuana cards are not recognized.

EEOC

Florida Cancer Specialists & Research Institute (FCS) is committed to helping individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at FCS, please email FCS Recruitment (Recruiter@FLCancer.com) for further assistance. Please note this email address is intended to request an accommodation as part of the application process. Any other correspondence will not receive a response.

FCS is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.