Clinical Research Coordinator, RN

START Center for Cancer Research; Miami (FL); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Comprehensive health coverage

401(k) plan with employer matching

Life and disability insurance

Health savings and flexible spending

Paid time off and flexible schedule

Remote work options

Job summary

The START Center for Cancer Research in Miami, FL is seeking a Clinical Research Coordinator, RN to support early-phase oncology trials under supervision of senior staff. You will ensure accurate conduct, adherence to protocols, regulatory requirements, and patient safety, with direct patient interaction, data collection, and protocol-specific activities.

Typical schedule is Monday–Friday 8:00am–5:00pm at 13400 SW 120th St., Suite 300-A, Miami, FL 33186, and you will collaborate with

Qualifications

• RN license in state practicing is required.
• Minimum 2 years of clinical research experience.
• Basic understanding of oncology clinical trials, especially Phase 1.

Responsibilities

• Communicate with sponsors, CROs, and staff about protocol status.
• Monitor day-to-day conduct of studies to ensure protocol and GCP compliance.
• Prepare source documents and manage case report forms.
• Assist with patient screening, consent, and eligibility determinations.
• Support data coordination and reporting, including SAE submissions.

Skills

RN license

Clinical research experience

Oncology trial knowledge

Phase 1 trial understanding

Education

Associate's degree in Nursing

Bachelor's degree in Nursing

Job description

The START Center for Cancer Research ("START") is the world’s largest early phase site network, fully dedicated to oncology clinical research. To date, over 45 therapies conducted at START locations have obtained FDA/EMA approval.

The START Center for Cancer Research is seeking a Clinical Research Coordinator, RN. The Clinical Research Coordinator, RN will work under the guidance of senior research staff to support the daily activities of early phase oncology clinical trials. The CRC, RN ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards. This role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP). The Clinical Research Coordinator will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial. Also, this role is responsible for implementation as well as completion of protocol specific requirements, providing accurate, up to date information to all team members involved with any aspect of carrying out protocol specific requirements.

Work Schedule: Monday-Friday 8:00am-5:00pm

Work Location: 13400 S.W. 120th St, Suite 300-A, Miami, FL 33186

Essential Responsibilities

• Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol.
• Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study.
• Create/review forms created or revised for assigned trials to assure protocol compliance.
• Maintain files using standardized study document labeling and filing procedures.
• Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
• Maintain an up-to-date contact list.
• Assist with patient screening and determination of eligibility.
• Facilitate the informed consent process ensuring that consent is appropriately completed.
• Prepare and manage source documents according to standard operating procedures.
• Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations.
• Assist data coordinator team with case report form completion and query resolution.
• Work with the Principal Investigator to complete and submit Serious Adverse Event reports.
• Perform protocol specific closeout related activities in conjunction with the data coordinator.
• Provide documentation for all deviations whether related to the protocol or a SOP.
• Ensure that all team members involved understand and adhere to assigned protocols.
• Perform telephone triage assessments of patients on trial when necessary.
• Provide patient education regarding participation in a clinical trial, chemotherapy/biotherapy/investigational agent administration and potential side effects.

Required Education and Experience:

• Associate’s degree in Nursing.

• RN license in state practicing.

• 2 years of clinical research experience.

• Basic understanding of oncology clinical trials, particularly Phase 1 studies

Preferred Education and Experience:

• Bachelor’s degree in Nursing.

• Experience working in an oncology setting.

Physical & Travel Requirements:

• Approximately 80% of time is spent sitting.

• Very fast-paced and ever-changing healthcare environment.

• Demanding deadlines and time frames.

• Constant demand for updating knowledge.

• Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.

Best-in-Class Benefits and Perks

We value our employees’ time and efforts. Our commitment to your success is enhanced by a competitive compensation, depending on experience, and an extensive benefits package including:

• Comprehensive health coverage: Medical, dental, and vision insurance provided
• Robust retirement planning: 401(k) plan available with employer matching
• Financial security: Life and disability insurance for added protection
• Flexible financial options: Health savings and flexible spending accounts offered
• Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
• Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

More about The START Center for Cancer Research

Deeply rooted in community oncology centers globally, The START Center for Cancer Research provides access to specialized preclinical and early-phase clinical trials of novel anti-cancer agents. START clinical trial sites have conducted more than a thousand early-phase clinical trials, including for 43 therapies that were approved by the FDA. START represents the world’s largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world.

Ready to be part of a team changing the future of cancer treatment?

Learn more atSTARTresearch.com.

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.