Clinical Scheduler

START Research; Miami (FL); In loco; USD 42.000 - 64.000; Tempo pieno

Vantaggi offerti da questo lavoro

401(k) retirement savings plan with 1:

Annual performance bonus

Paid time off and holidays

Medical, dental, and vision coverage

Company-paid life and disability保险

Employee Assistance Program (EAP)

Flexible FSA and HSA plans

Collaborative, inclusive workplace

Descrizione del lavoro

START Research in Miami is seeking a Clinical Scheduler to manage scheduling for protocol-specific studies, including appointments, radiology procedures, and hotel bookings.

The role requires a High School Diploma and at least one year in a healthcare setting, with strong communication and attention to detail.

Competenze

• One year experience in outpatient physician practice or healthcare setting.
• Knowledge of medical terminology as it relates to scheduling study specific procedures (CT/MRI/PET scans, biopsies, eye exams).

Mansioni

• Schedule protocol-specific study appointments, radiology procedures, and hotel stays.
• Ensure prior authorizations are completed.
• Maintain patient EMR including filing, faxing, and copying.
• Communicate with patients and care team in a caring and respectful manner; coordinate patient care.
• Engage in ongoing education to maintain skills and competency.

Conoscenze

Effective communication

Collaborative attitude

Attention to detail

Medical terminology knowledge

Formazione

High School Diploma or equivalent

Strumenti

EMR/EHR systems

Descrizione del lavoro

The START Center for Cancer Research (“START”) is the world’s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering"Hope Through Access"tocutting edgetrials throughout the UnitedStatesand Europe.

We are hiring a Clinical Scheduler who will manage scheduling protocol specific Study Schedules including, but not limited to, scheduling appointments, radiology procedures and booking hotel stays.

Location: 13400 S.W. 120th StSuite 300-AMiami, Florida33186

Work Schedule: On-Site 8am-5pm, Monday-Friday

Essential Responsibilities:

• Perform administrative responsibilities, including, but not limited to, scheduling routine follow-up and treatment appointments, managing external referrals and consults, handling no-shows, answering phone calls, and rescheduling patients.
• Ensure prior authorizations are completed.
• Perform the day-to-day delivery of quality services through consistent application of policies, procedures, protocols, and standards.
• Communicate with patients and visitors in a caring and respectful manner. Collaborate with other care team members and anticipate their needs to ensure coordinated patient care.
• Use and maintain patient electronic medical records, including filing, faxing, and copying.
• Assist with ongoing quality improvements to provide efficient, cost-effective care.
• Engage in continuous education and training to maintain skills, knowledge, and competency to complete functions of role.

Required Education and Experience:

• High School Diploma or equivalent.
• One year experience in an outpatient physician practice or healthcare setting.
• Effective communication skills and collaborative attitude.
• Strong attention to detail.
• Knowledge of medical terminology as it relates to scheduling study specific procedures such as CT/MRI/PET scans, biopsies, eye exams, etc.

Preferred Education and Experience:

• Oncology and/or research experience.

Best-in-Class Benefits and Perks

• 401(k) retirement savings plan with employer match
• Eligibility for an annual performance bonus, based on role and company results
• Generous paid time off and paid holidays
• Comprehensive medical, dental, and vision coverageand optional insuranceoptions
• Company‑paid life and disability insurance for added financial protection
• Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one
• Flexible FSA and HSA plans to support your financial wellness
• Commitment to a supportive environment that values balance, wellbeing, and flexibility
• We’recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you’lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More About START

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”.

Learn more atSTARTresearch.com.

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

Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide.

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.