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 Treatment Room Nurse-Urology.

The Treatment Room Nurse is responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Treatment Room Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures, standards of practice, and professional evidence-based standards.

Work Schedule: Monday-Friday 8:00am-5:00pm (some flexibility required)

Location: 823 82nd Parkway, Suite B, Myrtle Beach, South Carolina 29572

Essential Responsibilities:

Patient Care

• Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral and intravesical) according to the protocol and applicable regulations.
• Perform study-related activities, including, but not limited to, venipuncture, obtaining blood specimens, IV insertion, venous access device (central line) management, urinary catheter insertion, ECG collection, and vital signs.
• Collect biological samples according to the protocol and Standard Operating Procedures.
• Educate, explain, and inform participants of study procedures.
• Record data obtained according to the protocol and Standard Operating Procedures.
• Use nursing assessment skills to observe participant general well-being and potential adverse events. Document events and take appropriate action as needed.
• Respond to emergency situations based upon nursing standards.
• Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.
• Ensure that the dignity, health, safety, and welfare of participants are given the highest priority at all times.

Planning and problem solving tasks

• Prepare for clinic day ensuring necessary supplies.
• Assist with entry and completion of quality standards for EHR/PQRS.
• Maintain clinic supply inventory.
• Maintain organized storage of clinic supplies and ensure exam/treatment rooms are adequately stocked.
• Place clinic supply orders according to clinic procedures and approved vendor lists.

Communicating tasks

• Assist with the training and mentorship of less tenured staff.
• Communicate with providers regarding a change in patient status.
• Communicate and interact with peers and other departments in a manner that is viewed as having a positive effect on patient services and staff morale. Interact effectively with patients/family members and demonstrate sensitivity in regards to cultural diversity, age specific needs and confidentiality.

Protocol Management tasks

• Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed.

Technical and Quality Tasks

• Use skills, knowledge, nursing diagnosis, and clinical judgement in order to provide a high standard of care for participants in clinical trials.
• Remain current with appropriate emergency certifications and company emergency policy and procedures.
• Able to work effectively and efficiently under tight deadlines, high volumes and multiple interruptions.

Required Education and Experience:

• High School Diploma or GED.
• Licensed Registered Nurse in practicing state.
• Basic Life Support (BLS) certification, an AHA certified program.
• Previous experience in peripheral IV insertion and management of venous access device(s).

Preferred Education and Experience:

• 1 year of experience.
• Oncology Certified Nurse (OCN).
• Clinical Trial and GU oncology experience.
• Experience working with Microsoft Office, including Teams, Excel and Word.
• Advanced Cardiac Life Support (ACLS) Certification, an AHA certified program. Can be obtained within 90 days of hire.
• ONS/ONCC Chemotherapy Immunotherapy Certificate™. Can be obtained within first year of employment.

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 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 at

STARTresearch.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. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 

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.