Job Description

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering access to cutting edge trials throughout the US and Europe. Today, with over 1,300 studies completed, and with research facilities in the United States and in Spain, Portugal, and Ireland, START’s mission is to accelerate the development of new anticancer drugs that will improve the quality of life and survival for patients with cancer and lead to its eventual cure. To date, over 43 therapies conducted at START locations have obtained FDA/EMA approval. Incredibly, while Academic Medical Centers (AMCs) conduct 80% of cancer trials, such trials reach only 20% of the patient population – leaving the majority of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many – by bringing cancer trials to physicians and their patients in community hospitals and practices when hope is needed most.

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. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – the most effective cancer drug in medical history.

Join Our Mission to Transform Cancer Treatment

We are seeking a compassionate and detail-oriented Registered Nurse/Clinical Research Coordinator to join our dynamic Myrtle Beach, SC team. This role offers you the unique opportunity to directly impact cancer research while providing hope to patients in their most vulnerable moments. You'll manage groundbreaking clinical trials across various therapeutic areas, ensuring the highest standards of patient care and scientific integrity.

This is a full-time position with flexible hours in our Monday-Friday office environment, allowing you to maintain work-life balance while making a meaningful difference in patients' lives.

Your Impact as a Clinical Research Coordinator

• Champion patient-centered care while conducting clinical research trials in compliance with GCP guidelines and protocols
• Build relationships with potential study participants, meticulously document medical histories, and maintain accurate records
• Apply your clinical expertise to collect and process lab specimens, manage study drug accountability, and administer medications according to protocols
• Safeguard patient privacy through HIPAA compliance and maintain trial integrity through thorough adverse event reporting
• Orchestrate study-related procedures with precision, ensuring accurate data entry and comprehensive source documentation
• Collaborate with world-class investigators and sponsors to uphold rigorous study standards and quality
• Foster a supportive environment through professional relationships with staff and study personnel

What You'll Bring

• Education: ADN or higher required
• Licensure: Current State of SC nursing license or NLC license from a participating state
• Experience: Minimum of one year working as an RN in a medical setting
• Certification: Basic Life Support (BLS) certification
• Preferred Skills: Experience in urology, oncology, and/or critical care; knowledge of immuno-oncolytics and infusion skills (or enthusiasm to learn)

How We'll Support Your Success

We recognize that exceptional talent deserves exceptional support. Our comprehensive benefits package reflects our commitment to your wellbeing and professional growth:

• Comprehensive health coverage: Medical, dental, and vision insurance
• Robust retirement planning: 401(k) plan with employer matching
• Financial security: Life and disability insurance
• Flexible financial options: Health savings and flexible spending accounts
• Work-life harmony: Generous paid time off, flexible scheduling options

Beyond benefits, we foster a collaborative, innovative environment where you can grow professionally while contributing to our shared mission. Your voice matters here—we encourage participation in our processes, decisions, planning, and culture.

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. Learn more at STARTresearch.com .

Ready to Change Lives Through Groundbreaking Research?

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 today.

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.

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