Clinical Research Coordinator, RN

START Center for Cancer Research • San Antonio, TX

12d

About The Position

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. We are hiring a Clinical Research Coordinator, RN , supports early phase oncology trials under senior research staff guidance. This role ensures accurate, timely research conduct, adhering to protocols, regulatory standards, and patient safety. Responsibilities include direct patient interaction, data collection, maintaining Good Clinical Practice (GCP), overseeing multiple protocols, and coordinating patient participation. The CRC, RN implements and completes protocol requirements, ensuring accurate, up-to-date information is provided to the team.

Requirements

• Associate’s degree in Nursing and RN license in practicing state
• 2 years of clinical research experience, with a basic understanding of oncology Phase 1 trials.
• Strong attention to detail, accuracy in data collection, and ability to meet deadlines.
• Excellent organizational, time-management, and communication skills.
• Proficient in Microsoft Office Suite, clinical trial management software, and knowledge of GCP and regulatory requirements.

Nice To Haves

• Bachelor’s degree in Nursing.
• Experience working in an oncology setting.

Responsibilities

• Communicate regularly with Study Sponsors, CROs, and staff regarding protocol status, questions, and concerns.
• Monitor day-to-day study conduct to ensure protocol, SOP, and Good Clinical Practice compliance.
• Review and create trial forms to ensure protocol compliance.
• Maintain organized study files with standardized labeling and filing procedures.
• Implement protocols and amendments, training staff on patient treatment and management.
• Assist with patient screening, eligibility determination, and informed consent process.
• Manage source documents, address protocol deviations, assist with case report forms, and submit Serious Adverse Event reports.

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: Associate degree