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.

We are hiring a Clinical Research Coordinator Specialist . The Clinical Research Coordinator (CRC) Specialist serves as a highly experienced and adaptable research professional responsible for leading the operational startup of new START USA sites by providing hands-on coordination and training in Phase I oncology trials. This expert-level coordinator will temporarily fill the CRC role at launch sites, guide and mentor new CRC hires, and ensure the seamless execution of study start-up activities and early operations.

When not deployed for site launches, the CRC Specialist will remotely support existing START sites by covering CRC responsibilities during vacancies, ensuring no disruption in patient care or study conduct. This dynamic role requires advanced knowledge of clinical research, a passion for training and mentoring, and the ability to operate independently in fast-paced, high-stakes environments.

Compensation Range: The anticipated hourly rate for this position is $85,000 to $95,000 annually , depending on experience and qualifications.

Essential Responsibilities

• Act as the interim CRC at new START sites during launch, overseeing study start-up, patient enrollment, and clinical coordination.
• Train and mentor new CRC hires, ensuring adherence to START SOPs, GCP, and protocol-specific requirements.
• Travel as needed (up to 50%) to support site launches and provide in-person assistance.
• Remotely cover CRC duties at existing sites during vacancies, ensuring uninterrupted patient care and study operations.
• Collaborate with leadership on training programs, SOP improvement, and regulatory compliance.
• Communicate effectively with site staff, investigators, sponsors, and patients to uphold study quality and data integrity.

Education & Experience

• High School Diploma or GED required; Bachelor's degree preferred.
• 5+ years of clinical research experience, with deep expertise in Phase I oncology trials.
• Proven record of successfully coordinating multiple complex protocols and mentoring other research staff.
• Exceptional communication, leadership, and training abilities.
• Demonstrated success in implementing quality improvement initiatives or standardization efforts.
• Strong command of clinical trial documentation, patient-facing procedures, and regulatory frameworks.
• Ability to travel up to 50% to various START USA locations as needed.
• Experience using clinical trial management systems (CTMS), EMRs, and sponsor IRT platforms.

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. 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.

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